Oncogenic HER2 fusions in gastric cancer
- De-Hua Yu†1,
- Lili Tang†1,
- Hua Dong1,
- Zhengwei Dong1,
- Lianhai Zhang2,
- Jiangang Fu1,
- Xinying Su1,
- Tianwei Zhang1,
- Haihua Fu1,
- Lu Han1,
- Liang Xie1,
- Hao Chen3,
- Ziliang Qian1,
- Guanshan Zhu1,
- Jia Wang1,
- Qingqing Ye1,
- Jingchuan Zhang1,
- Xiaolu Yin1,
- Xiaolin Zhang1,
- Jiafu Ji2 and
- Qunsheng Ji1, 4Email author
© Yu et al.; licensee BioMed Central. 2015
Received: 29 December 2014
Accepted: 25 March 2015
Published: 11 April 2015
Genetic amplification of HER2 drives tumorigenesis and cancer progression in a subset of patients with gastric cancer (GC), and treatment with trastuzumab, a humanized HER2-neutralizing antibody, improves the overall survival rate of HER2-positive patients. However, a considerable portion of the patients does not respond to trastuzumab and the molecular mechanisms underlying the intrinsic resistance to anti-HER2 therapy in GC is not fully understood.
We performed whole-transcriptome sequencing on 21 HER2-positive tumor specimens from Chinese GC patients. Whole genome sequencing was performed on the three samples with HER2 fusion to discover the DNA integration structure. A multicolor FISH assay for HER2 split screening was conducted to confirm HER2 fusion and IHC (HercepTest™) was used to detect the membranous expression of HER2. Fusion cDNA were transfected into NIH/3T3 cells and generate stable cell line by lentivirus. The expression of exogenous HER2 fusion proteins and pHER2 were examined by western blot analysis. In vitro efficacy studies were also conducted by PD assay and softagar assay in cell line expression wild type and fusion HER2. T-DM1 was used to assess its binding to NIH/3T3 cells ectopically expressing wild-type and fusion HER2. Finally, the anti-tumor efficacy of trastuzumab was tested in NIH/3 T3 xenografts expressing the HER2 fusion variants.
We identified three new HER2 fusions with ZNF207, MDK, or NOS2 in 21 HER2-amplified GC samples (14%; 3/21). Two of the fusions, ZNF207-HER2, and MDK-HER2, which are oncogenic, lead to aberrant activation of HER2 kinase. Treatment with trastuzumab inhibited tumor growth significantly in xenografts expressing MDK-HER2 fusion. In contrast, trastuzumab had no effect on the growth of xenografts expressing ZNF207-HER2 fusion, due to its inability to bind to trastuzumab.
Our results provide the molecular basis of a novel resistance mechanism to trastuzumab-based anti-HER2 therapy, supporting additional molecule stratification within HER2-positive GC patients for more effective therapy options.
KeywordsHER2 Fusion-gene Gastric cancer Trastuzumab Lapatinib
Gastric cancer (GC), as the second leading cause of cancer deaths worldwide, accounted for 989,600 new cases and 738,000 deaths globally in 2011 ; more than 50% of GC cases occur in Eastern Asia . The conventional treatments for GC include surgery, radiotherapy and chemotherapy , which have limited efficacy because most GC patients are in the advanced stages when diagnosed; the five-year survival rate for patients with stage III/IV GC is around 10% . Trastuzumab, a neutralization antibody of HER2, was recently approved for the treatment of a subset of advanced GC patients whose tumors are clinically defined as HER2-positive.
HER2 gene amplification was initially discovered as an oncogene in breast cancer (BC), which led to the development of HER2-targeted therapeutics for treating HER2-positive BC . These drugs include trastuzumab; lapatinib, a small-molecular inhibitor of HER2 kinase; pertuzumab, an antibody-blocking heterodimerization of HER2 with HER3; and trastuzumab emtansine (T-DM1), which is trastuzumab conjugated with the antimitotic agent emtansine (DM1). The clinical application of these targeted agents dramatically changed the landscape of BC therapy and exemplified a new era of personalized medicine associated with companion molecular diagnosis for patient selection [6-8]. In addition to BC, HER2 amplification and overexpression was also found in about 20% of GC patients . The anti-tumor activity of trastuzumab as a single agent or in combination with cytotoxic agents has been demonstrated in several HER2-positive human GC cell lines in vitro and in GC xenografts in vivo [10-12]. The preclinical efficacy translated into positive clinical trials in which a survival improvement was achieved in HER2-positive metastatic GC patients treated with trastuzumab plus cytotoxic agents [9,13]. These results led to the approval of trastuzumab as the first molecular targeted therapy for treating GC.
