- Open Access
Roles and clinical application of exosomal circRNAs in the diagnosis and treatment of malignant tumors
Journal of Translational Medicine volume 20, Article number: 161 (2022)
Exosomes are microvesicles secreted by cells. They contain a variety of bioactive substances with important roles in intercellular communication. Circular RNA (circRNA), a type of nucleic acid molecule found in exosomes, forms a covalently bonded closed loop without 5′ caps or 3′ poly(A) tails. It is structurally stable, widely distributed, and tissue specific. CircRNAs mainly act as microRNA sponges and have important regulatory roles in gene expression; they are superior to other non-coding RNAs as molecular diagnostic markers and drug treatment targets. Exosomal-derived circRNAs in the body fluids of tumor patients can modulate tumor proliferation, invasion, metastasis, and drug resistance. They can be used as effective biomarkers for early non-invasive diagnosis and prognostic evaluation of tumors, and also represent ideal targets for early precision therapeutic intervention. This review provides a theoretical basis for exploring the applications of exosomal circRNAs in malignant tumor diagnosis and treatment. We describe the biological functions of exosomal circRNAs in the occurrence and development of malignant tumors, their potential utility in diagnosis and treatment, and possible mechanisms.
The occurrence and development of malignant tumors are multifactorial and multi-linked intricate processes. The most important characteristic of malignant tumors is their ability to grow, infiltrate, and diffuse to surrounding tissues without restraint. The morbidity and mortality of malignant tumors are high worldwide and are increasing markedly, representing a non-negligible threat to human health. Most patients are diagnosed at an advanced stage owing to the insidious onset of the disease, which leads to deterioration of their condition and causes them to miss the best time for treatment. Although there has been some progress recently in the diagnosis and treatment of malignant tumors, early diagnosis and effective precision treatment to improve the survival rate remain major challenges in world public health and are key to precision medicine and individualized treatment of malignant tumors. At present, early diagnosis methods and effective treatments are very limited, and the mechanisms of occurrence and progression have not yet been clearly specified. Therefore, it is crucial to explore new non-invasive biomarkers for early diagnosis and treatment of malignant tumors and apply them in clinical practice.
Exosomes, which have an average diameter of 30–150 nm and a double-layered membrane structure, are extracellular vesicles secreted by a variety of cells by exocytosis. Exosomes are important carriers for signaling between cells and are present in body fluids such as saliva, blood, urine, cerebrospinal fluid, and breast milk. Their diverse constituents include almost the entire cell-derived molecular spectrum: circular RNA (circRNA), DNA, mRNA, microRNA (miRNA), proteins, and lipids . Under physiological or pathological conditions, most cells can promote tumor occurrence, development, and metastasis by releasing exosomes containing the above substances into the microenvironment and transferring materials and information between cells.
CircRNAs are important non-coding RNA molecules (ncRNAs) that are produced by alternative splicing of premature mRNAs and usually do not encode proteins. Compared with linear RNAs, circRNAs have stronger stability owing to their characteristic covalently closed loops without 5′ head or 3′ end structures. In recent years, circRNAs have become a hotspot in RNA research. Widely present in eukaryotic cells, they exert specific biological functions by regulating miRNAs and proteins [2, 3] and are closely involved in the occurrence, development, and prognosis of a variety of malignant tumors. Owing to their structural stability, wide distribution, and tissue specificity, circRNAs have advantages over other ncRNAs as molecular diagnostic markers and drug therapy targets. The expression of circRNAs in tumor tissues has been shown to differ significantly from that in normal tissues , indicating that circRNAs could serve as new tumor biomarkers for guiding clinical diagnosis. Known circRNAs can affect the biogenesis of cancers in diverse ways , such as acting as molecular sponges for miRNAs or competing endogenous RNAs (ceRNAs) to regulate the expression of target genes; they can also combine with RNA-binding proteins (RBPs) to regulate the expression of specific proteins, participate in protein translation and other biological functions, and indirectly participate in the occurrence and development of malignant tumors.
Large numbers of circRNAs stably exist in exosomes, which are involved in the composition and regulation of the microenvironment of malignant tumors. The circRNAs are delivered to normal cells via exosomes and have a significant impact on the progression and metastasis of malignant tumors. Recent exosome-related studies have further promoted the clinical translation of circRNAs in oncology, owing to the close connections between circRNAs and exosomes. Here, we summarize the biological functions, roles in diagnosis and treatment, possible mechanisms, and potential applications of exosome-derived circRNAs in malignant tumors.
Structure and biological function of exosome
Exosomes were first identified in sheep reticulocytes and named by Johnstone. Transmission electron microscopy images show that they have a double-layer phospholipid structure with a “spherical” or “cup-like” shape and obvious heterogeneity, and they can be enriched in a concentration gradient of 1.13–1.19 g/ml sucrose solution. Exosomes are biologically active extracellular vesicles that are rich in lipids including cholesterol, ceramide, and sphingomyelin. They contain a variety of functional proteins [e.g., CD9, TSG101, and heat shock protein (HSP70)], DNA, miRNA, lncRNA (long non-coding RNA), and other biologically active substances, which are protected from destruction by being encapsulated in the exosome. The continuous formation process of exosomes mainly involves endocytosis, fusion, and exocytosis, that is, the invagination of the membrane to form a dynamic subcellular structure of multivesicular bodies. These multivesicular bodies have two outcomes: (1) they fuse with lysosomes, and the luminal vesicles are degraded; (2) they fuse with cell membranes, and the tubular vesicles inside depress again to form granular vesicles by endogenous budding and are then released into the extracellular environment in the form of exosomes [5, 6].
Exosomes can be detected in almost all normal and tumor cells and are present in a wide variety of body fluids including saliva, blood, urine, ascites, and breast milk [7, 8]. Their main function is to mediate intercellular communication and material exchange of their contents under physiological and pathological conditions . By transmitting genetic and molecular messages from tumor cells to other cells located at near or distant sites to alter their functional properties and phenotypes , exosomes are also important carriers of specific signals for tumor proliferation, metastasis, immune response, angiogenesis, and drug resistance [10,11,12]. Studies have shown that tumor cells secrete more exosomes whose contents are different than normal cells. Tumor-cell-derived exosomes can provide a suitable microenvironment for tumor development and regulate cell proliferation, angiogenesis, extracellular matrix degradation, metastasis, drug resistance, and the formation of a pre-metastatic microenvironment [13, 14]. Tumor-derived exosomes are mainly composed of ncRNAs, including circRNAs, lncRNAs, and miRNAs. They are considered to be extracellular organelles that play essential parts in remodeling the tumor microenvironment, and represent a new type of non-invasive diagnostic biomarker for tumors . Exosomes have been proved to promote tumor angiogenesis and metastasis during tumorigenesis , contributing to the formation of pre-metastatic ecological niches and the establishment of a suitable microenvironment at distant metastatic sites through stimulating neovascularization, activating mesenchymal stromal cells, and remodeling the extracellular matrix [16, 17]. Tumor-derived exosomes can participate in tumor microenvironment remodeling by releasing cytokines and other bioactive components that act on endothelial cell surface receptors, leading to angiogenesis and promoting tumor metastasis .
Studies have shown the main mechanisms of exosomes function are as follows : direct interaction between exosomes and surface receptors on target cells; cleavage of surface receptors on exosomes and subsequent direct interaction of receptor fragments with receptors on target cells; fusion of exosome membranes with the plasma membrane of target cells, with release of informational material carried by exosomes into the cytoplasm and internalization of the entire exosome through phagocytosis.
Structure and biological functions of circRNAs
Both circRNAs and linear RNAs originate from precursor mRNAs; however, circRNAs are formed by reverse splicing, in contrast to the production of linear RNAs by classical splicing. CircRNAs originate from all regions of the genome, including intergenic, intron, antisense, and untranslated regions. According to their origin, circRNAs can be classified into three major groups: exonic circRNAs, exon–intron circRNAs, and intronic circRNAs. CircRNAs are more stable and less susceptible to degradation by nucleic acid exonucleases than linear RNAs because of their chemical structure of covalent closed loops .
CircRNAs were initially thought to be non-functional byproducts resulting from splicing errors. However, with the development of high-throughput sequencing technology and bioinformatics research, large numbers of circRNAs have been found in mammalian cells, and their structural stability, high conservation, and abundant expression have been demonstrated . The main biological functions of circRNAs: (1) competitive binding with miRNAs to regulate target gene expression; (2) interactions with RBPs to regulate gene expression; (3) regulation of gene transcription or splicing; (4) translation of proteins; and (5) regulation of epigenetic inheritance. Research has shown that circRNAs are related to the pathogenesis of many human diseases and have key roles in tumorigenesis, development, and metastasis; thus, they can be used as effective biomarkers for early diagnosis and prognostic prediction in tumor patients, as well as being ideal targets for early treatment .
Biological functions of exosomal circRNAs
Exosomes are involved in the formation of the tumor microenvironment before metastasis. By mediating immunosuppression and immunosurveillance, exosomes are associated with tumor recurrence and tumor cell survival  Li et al.  found that large numbers of circRNAs were stably present in exosomes derived from various carcinoma cell lines [including laryngeal cancer, oral squamous cell carcinoma (OSCC), thyroid cancer, liver cancer, colon cancer, lung cancer, stomach cancer, and breast cancer] and could be detected in patients’ saliva, serum, urine, and tumor tissues. Various studies have reported that exosomal circRNAs may be related to the occurrence and development of malignant tumors and may regulate tumor cell proliferation, invasion, metastasis, chemotherapy drug resistance, and radiosensitivity.