Despite the clinical benefits of trastuzumab in the treatment of patients with HER2-positive GC or BC [13,14], approximately 30-40% of HER2-positive tumors are insensitive to the treatment. Significant efforts to understand the resistance to anti-HER2 therapy in BC cases have recently been made, resulting in a diverse array of resistance mechanisms and clinical strategies to overcome the resistance . However, there is little understanding of the resistance mechanism to anti-HER2 therapy in GC. Therefore, we used a next-generation sequencing (NGS) approach to elucidate molecular insights in HER2-positive GC. In this study, for the first time, we report three HER2 gene fusions in HER2-positive GC in Chinese patients, and we characterize their oncogenic properties and sensitivity to anti-HER2 agents.
Human primary tumor samples
Specimens were collected during surgery from Chinese GC patients with postoperative pathological confirmation. The study was carried out at Peking University Cancer Hospital and Institute, and Shanghai Renji Hospital (2007 ~ 2010). Written informed consent was provided by each patient, and the study was approved by the ethics committees of the hospitals.
RNA-seq for transcriptome analysis
Total RNA was extracted using TRIzol (Life Technologies). All RNA samples showed RNA integrity numbers >7 (Agilent 2100 bioanalyzer).
Total RNA quality and concentration was measured using an RNA Pico chip on a Bioanalyzer 2100 (Agilent). Normalized starting quantities of total RNA were used to prepare Illumina sequencing libraries with a TruSeq™ RNA sample preparation kit (Illumina). The library preparation was performed according to the manufacturer’s instructions. The cDNA libraries were placed on an Illumina c-Bot for paired-end (PE) cluster generation, according to the protocol outlined in the Illumina HiSeq Analysis User Guide. The template cDNA libraries (1.5 μg) were hybridized to a flow cell, amplified, linearized, and denatured to create a flow cell with ssDNA ready for sequencing. Each flow cell was sequenced on an Illumina HiSeq2000 sequencing system. After a 100-cycle PE sequencing run, the bases and quality values were generated for each read with the current Illumina pipeline.
Detection of fusion transcripts
We sequenced each tumor sample up to an average of about 150× coverage. Fusion transcripts were detected using FusionMap software . Fusions supported by at least three reads were selected as candidates and subjected to RT-PCR and Sanger sequencing confirmation.
Quantification of mRNA expression level
N: number of reads mapped in gene
L: gene length (bp) (intron excluded)
R: number of raw reads
RT-PCR and Sanger sequencing
First strand cDNA synthesis was performed with 0.5 μg total RNA using a High Capacity cDNA Reverse Transcription kit (Life Technologies) according to the manufacturer’s instructions. PCR was performed in a 25-μL reaction mix containing 1× AmpliTaq Gold® 360 Master Mix (Life Technologies), 200 μM of each primer, and 2 μL of cDNA. The PCR cycling conditions were: 10-min incubation at 95°C, followed by 40 cycles of 94°C for 30 s, 60°C for 30 s, 72°C for 60 s, and a final incubation at 72°C for 10 min. The resulting PCR products were digested with ExoSAP-IT reagent (Affymetrix, Cleveland, OH) and then sequenced in forward and reverse directions with a BigDye Terminator Kit (Life Technologies) and an ABI 3730XL DNA analyzer (Life Technologies), following the manufacturer’s instructions. The sequencing data were analyzed for mutations after assembly and quality calling with SeqScape sequence analysis software (version 2.5; Life Technologies). The RT-PCR primers used for fusion gene confirmation were: 1) ZNF207/HER2, Forward: 5'-CTGAAGCCGTGGTGCTGGTATTGTA-3', Reverse: 5'-TGGGCATGTAGGAGAGGTCAGGTTT-3'; 2) MDK/HER2, Forward: 5'-GTTTGAGAACTGGGGTGCGTGTGAT-3', Reverse: 5'-AGACCATAGCACACT CGGGCACA-3'; 3) NOS2/HER2, Forward: 5’-CAAGCCCCACAGTGAAGAACATCTG-3', Reverse: 5'-TGCTGGAGGTAGAGTGGTGAACAGG-3'.
Whole genome sequencing
DNA was extracted from the frozen tissues using a Puregene DNA extraction kit (Qiagen) and quantified using a PicoGreen fluorescence assay (Qubit; Invitrogen). To conduct whole genome sequencing, 2 μg of DNA were required for each sample. After electrophoresis, DNA fragments of the desired length were gel purified. Adapter ligation and DNA cluster preparation were performed and subjected to Illumina Hiseq2000 sequencing. Two paired-end libraries with an insert size of 500 bp were prepared for all samples, after which four lanes from each library were subjected to whole genome sequencing. Raw image files were processed by Illumina Pipeline for base calling with default parameters, and the sequences of each individual were generated as 90-bp paired-end reads. Raw sequence data was mapped to the reference human genome (hg19) using Bowtie 2. The total mapping rate was >90%, and the average coverage was about 30×. Unmapped reads were then used to conduct genomic fusion detection with FusionMap .
Analysis of HER2, BRAF, KRAS, or PI3K mutations
HER2, BRAF, KRAS, and PIK3CA gene mutations from the RNAseq data were analyzed using ArrayStudio software (http://www.omicsoft.com/array-studio.php). Allele frequencies below 10% were removed in case of potential false positive. The mutation status was further confirmed by the whole genome sequencing data.
The primary antibodies used to detect the cytoplasmic domain of HER2 were purchased from Merck and Abcam, and the antibody used to detect the external domain of HER2 was purchased from Abnova. All of the collected tissues were fixed in FFPE blocks. Xenograft and cell-block sections were cut at 3 μm and human sections were cut at 4 μm for the HER2 IHC study. Paraffin sections were dewaxed and rehydrated in a Leica XL autostainer. Following antigen retrieval, the sections were incubated with 10 min of endogenous peroxidase block (DAKO), 60 min of primary antibodies, 30 min of EnVision System-HRP labeled polymer anti-mouse (DAKO), and 10 min of diaminobenzidine substrate (DAKO K3468), in that order. Finally, the sections were counter-stained, dehydrated, cleared, and mounted with coverslips in a Leica XL autostainer workstation. A HercepTest™ (DAKO) was used to detect the membranous expression of HER2, following standard procedures. Each slide was evaluated and scored on a 0–3 scale, following uniform guidelines developed for GC HER2 scoring from ToGA trials .
Fluorescent in situ hybridization (FISH)
A multicolor FISH assay for HER2 split screening was conducted via a dual-probe FISH break-apart test. The N-terminal and C-terminal probes for HER2 were generated internally by directly labeling BAC (N-terminal: RP11-98 J2; C-terminal: RP11-1044P23) DNA respectively with Green-dUTP (ENZO, Cat # 02 N32-050) and Red-dUTP (ENZO, Cat #02 N34-050). A CEP17 spectrum aqua probe (Vysis, Cat #32-131017) for the centromeric region of chromosome 17 was used as an internal control of the HER2 break-apart probes. Multicolor FISH was also used to confirm HER2 gene fusion with certain partner genes. The ZNF207 and NOS2 FISH probes were generated internally by directly labeling BAC (ZNF207: RP11-55 J8; NOS2: RP11-696H14) DNA with gold 525-dUTP (ENZO, Cat #ENZ42843). The FISH assays were performed as previous reported . Briefly, the assay was run on 4-μm dewaxed and dehydrated FFPE TMAs. A SPoT-Light tissue pretreatment Kit (Invitrogen, Cat #00-8401) was used for the pretreatment (boiled in reagent 1 for ~18 minutes, then coated with reagent 2 for ~14 minutes, minor time adjustments were made for individual samples). The sections and probes were co-denaturated at 79°C for 6 minutes and then hybridized at 37°C for 48 hours. After a quick post wash off process (0.3% NP40/2xSSC at 75.5°C for 2 minutes, twice in 2 × SSC at room temperature for 2 minutes), the sections were mounted with 0.3 μg/ml DAPI (Vector, Cat #H-1200) and stored at 