Regulation of tumor cells proliferation
Dysregulation of proliferation is an important factor in tumor transformation; therefore, the mechanisms of cell cycle regulation have been increasingly brought into focus. Recently, the role of exosomal circRNAs in regulating tumor cell proliferation in various tumors has been gradually elucidated. Exosome-derived circRASSF2 was found to promote the progression of laryngeal squamous cell carcinoma; circRASSF2 expression was significantly higher in tumor tissues than that in control tissues, and downregulation of exosomal circRASSF2 significantly inhibited cell proliferation via the miRNA-302b-3p/IGF-1R axis . In hepatocellular carcinoma, arsenite was shown to induce malignant transformation of human liver epithelial cells (L-02) and cause overexpression of circ_100284, which could be transferred from transformed L-02 cells to normal cells via exosomes. Exosomal circ_100284 accelerated the cell cycle and promoted cell proliferation in normal cells by interacting with miRNA-217. This shows that exosomal circRNAs act as messengers in intercellular communication and suggests a mechanism of arsenite-induced carcinogenesis . Exosomal circDB is upregulated in hepatocellular carcinoma (HCC) patients with high body fat ratio and is transferred to adjacent normal cells with the release of exosomes from malignant transformed cells. It can regulate deubiquitination in HCC by suppressing miRNA-34a and activating the USP7/cyclin A2 signaling pathway, thereby promoting abnormal hepatocyte proliferation and reducing DNA damage . CircIFT80 can promote abnormal proliferation of colorectal cancer (CRC) cells through exosomes, promote DNA synthesis and inhibit apoptosis via the miRNA-1236-3p/HOXB7 axis . CircFMN2 is highly expressed in serum exosomes of CRC patients and its expression levels is negatively correlated with miRNA-1182 levels. CircFMN2 binding to miRNA-1182 can significantly promote CRC cell proliferation, suggesting that exosomal circFMN2 plays a significant part in promoting tumor growth in CRC .
Yu et al. showed that the exosomal circNEK9 accelerated the proliferation, migration, and invasion of gastric cancer (GC) cells by targeting the miR-409-3p/MAP7 axis . CircNRIP1 was significantly upregulated in GC tissues and acted as a miR-149-5p sponge to promote the proliferation, invasion, and metastasis of GC cells; inhibiting circNRIP1 could block the malignant behavior of GC cells via the AKT1/mTOR signaling pathway . Circ_0009910 expression is upregulated in bone marrow, cells and exosomes of acute myeloid leukemia (AML). Inhibiting circ_0009910 can inhibit AML cell proliferation, block the cell cycle, and promote apoptosis. Circ_0009910 regulates AML cell behavior through exosome secretion and the circ_0009910-miR5195-3p/GRB10 ceRNA axis; therefore, circ_0009910 may be an effective target for the treatment of AML . Li et al.  reported that circ_0044516 has a critical role in tumor cell survival and metastasis in prostate cancer. Circ_0044516 has been shown to be significantly upregulated in exosomes and cell lines of prostate cancer patients, and its downregulation inhibits the proliferation and metastasis of prostate cancer cells. Exosomal-derived circ_0044516 may promote prostate cancer cell proliferation by acting as a miRNA-29a-3p sponge. Ma et al.  showed that highly metastatic ovarian cancer EOC cells could transfer their characteristics to cells with low metastatic potential via exosomal circRNA051239, thereby enhancing the proliferation, migration, and invasion capabilities of recipient cells; this indicates a possible mechanism for ovarian cancer treatment.
Regulation of tumors invasion and metastasis
Exosomes can mediate molecular communication and transfer of materials between the primary tumor site and distant metastatic sites, regulate a range of cellular activities including epithelial–mesenchymal transition (EMT), and have crucial roles in invasion and metastasis of tumor cells . Exosomal circ_100338 has been shown  to be involved in the regulation of angiogenesis and metastasis in HCC and is closely associated with the progression of HCC. Transfer of exosomal circRNA-100338 to recipient human umbilical vein endothelial cells (HUVECs) can enhance the metastatic ability of HCC cells, and HUVECs affect pro-angiogenic activity by regulating angiogenesis. HCC cells with high metastatic potential can confer this potential on low-metastatic-potential and non-metastatic cells via exosomes, thereby increasing the invasive and metastatic capacity of these cells. Wang et al.  found that exosomal circPTGR1 contributes to the metastasis of HCC; high expression of circPTGR1 was closely associated with clinical stage and prognosis, and knocking out the expression of exosomal circPTGR1 could significantly inhibit tumor invasion and metastasis in low-metastatic-potential or non-metastatic cell lines. Exosomes from circPTGR1-enriched highly metastatic HCC cells may affect low-metastatic-potential HCC cells by downregulating miR449a-MET interactions in recipient cells, thereby disrupting the homeostasis of the tumor microenvironment and promoting HCC progression.
Given that circPTGR1 is highly abundant and aberrantly expressed in malignant cells and cells from patients with metastasis, it may serve as a prognostic biomarker and therapeutic target for HCC. Circ-0004277 promotes the malignant phenotype of HCC cells by inhibiting zonula occludens 1 (ZO-1) and regulating EMT progression, and stimulates peripheral cells EMT through intercellular communication, further promoting the invasion of HCC to surrounding normal tissues . HCC cells that overexpress circCdr1as can promote the proliferation and metastatic ability of surrounding normal cells through exosome delivery . Wang et al.  showed that exosomes from cholangiocarcinoma cells enhanced the expression of circ-0000284 and stimulated the proliferation and migration of surrounding normal cells. Circ-0000284 can either act as a ceRNA to promote the progression of cholangiocarcinoma, or it can be transferred directly from cholangiocarcinoma cells to surrounding normal cells via exosomes, thereby regulating the biological functions of the surrounding normal cells.
Exosomal circRNAs have significant roles in the progression and metastasis of pancreatic cancer (PC). Exosomal circIARS is widely expressed in PC tissues, where its levels are positively correlated with liver metastasis, vascular invasion, and TNM stage (liver metastasis: P = 0.011; vascular invasion: P = 0.020; TNM: P = 0.023). Circ-IRAS enters microvascular endothelial HUVECs via exosomes from PC cells, downregulates miRNA-122 and ZO-1, upregulates RhoA and RhoA-GTP, increases F-actin expression and focal adhesion, increases the permeability of endothelial monolayer, and promotes tumor invasion and metastasis . Li et al.  showed that exosomal circPED8A was highly expressed in PC tissues and was associated with lymphatic invasion, TNM stage, and low survival rate. CircPDE8A can promote tumor cell growth through upregulating MET. CircPDE8A secreted by tumor cells can be released into the circulation via exosomes, regulate MACC1 as a miRNA-338 sponge, and promote invasion and metastasis through the MET/mitogen-activated protein kinase 1(MAPK1) or protein kinase B pathway.
Exosomal circRNAs can promote GC invasion and metastasis. CircNRIP1 can be transmitted between GC cells via exosomes and affect the Akt1/mTOR signaling pathway as a miRNA-149-5p sponge, thus promoting GC cell metastasis . CircRanGAP1 is significantly upregulated in both cancer tissue and plasma exosomes of GC patients and enhances metastasis and invasion of GC cells via the miRNA-8773p/VEGFA axis . Chen et al. studied exosomes in serum and urine of bladder urothelial carcinoma patients and found that circPRMT5 was significantly upregulated in both sample types ; circPRMT5 could act as a miRNA-30c sponge and promote EMT through the circPRMT5/miRNA30c/SNAIL1/E-calcine mucin 1 pathway. High expression of circPRMT5 in serum and urine exosomes was positively correlated with lymph node metastasis and advanced tumor progression (P < 0.05). Li et al.  showed that FLI1 exon circRNA is a novel oncogenic driver that promotes small cell lung cancer metastasis through the miR584/ROCK1 pathway, and proposed serum exosomal FECR1 as a promising biomarker that could be used to follow the disease progression of small-cell lung cancer. In ovarian cancer, exosomes transfer circPUM1 and circWHSC1 to peritoneal mesothelial cells, thereby promoting tumor metastasis [43, 44]. Studies related to CRC [26, 45] have also identified a role of exosomal circRNAs in promoting tumor invasion and metastasis.
Modulation of chemotherapy resistance and radiosensitivity
Radiotherapy is an important tool for tumor treatment and has a particularly crucial role in the treatment of advanced malignant tumors. However, drug resistance and decreased sensitivity to radiotherapy inevitably occur, leading to tumor recurrence and metastasis [46, 47]; these are the main reasons for failure of tumor treatment and seriously affect treatment effects and prognosis. Therefore, there is an urgent need to overcome tumor drug resistance and enhance sensitivity to radiotherapy. Studies have shown  that exosomes can transmit drug resistance between GC cells. The essential role of circRNAs as the content of chemotherapy resistance transmission is gradually being revealed; for instance, exosomes derived from tumor-associated macrophages were found to transfer miR-21, leading to cisplatin (DDP) resistance in GC. The exosomal circ_0032821 promotes oxaliplatin (OXA) resistance in GC cells via the miR-515-5p/SOX9 axis, suggesting that circ_0032821 is expected to be an effective therapeutic target for GC .
Exosomal circRNAs have a vital role in regulating chemotherapeutic drug resistance and radiosensitivity of CRC. Wang et al.  found that exosomal circ_0067835 inhibited CRC progression and enhanced the radiosensitivity of CRC cells via the miR-296-5p/IGF1R axis. When circ_0000338 was selectively transferred to a co-cultured parental HCT116 cell line (HCT116-P) by exosomes secreted from an OXA-resistant HCT116 cell line (HCT116-R), the viability of HCT116-P cells during drug treatment significantly increased compared with control cells . Malignant tumors usually rely on aerobic glycolysis to produce adenosine triphosphate for rapid growth and resistance to chemotherapeutic agents, and M2-PK has a key role in catalyzing glycolysis. Study has shown  that M2-PK expression is heterogeneous in CRC cells, being higher in OXA-resistant cells and lower in OXA-sensitive cells. miRNA-122 is positively correlated with chemoresistance; exosomes from OXA-resistant cells deliver ciRS-122 to sensitive cells to promote glycolysis and drug resistance by adsorbing miRNA-122 and upregulating M2-PK; this intercellular signaling provides a theoretical basis for the clinical applications of exosomes in drug-resistant CRC.