4°C, avoiding light for at least 30 minutes prior to observation. The FISH signals were observed using a fluorescence microscope equipped with the appropriate filters, allowing visualization of the intense red/green/gold signals of the target genes, the intense aqua centromere signals, and the blue counterstained nuclei. A minimum 100 nuclei were scored for each sample. Only nuclei with a minimum of two green and two red signals were scored. In the break-apart assay, fused N-terminal (green) and C-terminal (red) signals represent a normal HER2 gene. HER2 amplification status was defined as a ratio of fused HER2 signals to CEP17 (aqua) ≥2. The following situations indicated the presence of HER2-involved fusion: 1) broken apart: more than one set of broken-apart N-terminal and C-terminal signals in ≥10% tumor cells; 2) N-terminal deletion: more C-terminal signals in addition to fused and/or broken-apart signals in ≥30% tumor cells. Then, a multicolor FISH assay was performed on HER2 broken apart or N-terminal-deleted positive cases. The HER2 fusion was confirmed when HER2 C-terminal red signals co-localized with a certain partner gene’s gold signals.
Vector construction, cell culture, transduction, and transformation studies
ZNF207-HER2 and MDK-HER2 fusion cDNA were synthesized (Additional file 1: Files S1 and S2) at Generay (Shanghai, China). The products were subcloned into PLVX lentiviral vector (Sunbio, China). The integrity of the inserted cDNA was verified by Sanger sequencing of the constructs. Lentiviruses expressing ZNF207-HER2 and MDK-HER2 fusions were produced according to the manufacturer’s instructions. NIH/3 T3 fibroblast cells were infected with lentiviruses expressing empty vector, and ZNF207-HER2 and MDK-HER2 fusions were treated with puromycin (2 μg/ml) for two weeks. NIH/3 T3-resistant cells were seeded on 96-well plates (2000 cells/well) in 0.33% agar in complete medium. The expression of exogenous HER2, ZNF207-HER2, and MDK-HER2 proteins and phosphorylation of HER2 were examined by immune blot analysis. The overnight cell cultures in liquid or soft agar medium were treated with lapatinib, T-DM1 (synthesized at ChemPartner, Shanghai, China) for 3 and 14 days, respectively. The cell growth rate was measured by MTS assay according to the manufacturer’s instructions (Promega).
Total cellular extracts from the cell lines were prepared in an SDS lysis buffer supplemented with protease inhibitors and phosphatase inhibitors (Sigma). Protein samples were fractionated by SDS-PAGE and blotted onto polyvinylidene difluoride membranes (Millipore). After incubation with the indicated antibodies at 4°C overnight, the blots were detected with the relevant horseradish peroxidase-conjugated anti-mouse or anti-rabbit IgG antibody and enhanced chemilluminescence (GE Healthcare). The antibody information used in the Western blot assays are included were as follows: pHER2 (Y1221/1222) (CST, Cat #2243, diluted 1:1000); HER2 (CST, Cat #2165, diluted 1:1000); pErk1/2 (T202/Y204) (CST, Cat #4376, diluted 1:1000); Erk1/2 (CST, Cat #9102, diluted 1:1000); pAKT (Ser473) (CST, Cat# 9271, diluted 1:1000); and AKT (CST, Cat #9272, diluted 1:1000).
Trastuzumab emtansine (T-DM1) receptor binding assay
Approximately 5 × 105 NIH/3T3 cells expressing vector control, wild-type HER2, ZNF207-HER2, or MDK-HER2 were collected using enzyme-free cell dissociation buffer (Invitrogen). After blocking with 10% donkey serum for 30 minutes at 4°C, the cells were incubated with 10 μg/mL T-DM1 (ChemPartner) at 4°C for one hour. The cells were rinsed three times with wash buffer (0.5% BSA in PBS) and further incubated with 10 ug/mL Alex488 labeled donkey anti-human IgG (Jackson immunology) at 4°C for one hour. After rinsing five times with wash buffer, the mean intensity of the fluorescence was detected by FACSCanto (BD). The receptor binding was qualitatively evaluated by the peak shift in the histogram.
In vivo efficacy study in xenograft models
6- to 8-week-old female nude (nu/nu) mice (Vital River, Beijing, China) were used for in vivo efficacy studies. All experiments using immunodeficient mice were carried out in accordance with the guidelines approved by the Institutional Animal Care and Use Committees. NIH/3 T3 cells expressing ZNF207-HER2, MDK-HER2, or a control vector were inoculated subcutaneously into female nude mice. Tumor-bearing mice with tumors ranging 100–200 mm3 in size were selected randomly and placed in groups according to their tumor volume and body weight (eight animals per group) for treatment. Trastuzumab (15 mg/kg) was administrated by intravenous injection twice a week. The xenograft tumors were measured in two perpendicular diameters with a caliper, and tumor volumes (TV) were calculated using the formula TV = (length × width2)/2. Percentage of tumor growth inhibition (%TGI) was calculated using the formula [1-(change of tumor volume in treatment group/change of tumor volume in control group)] × 100, and was used to evaluate anti-tumor efficacy. Student’s t tests were used to compare the TGI of the treatment group with that of the control group. Statistical tests were two sided, with P < 0.05 considered significant.
Novel HER2 fusion genes identified in HER2-positive gastric cancer
A summary of patients with gastric cancer harboring HER2 fusions
Amplification and overexpression of the HER2 fusions in GC
In the GC196 sample, over 100 reads were detected for ZNF207 genomic sequences only composing the 5’ partner and HER2 sequences only composing the 3’ partner of the ZNF207-HER2 fusion; low reads (~20) were captured for the genomic sequences outside the fusion gene. In the GC334 specimen, in addition to the high reads (>1800) of the fusion partners of NOS2-HER2 fusion that were detected, an average of 500 reads was also captured for the entire genomic sequence of wild-type HER2 gene.
A summary of the HER2 fusion status
5' fusion partner status
N Ter AMP
C Ter AMP
N Ter AMP
Together, these data demonstrate the gene amplification of the HER2 fusions, which correlated with dis-regulation of both mRNA and protein expressions of the fusion variants. In addition, the HercepTest™ did not distinguish the fusion proteins from the wild-type HER2.
Oncogenic driver activity of the HER2 fusions
A number of genetic aberrations with oncogenic properties have been reported recently in GC cases . Thus, we aimed to determine whether the HER2 fusions overlapped with the known oncogenic alterations. RNAseq and WGS data showed that the three HER2-fusion-positive GC patients were negative for HER3, BRAF, KRAS, PI3KCA, and HER2 mutations, and negative for amplifications of FGFR2 and cMET (data no shown), which are common genetic alterations identified in GC . The mutually exclusive nature of HER2 fusions from these known oncogenic alterations suggests that the HER2 fusions are oncogenic drivers. In addition, sequence analysis revealed that proteins encoded by ZNF207-HER2 and MDK-HER2 fusion variants contained a partial extracellular domain, a transmembrane domain, and a full kinase domain of HER2 (Additional file 1: Files S1 and S2), whilst the predicated fusion protein of NOS2-HER2 would be a full-length HER2 protein as result of a stop codon that is introduced prior to the HER2 start codon (Additional file 1: File S3). Based on the sequence predication that NOS2-HER2 fusion encodes a full-length HER2 without NOS2, our efforts on function characterization of these HER2 fusion proteins were then focused on ZNF207-HER2 and MDK-HER2 fusions.
In addition to the induction of phosphorylation of Tyr1221/1222, the exogenous expression of ZNF207-HER2 or MDK-HER2 fusions in NIH/3 T3 cells also induced transformational morphology (Figure 5B); anchorage-independent growth of the cells in vitro, which was comparable to the oncogenic phenotypes caused by mutant KRAS (V12D) (Figure 5C). Together, these results demonstrate the oncogenic properties of the ZNF207-HER2 and MDK-HER2 fusions in GC.