The exosomal circZNF91 can act as a transporter to mediate signaling between hypoxic and normoxic tumor cells and promote gemcitabine resistance in PC; therefore, it may be an effective therapeutic target . Xu et al.  showed that exosomal hsa_circ_0014235 promotes DDP resistance and development of non-small-cell lung cancer (NSCLC) by mediating the miR-520a-5p/CDK4 pathway. Hsa_circ_0002130 has a promising role as a therapeutic target in osimertinib-resistant NSCLC . Exosome-mediated circ_UBE2D2 has been shown to enhance tamoxifen resistance in breast cancer by binding to miR-200a-3p; this finding provides new insights that could be used to improve the efficacy of tamoxifen in breast cancer patients .
circCdr1as is involved in the formation of DDP resistance in ovarian cancer; functioning as a miRNA sponge to downregulate miRNA-1270 and upregulate suppressor of cancer cell invasion (SCAI), the target gene of miRNA-1270, it can enhance the sensitivity of ovarian cancer cells to DDP. Serum exosomal circCdr1as was found to be abnormally downregulated in a DDP-resistant group compared with the DDP-sensitive group and was significantly negatively correlated with expression levels of miRNA-1270 (r = − 0.679, P = 0.000) . Serum exosome hsa_circ_103801 could serve as a valid prognostic biomarker for osteosarcoma (OS) and may be a potential target for overcoming OS chemoresistance .
Role of exosomal circRNAs in diagnosis and prognosis
A certain amount of progress has been made with respect to the treatment of malignant tumors, for example, in early diagnosis, surgery, and radiotherapy; however, the early symptoms of most tumors are not typical and final diagnosis is difficult as it requires specialized clinicians to obtain samples for processing and to perform complex histopathological biopsies. There is still a lack of rapid, accurate, and non-invasive early diagnostic biomarkers for use in clinical practice. Liquid biopsy based on exosomal circRNAs is a novel method, taking advantage of the fact that circRNAs are enriched in exosomes and have good stability, and that the expression profile of exosomal circRNAs in patients with malignant tumors is different from that in the healthy population . Liquid biopsy can be easily performed using samples of saliva, serum, urine, and other body fluids, avoiding the harm caused to patients by surgery or puncture. As well as its advantages in terms of safety, this method is easier to perform ; it also enables monitoring of the whole process of malignant tumor diagnosis and prognosis evaluation, with strong real-time and timeliness. Thus, exosomal circRNAs have important diagnostic value in a variety of malignant tumors and have great potential as molecular markers for non-invasive early diagnosis and prognostic assessment, thereby providing a new direction for exploration of powerful diagnostic markers for different tumors. Although exosomal circRNAs have great potential to become novel tumor markers, the current understanding of exosomal circRNAs is still in its infancy. Further studies are needed to verify whether the proposed circRNAs have clinical value as tumor markers.
Studies have shown that exosomes are rich in circRNAs with potential biological functions, and human serum exosomes have been proven to contain more than 1000 types of circRNA. This phenomenon is caused by the entry of circRNAs from tumors into the bloodstream . CircRNAs are stably enriched in malignant exosomes, and the transport of circRNAs and other types of molecules by exosomes protects them from degradation and dilution in the cellular extracellular space, resulting in long-distance distribution of circRNAs via the bloodstream or tissue fluid . To detect whether exosomal circRNAs enter the blood circulation and can be quantified for malignancy diagnosis, Xu et al.  analyzed the expression of exosomal circRNAs in serum of endometrial cancer patients and healthy individuals by an RNA sequencing technique. They found that the number of circRNAs upregulated in exosomes of endometrial cancer patients was higher than the number of downregulated circRNAs, indicating that human malignant circRNAs can enter the blood and be easily quantified in serum, and that exosomal circRNAs can affect target cells. These findings may help to identify new mechanisms of malignant tumor development. Li et al.  constructed a mouse tumor model and detected human circRNA-CDYL in serum exosomes; the amount of circRNA-CDYL was closely related to tumor development, further confirming that circRNAs can be used as early diagnostic biomarkers of malignant tumors.
Han et al.  showed that plasma circ_0019201, circ_0011773, and circ_0122790 are potential biomarkers for predicting LSCC. Circ_0019201, circ_0011773, and circ_0122790 were found to be consistent with the training set. The receiver operating characteristic (ROC) curves also showed high diagnostic power, as did the area under the ROC curve (AUC) for both single and combined circRNAs. Circ_0019201, circ_0011773, circ_0122790, and their combinations had AUCs of 0.933, 0.908, 0.965, and 0.990 in the training set and 0.766, 0.864, 0.908, and 0.951 in the validation set.
CircRNAs have a significant role in the development of esophageal squamous carcinoma (ESCC). The expression of serum exosomal hsa_circ_0026611 was found to be significantly upregulated in ESCC with lymph node metastasis ; exosomal hsa-circ-0048117 may have key roles in remodeling the ESCC microenvironment and regulating the progression of ESCC ; and hsa_circ_0001946 shows potential as a good prognostic biomarker . Thus, circRNAs are expected to emerge as new markers for the diagnosis and prognostic assessment of ESCC patients.
In CRC studies, exosomal circRNA levels have been shown to be significantly upregulated in K-ras wild-type CRC DKs-8 cells, suggesting that exosomal circRNA could be used as a biomarker for CRC . Serum exosomal circ_0004771 was found to be significantly upregulated in CRC patients with different TNM stages compared with the control group (P = 0.017), and its AUC for the diagnosis of CRC was 0.88, with a sensitivity of 80.91% and specificity of 82.86%; serum exosomal circ_0004771 in patients with stage I-II CRC was significantly higher than that in normal controls (P < 0.001), and the AUC for the diagnosis of stage I-II CRC was 0.86, with a sensitivity of 81.43% and specificity of 80.00% . Barbagallo et al.  found that serum exosomal circHIPK3 was significantly upregulated in patients with CRC, and the AUC for the diagnosis of CRC was 0.771, with a sensitivity of 71% and a specificity of 80%.
Xie et al.  showed that exosomal circSHKBP1 regulates the miR-582-3p/HUR/VEGF pathway, inhibits HSP90 degradation, and promotes GC progression. CircSHKBP1 is thus a promising circulation biomarker for GC diagnosis and prognosis. Circ-RanGAP1 is significantly upregulated in both GC tissues and plasma exosomes of GC patients and is closely associated with advanced TNM stage, lymph node metastasis, and low survival; therefore, it could be used as a prognostic biomarker and therapeutic target for GC . Shao et al.  found that plasma exosomal circ_0065149 levels in patients with early GC (EGC) were significantly lower than those in healthy controls (P < 0.001), and the AUC for screening for EGC was 0.64, with higher sensitivity (48.7%) and specificity (90.2%) than traditional tumor markers (CEA, CA199, and CA125).
Studies in HCC have confirmed  seven upregulated and five downregulated circRNAs, hsa_circ_0004001, hsa_circ_0004123, and hsa_circ_0075792, which among the upregulated circRNAs, the combination of which can be used as a valuable diagnostic biomarker for HCC. Exosome-derived circ_0051443, which is downregulated in the plasma of HCC patients, inhibited the progression of HCC and had an AUC of 0.8089 for the diagnosis of HCC . Pancreatic ductal adenocarcinoma (PDAC) is among the most aggressive and lethal malignancies, with a 5-year survival rate of only 5% owing to the high risk of metastasis and recurrence. Microarray analysis  showed that circ-PDE8A is a highly expressed circRNA in PDAC and may play a critical part in PDAC invasion; thus, exosomal circ-PDE8A may be an ideal biomarker for early diagnosis or assessment of progression of PDAC. Tumor-derived exosomal circRNA_102481 may promote resistance to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in NSCLC via the miRNA-30a-5p/ROR1 axis. Exosomal circRNA_102481 therefore has potential as a novel diagnostic biomarker and therapeutic target in EGFR-TKI-resistant NSCLC . Exosomal circFARSA plays a crucial part in the interaction between macrophages and NSCLC cells through the PTEN/PI3K/AKT signaling pathway and is a promising diagnostic/prognostic biomarker for NSCLC .
Li et al.  found that expression of serum exosomal FLI1 exonic circRNA 1 (FECR1) was abnormally upregulated in patients with small-cell lung cancer; moreover, higher levels of exosomal FECR1 expression were observed in patients with distant metastases and serum FECR1 levels were closely related to patients’ response to chemotherapy, indicating that FECR1 could be used as a biomarker to assess the progression of small-cell lung cancer. Wang et al.  found that serum exosomal circ_002178 was significantly upregulated in lung adenocarcinoma (LUAD) patients and enhanced expression of programmed cell death ligand 1 (PDL1) by adsorbing miRNA-34 and miRNA-28-5p; circ_002178 showed potential as a non-invasive diagnostic marker for LUAD with an AUC of 0.9967.
Chen et al.  comprehensively analyzed the expression profiles of plasma exosomal circRNAs in LUAD groups and healthy controls and found that the expression levels of circ_0001492 and circ_0001346 were upregulated in early-stage LUAD but almost undetectable in plasma exosomes of healthy controls, suggesting that circ_0001492 and circ_0001346 could be used as novel early diagnostic markers for LUAD. Lin et al.  extended current knowledge regarding the differential expression of circRNAs in plasma exosomes of advanced LUAD, offering prospects for further research on the development and use of biomarkers for diagnosis and prognosis of LUAD. Circ_0102537 was proved to be an effective diagnostic biomarker for advanced LUAD. Chen et al. reported for the first time the altered expression of exosomal circRNAs in plasma samples from LUAD patients, supporting the necessity to explore its usage as a biomarker and its pathological function in lung cancer . Xu et al.  found that circSETDB1 promoted tumor formation through the miR-7/Sp1 pathway. Tumor-secreted circSETDB1 can be released into the circulation via exosomal transport under hypoxic stress, and plasma exosomal circSETDB1 is associated with lymphatic metastasis and T-stage in LUAD patients; thus, it may be an important biological factor in the development of LUAD and is expected to be an ideal biomarker for early diagnosis.
Bioinformatics analysis and real-time fluorescence quantitative polymerase chain reaction technology have been used to show that circ_00005795 and circ_0088088 can compete for endogenous RNAs, and both of these circRNAs were shown to have important diagnostic value in breast carcinoma by comparing the expression of serum exosomal circRNAs in breast carcinoma patients and healthy controls. These results provide a theoretical basis for the occurrence, progression, and metastasis of breast carcinoma [79, 80]. Circ-0001068 is introduced into T cells and induces PD1 expression via exosomes as a ceRNA for miR-28-5p; it represents a novel ovarian cancer biomarker and inducer of PD1 expression in T cells . Targeting exosomal circ-CYP24A1 was found to inhibit the progression of cutaneous squamous cell carcinoma by attenuating the malignant behavior of the tumor . It is thus a promising therapeutic target and non-invasive diagnostic biomarker for cutaneous squamous cell carcinoma.
Luo et al.  showed that circulating exosomal circMYC has great potential as a diagnostic and prognostic biomarker for multiple myeloma. Chemotherapy resistance limits the durability of therapeutic effects and is a major constraint to clinical treatment of oncology. Timely identification of potential drug-resistant patients, monitoring of resistance to chemotherapeutic agents, and finding alternative treatment options are extremely important strategies, enabling treatment to be adjusted and prognosis improved. Exosome-mediated circNFIX enhances temozolomide (TMZ) resistance in glioma by sponging of miR-132 and shows potential as a prognostic biomarker to improve the clinical benefit of TMZ treatment in glioma patients . Exosome-mediated circ-HIPK3 enhances TMZ resistance via modulating the miR-421/ZIC5 axis and promotes tumorigenesis in vitro and in vivo; its expression in serum exosomes can be used as a biomarker for diagnosis of TMZ-resistant glioma .
The roles of exosomal circRNAs in diagnosis and prognostic assessment of malignant tumors are shown in Table 1.
Role of exosomal circRNAs in treatment
The therapeutic delivery of exosomal circRNAs and related genes and proteins as targets can inhibit the proliferation, invasion, and metastasis of malignant tumor cells. This approach can also provide new ideas for therapy of tumors including OSCC , CRC [87, 88], GC , PC , cervical cancer [91, 92], gallbladder cancer , breast cancer , and OS [95, 96]. Exosomes can transport RNA or deliver therapeutic drugs to cancer cells and act as drug carriers for targeted therapy owing to their unique advantages, such as their nano nature, double lipid membrane, ability to serve as multiple carriers, good histocompatibility, high bioavailability, low cytotoxicity and immunogenicity, long life span, and high cargo capacity [97,98,99]. Exosomes can further target tumor cells through surface receptors, reducing side effects on healthy tissue. The stability of circRNAs and their function as miRNA molecular sponges suggest that circRNAs could be used as drug therapy targets. A variety of circRNAs have been proved to promote cancer progression. Moreover, whereas drugs such as specific small interfering RNAs (siRNAs) targeting specific circRNAs are inherently unstable and easily degraded, their encapsulation in exosomes can maintain the stability of siRNAs and reduce the expression of circRNAs in cancer cells. Exosomal circRNAs can also promote the expression of tumor suppressor genes through sponge-like uptake of miRNAs and indirectly inhibit the damage caused by circRNAs. These facts provide potential new approaches to tumor therapy using exosomal circRNAs. Tumor suppressor circRNAs are downregulated in tumors, and overexpression of circRNAs in tumor cells through exosomes may inhibit tumor progression; cancer-promoting circRNAs are upregulated in tumors, and siRNAs targeting circRNAs delivered by exosomes may downregulate the expression of cancer-promoting circRNAs and thus inhibit tumor progression. Given the important biological functions of exosomal circRNAs in tumor chemoresistance, the therapeutic use of RNAs targeting exosomal circRNAs has the potential to reverse tumor chemoresistance. Exosomal circRNAs have promising clinical applications as targets for tumor therapy. However, circRNAs are still in the research stage, and the clinical applications of exosomal circRNAs require deeper exploration.
Upregulation of circ_0000199 in circulating exosomes of OSCC patients is positively correlated with poor survival; thus, circulating exosomal circ_0000199 could be used as a diagnostic biomarker and potential therapeutic target in OSCC patients . By combining the in vitro and in vivo studies, exosomal circGDI2 can regulate the malignant behavior of OSCC cells by targeting the miR-424-5p/SCAI axis and is expected to serve as an exosome-based biomarker and therapeutic target for OSCC . The circulating exosomes were obtained from 210 patients with nasopharyngeal carcinoma (NPC); the result suggested that circMYC is an oncogene in NPC cells that enhances the resistance of NPC cells to radiotherapy; circMYC in circulating exosomes could be a potential therapeutic target for NPC . CircFNDC3B has been shown to regulate progression of papillary thyroid cancer (PTC) progression in tissues and cell lines through the miR-1178/TLR4 pathway ; it may thus be an effective therapeutic target for the treatment of PTC.
A series of in vitro and in vivo assays were applied to elucidate that circLONP2 acts as a key metastasis initiator in CRC progression by regulating intracellular maturation and intercellular transfer of miR-17, promoting the ability to initiate metastasis at the primary site and the formation of metastatic foci in other tissues. Therefore, it could serve as an effective prognostic predictor and as a new target for anti-metastatic therapy in CRC treatment . Transfecting specific siRNAs in CRC cells was shown to inhibit the expression of circRNA-ACAP2 and circCCDC66 and significantly reduced cell proliferation, invasion, and metastasis in the treatment group compared with the control group [87, 88]. Exosomal circ_IFT80 promotes tumorigenesis and reduces radiosensitivity by regulating the miR-296-5p/MSI1 axis in vitro and in vivo, potentially indicating a new strategy for the treatment of CRC .
Bone marrow mesenchymal stem cell (BM-MSCs) exosomal circ_0030167 promotes progression and acquisition of stem cell properties in PC cell lines through the miR-338-5p/wif1/Wnt 8/β-catenin axis, offering new prospects for PC treatment . Ye et al.  showed that hsa_circ_0000069 gene downregulation could inhibit the development of pancreatic carcinogenesis and the malignant transformation of HPDE cells, indicating that it may be an effective therapeutic target for PC therapy. The interplay network of hsa_circ_0002130–hsa_miR_4482-3p–NBN suggests the possible existence of sponge-attracting miRNAs and target mRNAs, and indicates a role for circRNAs in exploring the molecular mechanisms of PC cell reaggregation after radiotherapy, as well as their potential function as therapeutic targets .
Exosomal circ_0061395 promotes the growth of HCC cells by competitively binding to miR-877-5p and increasing the expression of PIK3R3, and could therefore be an effective target for HCC therapy . Exosomal circUHRF1, which is mainly secreted by HCC cells, can promote immunosuppression by inducing natural killer cell dysfunction, which may lead to resistance to anti-PD1 immunotherapy and provides a potential therapeutic strategy for HCC patients . Data have shown that circRNAs are abundant and stable in exosomes and are not only novel participants in the pathogenesis of cholangiocarcinoma but also good noninvasive diagnostic biomarkers in vitro and in vivo .
In renal cell carcinoma, circ_400068 has an important regulatory role, and the circ_400068/miR-210-5p/SOCS1 axis may be a candidate therapeutic target for renal cell carcinoma treatment in vitro and in vivo . Li et al.  showed that circPRRC2A can competitively bind miR-514a-5p and miR-6776-5p and reduce the degradation of the tissue-specific oncogene TRPM3, which in turn promotes tumor growth and invasion. High expression of circPRRC2A is positively correlated with clinical stage and decreased survival in patients with advanced renal cell carcinoma and is expected to become a therapeutic target for renal cell carcinoma. Tumor-derived exosomal circPSMA1 promotes development, invasion, and metastasis of triple-negative breast cancer (TNBC) via the miR-637/Akt1/β-catenin (cyclin D1) axis, providing a new perspective from which to explore new potential biomarkers and immunotherapeutic strategies for TNBC in vitro and in vivo . CircHIF1A from the exosomes of hypoxic cancer-associated fibroblasts (CAFs) has an important role in maintaining the stem cell properties of breast cancer cells, and circHIF1A may serve as an effective target molecule for breast cancer therapy .
Han et al.  showed that exosomal circRNA_0001445 promotes glioma progression through the miRNA-127-5p/SNX5 signaling pathway in vitro, providing new insights that could be used to explore the molecular mechanisms of this process. CircRNA_0001445 is thus a promising therapeutic target for glioma. CircSMARCA5 acts as a potent pharmacological tumor suppressor in glioblastoma and functions by bundling RBP SRSF1 in vitro and in vivo . Li et al.  found that the transfer of circ-0000190 encapsulated by extracellular vehicles (EVs) from normal cells to OS cells could reduce the proliferation, invasion, and migration ability of OS cells, suggesting that EVs encapsulating circ-0000190 could be constructed and used to affect intercellular communication between normal cells and OS cells, thereby inhibiting the progression of OS.
Regulatory factors and mechanisms of exosomal circRNAs
The clarification of biological functions forms a basis for probing ideal tumor markers, and identifying the regulatory factors of exosomal circRNAs and the mechanisms by which they affect malignant tumor cell growth is the basis for deciding whether exosomal circRNAs can become novel diagnostic markers and therapeutic targets for malignant tumors. The causes and mechanisms of tumor growth are very complex and include regulation of tumor cells apoptosis and proliferation, invasion and metastasis, and modulation of tumor chemotherapy resistance and radiosensitivity.
Regulatory factors of exosomal circRNAs
Several recent studies have shown that multiple regulatory factors can modulate the expression of exosomal circRNAs in malignancies, e.g., sevoflurane, arsenite, hypoxia, and matrine. Sevoflurane inhibits CRC progression by modulating the circ-HMGCS1/miR-34a-5p/SGPP1 axis when delivered by exosomes . Hypoxia-derived exosomal circ-133 is transferred into normoxic CRC cells and promotes CRC cell migration through the miR-133a/GEF-H1/RhoA axis; this finding reveals a potential mechanism by which intra-tumor oxygen heterogeneity promotes tumor progression . Gu et al.  showed that matrine inhibited the occurrence of CRC by blocking the release of exosomal circSLC7A6 from CAFs, providing a strong rationale for the use of matrine in the treatment of CRC.
Dai et al.  showed that long-term exposure to arsenite could induce malignant transformation and overexpression of circRNA_100284 in L-02 cells, and that circRNA_100284 could be transported from transformed L-02 cells to normal cells via exosomes. In normal cells, exosomal circRNA_100284 induced cell cycle acceleration and promoted proliferation by interacting with miR217, suggesting that arsenite exerts its oncogenic effects via a mechanism involving induction of circRNAs.