Different binding and responsiveness of the HER2 fusions to T-DM1 and trastuzumab
In summary, our results clearly demonstrate that the ZNF-207-HER2 fusion does not respond to trastuzumab, due to the loss of its binding ability.
Several studies have recently used NGS to understand the molecular basis of GC, and a number of previously unknown genetic alterations have been reported , including genetic fusions of HER2 in human GC cell lines. For example, two HER2 fusions were identified at the same time in human GC cell line MKN7 (HER2 positive): a fusion between CDK12 exon 12 and HER2 intron 4, and a second fusion between NEUROD2 exon 1 and HER2 exon 8 . However, there was no direct evidence in that report that demonstrated the oncogenic driver of these HER2 fusions. In the current study, we performed a whole-transcriptome sequencing of 21 HER2-positive GC tumor samples taken from Chinese patients, and discovered three HER2 fusion transcripts due to HER2 gene fusions. Two of them, ZNF207-HER2 and MDK-HER2 were truncated in the N-terminal extracellular domains, but they remained intact in the kinase and transmembrane domains of HER2. The amplification and overexpression of the three HER2 gene fusions were detected in the primary GC samples by multicolor FISH and RNAseq or IHC-based HercepTest™ analysis. The ectopic expression of ZNF207-HER2 and MDK-HER2 in the NIH/3T3 cells led to a constitutive activation of HER2 and downstream signaling, and thus, cell transformation in vitro and tumorigenesis in vivo, demonstrating the oncogenic driver of the fusions. Furthermore, the xenografts ectopically expressing MDK-HER2 but not ZNF207-HER2 were sensitive to trastuzumab. Interestingly, the HER2 fusions were found to be mutually exclusive with mutations of PI3KCA, BRAF, KRAS, and HER3 and amplifications of FGFR2 and c-MET. Collectively, our data confirmed for the first time the presence of oncogenic HER2 arrangements in patients with GC. The ZNF207-HER2 fusion represents a novel intrinsic resistance mechanism to trastuzumab-based anti-HER2 therapy, due to the loss of binding ability to trastuzumab.
Despite the overall survival benefit achieved with trastuzumab in GC patients carrying HER2 amplification, a significant portion of the patients do not respond clinically to the treatment, and there is little understanding of the molecular mechanism underlying this intrinsic resistance. In contrast, the understanding of the mechanisms of both intrinsic and acquired resistance to HER2 inhibitors in HER2-positive BC is far more advanced [15,23]. For example, some intrinsic resistance mechanisms affect the ability of HER2 inhibitors to directly engage HER2 in BC; a truncated form of HER2, p95, lacking the trastuzumab binding region [24,25]; a splice variant that eliminates exon 16 (HER2-Δ16) in the extracellular domain of the HER2 receptor, preventing disruption of HER2 homodimers upon binding by trastuzumab ; In our study, we did not assess p95, but we did find HER2-Δ16 in a GC tumor sample, which naturally harbored HER2-Δ16. Surprisingly, its corresponding patient-derived gastric cancer xenograft (PDGCX), which retains HER2-Δ16 (data not shown), responded well to trastuzumab treatment, with a significant tumor regression being observed (data not shown). Given the lack of clinical evidence of association between HER2-Δ16 and resistance to trastuzumab in BC, as well as the lack of preclinical data on the anti-tumor efficacy of trastuzumab in xenografts carrying HER2-Δ16 , our data suggest that HER2-Δ16 was not a resistance mechanism to trastuzumab in GC when tested in the PDGCX model. Additional HER2-Δ16 positive PDGCX models are warranted to confirm this observation further.
Surprisingly, in addition to the HER2 fusions, we also found two recurrent in-frame BRAF fusion transcripts, BAIAP2L1-BRAF (data not shown), in another cohort of HER2-amplified GC patients. Although further work is needed to demonstrate its oncogenic activity and sensitivity to trastuzumab or BRAF inhibitor, the findings suggest that BAIAP2L1-BRAF could be a potential resistance mechanism to trastuzumab, as it maintains an intact BRAF kinase domain .
The current clinical protocol for selecting HER2-positive patients is based on FISH positivity or an IHC (HercepTest™) score of 3+ (HercepTest™ score of 2+ needs further FISH confirmation). HER2 gene amplification is determined by the ratio between the numbers of signals from the hybridization of the HER2 gene probe (covers the whole HER2 gene) and the number of signals from the hybridization of the reference chromosome 17 centromere probe . The antibody used in the HercepTest™ recognizes the HER2 epitope located at the HER2 intracellular site, which is also covered by all three HER2 fusions (Figure 1A). Therefore, the current HER2 tests cannot distinguish between the amplifications of the HER2 fusions and that of the wild-type. The use of multicolor FISH and RT-PCR assays to detect the HER2 fusions developed in this study demonstrated the feasibility of detecting HER2 fusions as clinical biomarkers in either FFPE or frozen surgical GC specimens. This finding warrants further clinical validation of the novel resistant mechanism of the ZNF207-HER2 fusion to trastuzumab-based therapy.
In addition to the antibody, a number of small-molecule HER2 kinase inhibitors are available: lapatinib, an approved agent for HER2-positive BC patients, and afatinib and neratinib, two irreversible kinase inhibitors, currently in phase III clinical trials for HER2-positive BC. The modulation of AKT signaling by lapatinib in the cells expressing the HER2 fusions (Figure 5A) suggests that the small-molecule inhibitor against HER2 kinase is a potential option for cancer patients with the HER2 fusions. This notion is further supported by our observations that NIH/3T3 cells expressing either ZNF207-HER2 or MDK-HER2 showed to be sensitivity to lapatinib, afatinib, and neratinib in vitro (data not shown).
Besides the functional and phonotypical heterogeneity, emerging evidences indicate that genetic heterogeneity among tumor cells contributes to the advantages for survival, proliferation, metastasis and resistance to anti-cancer therapies. Recently, Tajiri et al. examined 475 GC samples using multiple ligation-dependent probe amplification (MLPA) and FISH analysis and revealed intratumoral heterogeneity of HER2 amplification in 41% (21/51) of HER2-amplified tumors. The mutually exclusive co-amplification of HER2 with EGFR, FGFR2, FGFR2 and MET was also observed respectively in some of the tumors, suggesting the potential challenges for design of targeted-therapy approaches . The homogenous expression of ZNF270-HER2 supports the driver role of this fusion gene, which is consistent with our experimental results. However, the advantage of co-amplification of MDK-HER2 and NOS2-HER2 with wild HER2 (intra-tumor heterogeneity) is yet to be uncovered. Further studies to explore the responsiveness of the HER2 fusions to combination of trastuzumab with pertuzumab or chemotherapies may lead to additional insights into the impact of the HER2 fusions to anti-HER2 therapies.
It is noteworthy that the HER2 positive GC samples used for this study were collected prior the introduction of trastuzumab to China, thus we lack evidence for clinical response of the tumors harboring HER2 fusions to trastuzuamb. Further studies on GC samples from patients treated with trastuzumab at different stages will help to confirm the effect of the HER2 fusions to trastuzmab therapy and their oncogenic property.
Although further large-scale clinical investigations are needed to understand the clinical prevalence in GC patients, our data on ZNF207-HER2, along with the discovery of two recurrent BAIAP2L1-BRAF, strongly indicate a large degree of molecular heterogeneity, even in the well-defined HER2-positive segment, representing potential de novo resistance to trastuzumab-based GC therapies. In addition, whether a similar mechanism would exist in BC also needs to be exploited.
In summary, we uncovered three previously unidentified HER2 fusion genes in GC patients whose tumors were clinically classified as HER2-positive. Our results suggest that these HER2 fusions are genetically amplified driver oncogenes that respond differently to the HER2-neutralizing antibody trastuzumab. The resistance of ZNF207-HER2 to trastuzumab and the existence of the recurrent BRAF fusion variants warrant molecular subtype diagnoses of HER2-positive GC patients for more effective personalized trastuzumab therapies and for future treatment options.
The authors thank Charles Liu, Peter Lu and Jingyan Ding for assistance in data generation, analysis and interpretation; Jie Zang for editing, review, revision of the manuscript.
This work was sponsored by AstraZeneca
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