Possible mechanism of exosome circRNAs
CircRNAs have been confirmed to exist in exosomes, suggesting a new direction for the study of circRNAs. CircRNAs are mostly located in the cytoplasm, and the types of circRNAs in exosomes vary according to the type of cytoplasm, suggesting that the transfer of specific circRNAs to exosomes may be a positively regulated and selective process. Exosomal circRNAs can regulate tumor growth by regulating tumor cells apoptosis and proliferation, invasion and metastasis, and modulating tumor chemotherapy resistance and radiosensitivity. Exosomal circRNAs can target multiple oncogenes or proteins, e.g., miRNA-302b-3p/IGF-1R, miR-424-5p/SCAI, miR-1178/TLR4, and Wnt/β-catenin, to promote their expression and enable them to exert their growth-promoting effects. The target molecules of exosomal circRNAs in a variety of malignancies are shown in Table 2, Figs. 1 and 2.
Exosomal circRNAs that can regulate tumor cell proliferation, invasion, metastasis, and drug resistance represent a new hotspot in tumor research. CircRNAs have highly conserved characteristics and tissue-specific expression patterns; they can be enriched in exosomes and are easily detected in various body fluids. Therefore, exploring the association between exosomes and circRNAs will not only have a profound impact on our understanding of the functions and characteristics of exosomes but it will also provide new strategies to inhibit tumor progression and reverse drug resistance, as well helping to identify new potential tumor biomarkers and therapeutic targets. At present, only a few circRNAs have defined functions or clinical applications, and our understanding of exosomal circRNAs is still very limited; a large number of exosomal circRNAs and their mechanisms of actions have not been identified. The diagnostic value of exosomal circRNAs in different tumors still lacks experimental verification. The advantages of exosomal circRNAs over circulating free circRNAs has also not been fully validated. Therefore, exosomal circRNAs are expected to be a focus of future research, and their clinical application value needs to be supported by sufficient theoretical results.
Availability of data and materials
Competing endogenous RNAs
Long non-coding RNA
Heat shock protein
Human umbilical vein endothelial cells
Mitogenactivated protein kinase 1
Area under curve
Early gastric cancer
FLI1 exonic circular RNAs 1
Programmed cell death ligand 1
Bonemarrow mesenchymal stem cells
Laryngeal squamous cell carcinoma
Oral squamous cell carcinoma
Papillary thyroid carcinoma
Esophageal squamous cell carcinoma
Pancreatic ductal adenocarcinoma
Triple-negative breast cancer
Non-small cell lung cancer
Small-cell lung cancer
Urothelial carcinoma of the bladder
Renal cell carcinoma
Cutaneous squamous cell carcinoma
Acute myeloid leukemia
Braicu C, Tomuleasa C, Monroig P, Cucuianu A, Berindan-Neagoe I, Calin GA. Exosomes as divine messengers: are they the Hermes of modern molecular oncology? Cell Death Differ. 2015;22(1):34–45. https://doi.org/10.1038/cdd.2014.130.
Meng X, Li X, Zhang P, Wang J, Zhou Y, Chen M. Circular RNA: an emerging key player in RNA world. Brief Bioinform. 2017;18(4):547–57. https://doi.org/10.1093/bib/bbw045.
Li Y, Zheng Q, Bao C, Li S, Guo W, Zhao J, et al. Circular RNA is enriched and stable in exosomes: a promising biomarker for cancer diagnosis. Cell Res. 2015;25(8):981–4. https://doi.org/10.1038/cr.2015.82.
Shang Q, Yang Z, Jia R, Ge S. The novel roles of circRNAs in human cancer. Mol Cancer. 2019;18(1):6. https://doi.org/10.1186/s12943-018-0934-6.
Xu R, Rai A, Chen M, Suwakulsiri W, Greening DW, Simpson RJ. Extracellular vesicles in cancer—implications for future improvements in cancer care. Nat Rev Clin Oncol. 2018;15(10):617–38. https://doi.org/10.1038/s41571-018-0036-9.
Kalluri R, LeBleu VS. The biology, function, and biomedical applications of exosomes. Science. 2020. https://doi.org/10.1126/science.aau6977.
Yang D, Zhang W, Zhang H, Zhang F, Chen L, Ma L, et al. Progress, opportunity, and perspective on exosome isolation—efforts for efficient exosome-based theranostics. Theranostics. 2020;10(8):3684–707. https://doi.org/10.7150/thno.41580.
Mohammadi S, Yousefi F, Shabaninejad Z, Movahedpour A, Mahjoubin Tehran M, Shafiee A, et al. Exosomes and cancer: from oncogenic roles to therapeutic applications. IUBMB Life. 2020;72(4):724–48. https://doi.org/10.1002/iub.2182.
Gu M, Li L, Zhang Z, Chen J, Zhang W, Zhang J, et al. PFKFB3 promotes proliferation, migration and angiogenesis in nasopharyngeal carcinoma. J Cancer. 2017;8(18):3887–96. https://doi.org/10.7150/jca.19112.
Milane L, Singh A, Mattheolabakis G, Suresh M, Amiji MM. Exosome mediated communication within the tumor microenvironment. J Control Release. 2015;219:278–94. https://doi.org/10.1016/j.jconrel.2015.06.029.
Shi H, Li H, Zhen T, Dong Y, Pei X, Zhang X. The potential therapeutic role of exosomal microRNA-520b derived from normal fibroblasts in pancreatic cancer. Mol Ther Nucleic Acids. 2020;20:373–84. https://doi.org/10.1016/j.omtn.2019.12.029.
Kim DH, Park S, Kim H, Choi YJ, Kim SY, Sung KJ, et al. Tumor-derived exosomal miR-619–5p promotes tumor angiogenesis and metastasis through the inhibition of RCAN1.4. Cancer Lett. 2020;475:2–13. https://doi.org/10.1016/j.canlet.2020.01.023.
Li X, Wang X. The emerging roles and therapeutic potential of exosomes in epithelial ovarian cancer. Mol Cancer. 2017;16(1):92. https://doi.org/10.1186/s12943-017-0659-y.
You Y, Shan Y, Chen J, Yue H, You B, Shi S, et al. Matrix metalloproteinase 13-containing exosomes promote nasopharyngeal carcinoma metastasis. Cancer Sci. 2015;106(12):1669–77. https://doi.org/10.1111/cas.12818.
Chan YK, Zhang H, Liu P, Yue H, You B, Shi S, et al. Proteomic analysis of exosomes from nasopharyngeal carcinoma cell identifies intercellular transfer of angiogenic proteins. Int J Cancer. 2015;137(8):1830–41. https://doi.org/10.1002/ijc.29562.
Lu J, Liu QH, Wang F, Tan JJ, Deng YQ, Peng XH, et al. Exosomal miR-9 inhibits angiogenesis by targeting MDK and regulating PDK/AKT pathway in nasopharyngeal carcinoma. J Exp Clin Cancer Res. 2018;37(1):147. https://doi.org/10.1186/s13046-018-0814-3.
Isola AL, Eddy K, Zembrzuski K, Goydos JS, Chen S. Exosomes released by metabotropic glutamate receptor 1 (GRM1) expressing melanoma cells increase cell migration and invasiveness. Oncotarget. 2018;9(1):1187–99. https://doi.org/10.18632/oncotarget.23455.
Hou J, Wang F, Liu X, Song M, Yin X. Tumor-derived exosomes enhance invasion and metastasis of salivary adenoid cystic carcinoma cells. J Oral Pathol Med. 2018;47(2):144–51. https://doi.org/10.1111/jop.12654.
Barros FM, Carneiro F, Machado JC, Melo SA. Exosomes and immune response in cancer: friends or foes? Front Immunol. 2018;9:730. https://doi.org/10.3389/fimmu.2018.00730.
Jeck WR, Sorrentino JA, Wang K, Slevin MK, Burd CE, Liu J, et al. Circular RNAs are abundant, conserved, and associated with ALU repeats. RNA. 2013;19(2):141–57. https://doi.org/10.1261/rna.035667.112.
Su M, Xiao Y, Ma J, Tang Y, Tian B, Zhang Y, et al. Circular RNAs in cancer: emerging functions in hallmarks, stemness, resistance and roles as potential biomarkers. Mol Cancer. 2019;18(1):90. https://doi.org/10.1186/s12943-019-1002-6.
Wang Y, Liu J, Ma J, Sun T, Zhou Q, Wang W, et al. Exosomal circRNAs: biogenesis, effect and application in human diseases. Mol Cancer. 2019;18(1):116. https://doi.org/10.1186/s12943-019-1041-z.
Tian L, Cao J, Jiao H, Zhang J, Ren X, Liu X, et al. CircRASSF2 promotes laryngeal squamous cell carcinoma progression by regulating the miR-302b-3p/IGF-1R axis. Clin Sci. 2019;133(9):1053–66. https://doi.org/10.1042/cs20190110.
Dai X, Chen C, Yang Q, Xue J, Chen X, Sun B, et al. Exosomal circRNA_100284 from arsenite-transformed cells, via microRNA-217 regulation of EZH2, is involved in the malignant transformation of human hepatic cells by accelerating the cell cycle and promoting cell proliferation. Cell Death Dis. 2018;9(5):454. https://doi.org/10.1038/s41419-018-0485-1.
Zhang H, Deng T, Ge S, Liu Y, Bai M, Zhu K, et al. Exosome circRNA secreted from adipocytes promotes the growth of hepatocellular carcinoma by targeting deubiquitination-related USP7. Oncogene. 2019;38(15):2844–59. https://doi.org/10.1038/s41388-018-0619-z.
Feng W, Gong H, Wang Y, Zhu G, Xue T, Wang Y, et al. circIFT80 functions as a ceRNA of miR-1236-3p to promote colorectal cancer progression. Mol Ther Nucleic Acids. 2019;18:375–87. https://doi.org/10.1016/j.omtn.2019.08.024.
Li Y, Li C, Xu R, Wang Y, Li D, Zhang B. A novel circFMN2 promotes tumor proliferation in CRC by regulating the miR-1182/hTERT signaling pathways. Clin Sci. 2019;133(24):2463–79. https://doi.org/10.1042/cs20190715.
Yu L, Xie J, Liu X, Yu Y, Wang S. Plasma exosomal circNEK9 accelerates the progression of gastric cancer via miR-409–3p/MAP7 axis. Dig Dis Sci. 2021. https://doi.org/10.1007/s10620-020-06816-z.
Zhang X, Wang S, Wang H, Cao J, Huang X, Chen Z, et al. Circular RNA circNRIP1 acts as a microRNA-149-5p sponge to promote gastric cancer progression via the AKT1/mTOR pathway. Mol Cancer. 2019;18(1):20. https://doi.org/10.1186/s12943-018-0935-5.
Wang D, Ming X, Xu J, Xiao Y. Circ_0009910 shuttled by exosomes regulates proliferation, cell cycle and apoptosis of acute myeloid leukemia cells by regulating miR-5195-3p/GRB10 axis. Hematol Oncol. 2021;39(3):390–400. https://doi.org/10.1002/hon.2874.
Li T, Sun X, Chen L. Exosome circ_0044516 promotes prostate cancer cell proliferation and metastasis as a potential biomarker. J Cell Biochem. 2020;121(3):2118–26. https://doi.org/10.1002/jcb.28239.
Ma R, Ye X, Cheng H, Cui H, Chang X. Tumor-derived exosomal circRNA051239 promotes proliferation and migration of epithelial ovarian cancer. Am J Transl Res. 2021;13(3):1125–39.
Qin W, Tsukasaki Y, Dasgupta S, Mukhopadhyay N, Ikebe M, Sauter ER. Exosomes in human breast milk promote EMT. Clin Cancer Res. 2016;22(17):4517–24. https://doi.org/10.1158/1078-0432.Ccr-16-0135.
Huang XY, Huang ZL, Huang J, Xu B, Huang XY, Xu YH, et al. Exosomal circRNA-100338 promotes hepatocellular carcinoma metastasis via enhancing invasiveness and angiogenesis. J Exp Clin Cancer Res. 2020;39(1):20. https://doi.org/10.1186/s13046-020-1529-9.
Wang G, Liu W, Zou Y, Wang G, Deng Y, Luo J, et al. Three isoforms of exosomal circPTGR1 promote hepatocellular carcinoma metastasis via the miR449a-MET pathway. EBioMedicine. 2019;40:432–45. https://doi.org/10.1016/j.ebiom.2018.12.062.
Zhu C, Su Y, Liu L, Wang S, Liu Y, Wu J. Circular RNA hsa_circ_0004277 stimulates malignant phenotype of hepatocellular carcinoma and epithelial-mesenchymal transition of peripheral cells. Front Cell Dev Biol. 2020;8: 585565. https://doi.org/10.3389/fcell.2020.585565.
Wang S, Hu Y, Lv X, Li B, Gu D, Li Y, et al. Circ-0000284 arouses malignant phenotype of cholangiocarcinoma cells and regulates the biological functions of peripheral cells through cellular communication. Clin Sci. 2019;133(18):1935–53. https://doi.org/10.1042/cs20190589.
Li J, Li Z, Jiang P, Peng M, Zhang X, Chen K, et al. Circular RNA IARS (circ-IARS) secreted by pancreatic cancer cells and located within exosomes regulates endothelial monolayer permeability to promote tumor metastasis. J Exp Clin Cancer Res. 2018;37(1):177. https://doi.org/10.1186/s13046-018-0822-3.
Li Z, Yanfang W, Li J, Jiang P, Peng T, Chen K, et al. Tumor-released exosomal circular RNA PDE8A promotes invasive growth via the miR-338/MACC1/MET pathway in pancreatic cancer. Cancer Lett. 2018;432:237–50. https://doi.org/10.1016/j.canlet.2018.04.035.
Lu J, Wang YH, Yoon C, Huang XY, Xu Y, Xie JW, et al. Circular RNA circ-RanGAP1 regulates VEGFA expression by targeting miR-877-3p to facilitate gastric cancer invasion and metastasis. Cancer Lett. 2020;471:38–48. https://doi.org/10.1016/j.canlet.2019.11.038.
Chen X, Chen RX, Wei WS, Huang XY, Xu Y, Xie JW, et al. PRMT5 circular RNA promotes metastasis of urothelial carcinoma of the bladder through sponging miR-30c to induce epithelial-mesenchymal transition. Clin Cancer Res. 2018;24(24):6319–30. https://doi.org/10.1158/1078-0432.Ccr-18-1270.
Li L, Li W, Chen N, Zhao H, Xu G, Zhao Y, et al. FLI1 exonic circular RNAs as a novel oncogenic driver to promote tumor metastasis in small cell lung cancer. Clin Cancer Res. 2019;25(4):1302–17. https://doi.org/10.1158/1078-0432.Ccr-18-1447.
Guan X, Zong ZH, Liu Y, Chen S, Wang LL, Zhao Y. circPUM1 promotes tumorigenesis and progression of ovarian cancer by sponging miR-615-5p and miR-6753-5p. Mol Ther Nucleic Acids. 2019;18:882–92. https://doi.org/10.1016/j.omtn.2019.09.032.
Zong ZH, Du YP, Guan X, Chen S, Zhao Y. CircWHSC1 promotes ovarian cancer progression by regulating MUC1 and hTERT through sponging miR-145 and miR-1182. J Exp Clin Cancer Res. 2019;38(1):437. https://doi.org/10.1186/s13046-019-1437-z.
Zhao H, Chen S, Fu Q. Exosomes from CD133(+) cells carrying circ-ABCC1 mediate cell stemness and metastasis in colorectal cancer. J Cell Biochem. 2020;121(5–6):3286–97. https://doi.org/10.1002/jcb.29600.
Gao D, Zhang X, Liu B, Meng D, Fang K, Guo Z, et al. Screening circular RNA related to chemotherapeutic resistance in breast cancer. Epigenomics. 2017;9(9):1175–88. https://doi.org/10.2217/epi-2017-0055.
Wang P, Sun Y, Yang Y, Chen Y, Liu H. Circ_0067835 knockdown enhances the radiosensitivity of colorectal cancer by miR-296-5p/IGF1R axis. Onco Targets Ther. 2021;14:491–502. https://doi.org/10.2147/ott.S281011.
Zheng P, Chen L, Yuan X, Meng D, Fang K, Guo Z, et al. Exosomal transfer of tumor-associated macrophage-derived miR-21 confers cisplatin resistance in gastric cancer cells. J Exp Clin Cancer Res. 2017;36(1):53. https://doi.org/10.1186/s13046-017-0528-y.
Zhong Y, Wang D, Ding Y, Tian G, Jiang B. Circular RNA circ_0032821 contributes to oxaliplatin (OXA) resistance of gastric cancer cells by regulating SOX9 via miR-515-5p. Biotech Lett. 2021;43(2):339–51. https://doi.org/10.1007/s10529-020-03036-3.
Hon KW, Ab-Mutalib NS, Abdullah NMA, Jamal R, Abu N. Extracellular vesicle-derived circular RNAs confers chemoresistance in colorectal cancer. Sci Rep. 2019;9(1):16497. https://doi.org/10.1038/s41598-019-53063-y.
Wang X, Zhang H, Yang H, Bai M, Ning T, Deng T, et al. Exosome-delivered circRNA promotes glycolysis to induce chemoresistance through the miR-122-PKM2 axis in colorectal cancer. Mol Oncol. 2020;14(3):539–55. https://doi.org/10.1002/1878-0261.12629.
Zeng Z, Zhao Y, Chen Q, Zhu S, Niu Y, Ye Z, et al. Hypoxic exosomal HIF-1α-stabilizing circZNF91 promotes chemoresistance of normoxic pancreatic cancer cells via enhancing glycolysis. Oncogene. 2021. https://doi.org/10.1038/s41388-021-01960-w.
Xu X, Tao R, Sun L, Ji X. Exosome-transferred hsa_circ_0014235 promotes DDP chemoresistance and deteriorates the development of non-small cell lung cancer by mediating the miR-520a-5p/CDK4 pathway. Cancer Cell Int. 2020;20(1):552. https://doi.org/10.1186/s12935-020-01642-9.
Ma J, Qi G, Li L. A novel serum exosomes-based biomarker hsa_circ_0002130 facilitates osimertinib-resistance in non-small cell lung cancer by sponging miR-498. Onco Targets Ther. 2020;13:5293–307. https://doi.org/10.2147/ott.S243214.
Hu K, Liu X, Li Y, Li Q, Xu Y, Zeng W, et al. exosomes mediated transfer of Circ_UBE2D2 enhances the resistance of breast cancer to tamoxifen by binding to miR-200a-3p. Med Sci Monit. 2020;26:e922253. https://doi.org/10.12659/msm.922253.
Zhao Z, Ji M, Wang Q, He N, Li Y. Circular RNA Cdr1as upregulates SCAI to suppress cisplatin resistance in ovarian cancer via miR-1270 suppression. Mol Ther Nucleic Acids. 2019;18:24–33. https://doi.org/10.1016/j.omtn.2019.07.012.
Pan Y, Lin Y, Mi C. Cisplatin-resistant osteosarcoma cell-derived exosomes confer cisplatin resistance to recipient cells in an exosomal circ_103801-dependent manner. Cell Biol Int. 2021;45(4):858–68. https://doi.org/10.1002/cbin.11532.
Siravegna G, Marsoni S, Siena S, Bardelli A. Integrating liquid biopsies into the management of cancer. Nat Rev Clin Oncol. 2017;14(9):531–48. https://doi.org/10.1038/nrclinonc.2017.14.
Li S, Li Y, Chen B, Zhao J, Yu S, Tang Y, et al. exoRBase: a database of circRNA, lncRNA and mRNA in human blood exosomes. Nucleic Acids Res. 2018;46(D1):D106-d112. https://doi.org/10.1093/nar/gkx891.
Morton DJ, Kuiper EG, Jones SK, Leung SW, Corbett AH, Fasken MB. The RNA exosome and RNA exosome-linked disease. RNA. 2018;24(2):127–42. https://doi.org/10.1261/rna.064626.117.
Xu Z, Yan Y, Zeng S, Dai S, Chen X, Wei J, et al. Circular RNAs: clinical relevance in cancer. Oncotarget. 2018;9(1):1444–60. https://doi.org/10.18632/oncotarget.22846.
Han J, Lin Q, Dong C. Plasma cell-free circRNAs panel act as fingerprint predicts the occurrence of laryngeal squamous cell carcinoma. Aging. 2021;13(13):17328–36. https://doi.org/10.18632/aging.203215.
Liu S, Lin Z, Rao W, Zheng J, Xie Q, Lin Y, et al. Upregulated expression of serum exosomal hsa_circ_0026611 is associated with lymph node metastasis and poor prognosis of esophageal squamous cell carcinoma. J Cancer. 2021;12(3):918–26. https://doi.org/10.7150/jca.50548.
Lu Q, Wang X, Zhu J, Fei X, Chen H, Li C. Hypoxic tumor-derived exosomal Circ0048117 facilitates M2 macrophage polarization acting as miR-140 sponge in esophageal squamous cell carcinoma. Onco Targets Ther. 2020;13:11883–97. https://doi.org/10.2147/ott.S284192.
Fan L, Cao Q, Liu J, Zhang J, Li B. Circular RNA profiling and its potential for esophageal squamous cell cancer diagnosis and prognosis. Mol Cancer. 2019;18(1):16. https://doi.org/10.1186/s12943-018-0936-4.
Dou Y, Cha DJ, Franklin JL, Higginbotham JN, Jeppesen DK, Weaver AM, et al. Circular RNAs are down-regulated in KRAS mutant colon cancer cells and can be transferred to exosomes. Sci Rep. 2016;6:37982. https://doi.org/10.1038/srep37982.
Pan B, Qin J, Liu X, He B, Wang X, Pan Y, et al. Identification of serum exosomal hsa-circ-0004771 as a novel diagnostic biomarker of colorectal cancer. Front Genet. 2019;10:1096. https://doi.org/10.3389/fgene.2019.01096.
Barbagallo C, Brex D, Caponnetto A, Cirnigliaro M, Scalia M, Magnano A, et al. LncRNA UCA1, upregulated in CRC biopsies and downregulated in serum exosomes, controls mRNA expression by RNA-RNA interactions. Mol Ther Nucleic Acids. 2018;12:229–41. https://doi.org/10.1016/j.omtn.2018.05.009.
Xie M, Yu T, Jing X, Ma L, Fan Y, Yang F, et al. Exosomal circSHKBP1 promotes gastric cancer progression via regulating the miR-582–3p/HUR/VEGF axis and suppressing HSP90 degradation. Mol Cancer. 2020;19(1):112. https://doi.org/10.1186/s12943-020-01208-3.
Shao Y, Tao X, Lu R, Zhang H, Ge J, Xiao B, et al. Hsa_circ_0065149 is an indicator for early gastric cancer screening and prognosis prediction. Pathol Oncol Res. 2020;26(3):1475–82. https://doi.org/10.1007/s12253-019-00716-y.
Sun XH, Wang YT, Li GF, Zhang N, Fan L. Serum-derived three-circRNA signature as a diagnostic biomarker for hepatocellular carcinoma. Cancer Cell Int. 2020;20:226. https://doi.org/10.1186/s12935-020-01302-y.
Chen W, Quan Y, Fan S, Wang H, Liang J, Huang L, et al. Exosome-transmitted circular RNA hsa_circ_0051443 suppresses hepatocellular carcinoma progression. Cancer Lett. 2020;475:119–28. https://doi.org/10.1016/j.canlet.2020.01.022.
Yang B, Teng F, Chang L, Wang J, Liu DL, Cui YS, et al. Tumor-derived exosomal circRNA_102481 contributes to EGFR-TKIs resistance via the miR-30a-5p/ROR1 axis in non-small cell lung cancer. Aging. 2021;13(9):13264–86. https://doi.org/10.18632/aging.203011.
Chen T, Liu Y, Li C, Ding C, Chen J, Zhao J. Tumor-derived exosomal circFARSA mediates M2 macrophage polarization via the PTEN/PI3K/AKT pathway to promote non-small cell lung cancer metastasis. Cancer Treat Res Commun. 2021;28:100412. https://doi.org/10.1016/j.ctarc.2021.100412.
Wang J, Zhao X, Wang Y, Ren F, Sun D, Yan Y, et al. circRNA-002178 act as a ceRNA to promote PDL1/PD1 expression in lung adenocarcinoma. Cell Death Dis. 2020;11(1):32. https://doi.org/10.1038/s41419-020-2230-9.
Chen F, Huang C, Wu Q, Jiang L, Chen S, Chen L. Circular RNAs expression profiles in plasma exosomes from early-stage lung adenocarcinoma and the potential biomarkers. J Cell Biochem. 2020;121(3):2525–33. https://doi.org/10.1002/jcb.29475.
Lin S, Xiong W, Liu H, Pei L, Yi H, Guan Y. Profiling and integrated analysis of differentially expressed circular RNAs in plasma exosomes as novel biomarkers for advanced-stage lung adenocarcinoma. Onco Targets Ther. 2020;13:12965–77. https://doi.org/10.2147/ott.S279710.
Xu L, Liao WL, Lu QJ, Zhang P, Zhu J, Jiang GN. Hypoxic tumor-derived exosomal circular RNA SETDB1 promotes invasive growth and EMT via the miR-7/Sp1 axis in lung adenocarcinoma. Mol Ther Nucleic Acids. 2021;23:1078–92. https://doi.org/10.1016/j.omtn.2021.01.019.
Yang SJ, Wang DD, Zhou SY, Zhang Q, Wang JY, Zhong SL, et al. Identification of circRNA-miRNA networks for exploring an underlying prognosis strategy for breast cancer. Epigenomics. 2020;12(2):101–25. https://doi.org/10.2217/epi-2019-0058.
Wang J, Zhang Q, Zhou S, Xu H, Wang D, Feng J, et al. Circular RNA expression in exosomes derived from breast cancer cells and patients. Epigenomics. 2019;11(4):411–21. https://doi.org/10.2217/epi-2018-0111.
Wang X, Yao Y, Jin M. Circ-0001068 is a novel biomarker for ovarian cancer and inducer of PD1 expression in T cells. Aging. 2020;12(19):19095–106. https://doi.org/10.18632/aging.103706.
Zhang Z, Guo H, Yang W, Li J. Exosomal circular RNA RNA-seq profiling and the carcinogenic role of exosomal circ-CYP24A1 in cutaneous squamous cell carcinoma. Front Med. 2021;8: 675842. https://doi.org/10.3389/fmed.2021.675842.
Luo Y, Gui R. Circulating exosomal circMYC is associated with recurrence and bortezomib resistance in patients with multiple myeloma. Turk J Haematol. 2020;37(4):248–62. https://doi.org/10.4274/tjh.galenos.2020.2020.0243.
Ding C, Yi X, Wu X, Bu X, Wang D, Wu Z, et al. Exosome-mediated transfer of circRNA CircNFIX enhances temozolomide resistance in glioma. Cancer Lett. 2020;479:1–12. https://doi.org/10.1016/j.canlet.2020.03.002.
Han C, Wang S, Wang H, Zhang J. Exosomal circ-HIPK3 facilitates tumor progression and temozolomide resistance by regulating miR-421/ZIC5 axis in glioma. Cancer Biother Radiopharm. 2020. https://doi.org/10.1089/cbr.2019.3492.
Chen L, Zhang S, Wu J, Cui J, Zhong L, Zeng L, et al. circRNA_100290 plays a role in oral cancer by functioning as a sponge of the miR-29 family. Oncogene. 2017;36(32):4551–61. https://doi.org/10.1038/onc.2017.89.
Hsiao KY, Lin YC, Gupta SK, Chang N, Yen L, Sun HS, et al. Noncoding effects of circular RNA CCDC66 promote colon cancer growth and metastasis. Can Res. 2017;77(9):2339–50. https://doi.org/10.1158/0008-5472.Can-16-1883.
He JH, Li YG, Han ZP, Zhou JB, Chen WM, Lv YB, et al. The circRNA-ACAP2/Hsa-miR-21-5p/Tiam1 regulatory feedback circuit affects the proliferation, migration, and invasion of colon cancer SW480 cells. Cell Physiol Biochem. 2018;49(4):1539–50. https://doi.org/10.1159/000493457.
Zhou LH, Yang YC, Zhang RY, Wang P, Pang MH, Liang LQ. CircRNA_0023642 promotes migration and invasion of gastric cancer cells by regulating EMT. Eur Rev Med Pharmacol Sci. 2018;22(8):2297–303. https://doi.org/10.26355/eurrev_201804_14818.
Zhu P, Ge N, Liu D, Yang F, Zhang K, Guo J, et al. Preliminary investigation of the function of hsa_circ_0006215 in pancreatic cancer. Oncol Lett. 2018;16(1):603–11. https://doi.org/10.3892/ol.2018.8652.
Ma HB, Yao YN, Yu JJ, Chen XX, Li HF. Extensive profiling of circular RNAs and the potential regulatory role of circRNA-000284 in cell proliferation and invasion of cervical cancer via sponging miR-506. Am J Transl Res. 2018;10(2):592–604.
Liu J, Wang D, Long Z, Liu J, Li W. CircRNA8924 promotes cervical cancer cell proliferation, migration and invasion by competitively binding to miR-518d-5p /519-5p family and modulating the expression of CBX8. Cell Physiol Biochem. 2018;48(1):173–84. https://doi.org/10.1159/000491716.
Kai D, Yannian L, Yitian C, Dinghao G, Xin Z, Wu J. Circular RNA HIPK3 promotes gallbladder cancer cell growth by sponging microRNA-124. Biochem Biophys Res Commun. 2018;503(2):863–9. https://doi.org/10.1016/j.bbrc.2018.06.088.
Liu Y, Lu C, Zhou Y, Zhang Z, Sun L. Circular RNA hsa_circ_0008039 promotes breast cancer cell proliferation and migration by regulating miR-432-5p/E2F3 axis. Biochem Biophys Res Commun. 2018;502(3):358–63. https://doi.org/10.1016/j.bbrc.2018.05.166.
Kun-Peng Z, Xiao-Long M, Chun-Lin Z. Overexpressed circPVT1, a potential new circular RNA biomarker, contributes to doxorubicin and cisplatin resistance of osteosarcoma cells by regulating ABCB1. Int J Biol Sci. 2018;14(3):321–30. https://doi.org/10.7150/ijbs.24360.
Liu X, Zhong Y, Li J, Shan A. Circular RNA circ-NT5C2 acts as an oncogene in osteosarcoma proliferation and metastasis through targeting miR-448. Oncotarget. 2017;8(70):114829–38. https://doi.org/10.18632/oncotarget.22162.
Fan Q, Yang L, Zhang X, Peng X, Wei S, Su D, et al. The emerging role of exosome-derived non-coding RNAs in cancer biology. Cancer Lett. 2018;414:107–15. https://doi.org/10.1016/j.canlet.2017.10.040.
Srivastava A, Filant J, Moxley KM, Sood A, McMeekin S, Ramesh R. Exosomes: a role for naturally occurring nanovesicles in cancer growth, diagnosis and treatment. Curr Gene Ther. 2015;15(2):182–92. https://doi.org/10.2174/1566523214666141224100612.
Farooqi AA, Desai NN, Qureshi MZ, Librelotto DRN, Gasparri ML, Bishayee A, et al. Exosome biogenesis, bioactivities and functions as new delivery systems of natural compounds. Biotechnol Adv. 2018;36(1):328–34. https://doi.org/10.1016/j.biotechadv.2017.12.010.
Luo Y, Liu F, Guo J, Gui R. Upregulation of circ_0000199 in circulating exosomes is associated with survival outcome in OSCC. Sci Rep. 2020;10(1):13739. https://doi.org/10.1038/s41598-020-70747-y.
Zhang Y, Tang K, Chen L, Du M, Qu Z. Exosomal CircGDI2 suppresses oral squamous cell carcinoma progression through the regulation of miR-424-5p/SCAI axis. Cancer Manag Res. 2020;12:7501–14. https://doi.org/10.2147/cmar.S255687.
Luo Y, Ma J, Liu F, Guo J, Gui R. Diagnostic value of exosomal circMYC in radioresistant nasopharyngeal carcinoma. Head Neck. 2020;42(12):3702–11. https://doi.org/10.1002/hed.26441.
Wu G, Zhou W, Pan X, Sun Z, Sun Y, Xu H, et al. Circular RNA profiling reveals exosomal circ_0006156 as a novel biomarker in papillary thyroid cancer. Mol Ther Nucleic Acids. 2020;19:1134–44. https://doi.org/10.1016/j.omtn.2019.12.025.
Han K, Wang FW, Cao CH, Ling H, Chen JW, Chen RX, et al. CircLONP2 enhances colorectal carcinoma invasion and metastasis through modulating the maturation and exosomal dissemination of microRNA-17. Mol Cancer. 2020;19(1):60. https://doi.org/10.1186/s12943-020-01184-8.
Li L, Jiang Z, Zou X, Hao T. Exosomal circ_IFT80 enhances tumorigenesis and suppresses radiosensitivity in colorectal cancer by regulating miR-296-5p/MSI1 axis. Cancer Manag Res. 2021;13:1929–41. https://doi.org/10.2147/cmar.S297123.
Yao X, Mao Y, Wu D, Zhu Y, Lu J, Huang Y, et al. Exosomal circ_0030167 derived from BM-MSCs inhibits the invasion, migration, proliferation and stemness of pancreatic cancer cells by sponging miR-338-5p and targeting the Wif1/Wnt8/β-catenin axis. Cancer Lett. 2021;512:38–50. https://doi.org/10.1016/j.canlet.2021.04.030.
Ye Z, Zhu Z, Xie J, Feng Z, Li Y, Xu X, et al. Hsa_circ_0000069 knockdown inhibits tumorigenesis and exosomes with downregulated hsa_circ_0000069 suppress malignant transformation via inhibition of STIL in pancreatic cancer. Int J Nanomed. 2020;15:9859–73. https://doi.org/10.2147/ijn.S279258.
Chen YY, Jiang MJ, Tian L. Analysis of exosomal circRNAs upon irradiation in pancreatic cancer cell repopulation. BMC Med Genom. 2020;13(1):107. https://doi.org/10.1186/s12920-020-00756-3.
Yu Y, Bian L, Liu R, Wang Y, Xiao X. Circular RNA hsa_circ_0061395 accelerates hepatocellular carcinoma progression via regulation of the miR-877–5p/PIK3R3 axis. Cancer cell Int. 2021;21(1):10. https://doi.org/10.1186/s12935-020-01695-w.
Zhang PF, Gao C, Huang XY, Lu JC, Guo XJ, Shi GM, et al. Cancer cell-derived exosomal circUHRF1 induces natural killer cell exhaustion and may cause resistance to anti-PD1 therapy in hepatocellular carcinoma. Mol Cancer. 2020;19(1):110. https://doi.org/10.1186/s12943-020-01222-5.
Louis C, Desoteux M, Coulouarn C. Exosomal circRNAs: new players in the field of cholangiocarcinoma. Clin Sci. 2019;133(21):2239–44. https://doi.org/10.1042/cs20190940.
Xiao H, Shi J. Exosomal circular RNA_400068 promotes the development of renal cell carcinoma via the miR-210-5p/SOCS1 axis. Mol Med Rep. 2020;22(6):4810–20. https://doi.org/10.3892/mmr.2020.11541.
Li W, Yang FQ, Sun CM, Huang JH, Zhang HM, Li X, et al. circPRRC2A promotes angiogenesis and metastasis through epithelial-mesenchymal transition and upregulates TRPM3 in renal cell carcinoma. Theranostics. 2020;10(10):4395–409. https://doi.org/10.7150/thno.43239.
Yang SJ, Wang DD, Zhong SL, Chen WQ, Wang FL, Zhang J, et al. Tumor-derived exosomal circPSMA1 facilitates the tumorigenesis, metastasis, and migration in triple-negative breast cancer (TNBC) through miR-637/Akt1/β-catenin (cyclin D1) axis. Cell Death Dis. 2021;12(5):420. https://doi.org/10.1038/s41419-021-03680-1.
Zhan Y, Du J, Min Z, Ma L, Zhang W, Zhu W, et al. Carcinoma-associated fibroblasts derived exosomes modulate breast cancer cell stemness through exonic circHIF1A by miR-580–5p in hypoxic stress. Cell Death Discov. 2021;7(1):141. https://doi.org/10.1038/s41420-021-00506-z.
Han Y, Liu Y, Zhang B, Yin G. Exosomal circRNA 0001445 promotes glioma progression through miRNA-127-5p/SNX5 pathway. Aging. 2021;13(9):13287–99. https://doi.org/10.18632/aging.203013.
Barbagallo D, Caponnetto A, Cirnigliaro M, Brex D, Barbagallo C, D’Angeli F, et al. CircSMARCA5 inhibits migration of glioblastoma multiforme cells by regulating a molecular axis involving splicing factors SRSF1/SRSF3/PTB. Int J Mol Sci. 2018. https://doi.org/10.3390/ijms19020480.
Li S, Pei Y, Wang W, Liu F, Zheng K, Zhang X. Extracellular nanovesicles-transmitted circular RNA has_circ_0000190 suppresses osteosarcoma progression. J Cell Mol Med. 2020;24(3):2202–14. https://doi.org/10.1111/jcmm.14877.
He J, Zhao H, Liu X, Wang D, Wang Y, Ai Y, et al. Sevoflurane suppresses cell viability and invasion and promotes cell apoptosis in colon cancer by modulating exosome-mediated circ-HMGCS1 via the miR-34a-5p/SGPP1 axis. Oncol Rep. 2020;44(6):2429–42. https://doi.org/10.3892/or.2020.7783.
Yang H, Zhang H, Yang Y, Wang X, Deng T, Liu R, et al. Hypoxia induced exosomal circRNA promotes metastasis of colorectal cancer via targeting GEF-H1/RhoA axis. Theranostics. 2020;10(18):8211–26. https://doi.org/10.7150/thno.44419.
Gu C, Lu H, Qian Z. Matrine reduces the secretion of exosomal circSLC7A6 from cancer-associated fibroblast to inhibit tumorigenesis of colorectal cancer by regulating CXCR5. Biochem Biophys Res Commun. 2020;527(3):638–45. https://doi.org/10.1016/j.bbrc.2020.04.142.
Su Y, Lv X, Yin W, Zhou L, Hu Y, Zhou A, et al. CircRNA Cdr1as functions as a competitive endogenous RNA to promote hepatocellular carcinoma progression. Aging. 2019;11(19):8183–203. https://doi.org/10.18632/aging.102312.
Zhang H, Zhu L, Bai M, Liu Y, Zhan Y, Deng T, et al. Exosomal circRNA derived from gastric tumor promotes white adipose browning by targeting the miR-133/PRDM16 pathway. Int J Cancer. 2019;144(10):2501–15. https://doi.org/10.1002/ijc.31977.
This work was supported by Grants from the Natural Science Foundation of Zhejiang Provincial (Grant Nos. LY19H160014, LY20H130001, LQ21H130001), Medical and Health Research Project of Zhejiang Province (Grant Nos. 2019ZD018, 2021KY307), Ningbo Health Branding Subject Fund (Grant No. PPXK2018-02), Ningbo Natural Science Foundation (Grant Nos. 2018A610361, 2019A610319, 202003N4239), the Ningbo “Technology Innovation 2025” Major Special Project (Grant Nos. 2018B10015, 2020Z097), and the Key Project of Teaching and Research of Ningbo University (Grant No. JYXMXZD2021033).
This work was supported by grants from the Natural Science Foundation of Zhejiang Provincial (Grant Nos. LY19H160014, LY20H130001, LQ21H130001), Medical and Health Research Project of Zhejiang Province (Grant Nos. 2019ZD018, 2021KY307), Ningbo Health Branding Subject Fund (Grant No. PPXK2018-02), Ningbo Natural Science Foundation (Grant Nos. 2018A610361, 2019A610319, 202003N4239), the Ningbo “Technology Innovation 2025” Major Special Project (Grant Nos. 2018B10015, 2020Z097), and the Key Project of Teaching and Research of Ningbo University (Grant No. JYXMXZD2021033).
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Ye, D., Gong, M., Deng, Y. et al. Roles and clinical application of exosomal circRNAs in the diagnosis and treatment of malignant tumors. J Transl Med 20, 161 (2022). https://doi.org/10.1186/s12967-022-03367-x
- Malignant tumors