- Open Access
LARP1 predict the prognosis for early-stage and AFP-normal hepatocellular carcinoma
© Xie et al.; licensee BioMed Central Ltd. 2013
- Received: 26 June 2013
- Accepted: 24 October 2013
- Published: 26 October 2013
The La-related protein 1 (LARP1) has been found to be a RNA binding protein and was related to spermatogenesis, embryogenesis and cell-cycle progression. The aim of this study was to investigate the prognostic value of LARP1 in hepatocellular carcinoma (HCC).
LARP1 expression was examined in 15 HCC cell lines and 272 clinical specimens using real-time PCR, immunohistochemistry (IHC) and western blot analysis (WB). LARP1 expression was also studied in 6 paired HCC lesions and the adjacent non-cancerous tissue samples. Statistical analyses were applied to derive association between LARP1 expression scores and clinical characters as well as patient survival.
mRNA and protein levels of LARP1 were higher in HCC cell lines and HCC lesions than in normal liver epithelial cells and the paired adjacent noncancerous tissues. LARP1 expression was correlated to survival time, vital status, tumor size and Child-Pugh score. Overall survival analysis showed HCC patients with high LARP1 expression level had lower survival rate (P < 0.01). Importantly, this correlation remained significant in patients with early-stage HCC or with normal serum AFP level.
LARP1 protein may represent a promising biomarker for predicting the prognosis of HCC, including in early-stage and AFP-normal patients.
- Hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is one of the most commonly diagnosed cancers and the third most common cause of cancer mortality worldwide. Despite great advances in surgical and medical management of the disease, relapse and metastasis are frequently observed in the clinic, and the long-term prognosis of patients with HCC is unsatisfactory. The development and progression of HCC is a multistage process involves molecular pathways and genetic abnormal changes. No specific signature of liver cancer gene expression has been reported to allow for patient-tailored therapy strategies. Hence, it is of great clinical value to further identify effective early markers for the diagnosis and prognosis of the disease as well as novel therapeutic targets.
The progression of HCC is thought to involve the deregulation of genes that are critical to cellular processes such as cell cycle control, cell growth, apoptosis, and cell migration and spreading. Clinically, prediction of prognosis plays an essential role in the assessment of HCC patients and optimal therapeutic options. As an increasing number of early-stage, small HCC nodules (< 3 cm) in patients with normal serum level of alpha fetal protein (AFP), a most commonly used diagnostic biomarker for HCC, prediction of prognosis of these patients represents a major challenge in the clinic. While tremendous effort has been made in identifying effective indicators for the prognostic prediction of these HCC, the availability of clinically applicable biomarkers remains limited. La-related protein 1 (Larp1) was first described in Drosophila and shown to be required for spermatogenesis, embryogenesis and cell cycle progression[3–5]. Phenotypically, loss of Larp1 causes an apoptosis, mitotic arrest and reduction in formation of migratory lamellipodia in cell. These data raise exciting questions about the role of Larp1 in mRNA translation and cell migration, and suggest Larp1 may have relevance in a number of conditions in which these processes are disrupted, such as in protein production and cancer.
In our current report, immunohistochemical analysis was performed to investigate the potential prognostic utility of LARP1 in a validation cohort of HCC in comparison with non-neoplastic liver tissues, including HCC patients with normal serum AFP level of early stage. Our data suggest that LARP1 might represent a valuable prognostic biomarker for HCC.
HCC cell lines, including QGY-7703, HCCC-9810, PLC/PRF5, SMMC-7721, Hep3B, HepG2, HuH7,HepG-2215, Bel-7402, QGY-7701, Bel-7404, HCCLM3, HCCLM6, MHCC97H and MHCC97L, were grown in Dulbecco’s modified Eagle’s medium (DMEM) (Invitrogen, Carlsbad, CA) supplemented with 10% fetal bovine serum (FBS) (Invitrogen). Immortalized normal liver epithelial cells, THLE3, were maintained in bronchial epithelial growth medium (Lonza Cologne GmbH, Walkersville, MD), with 5 ng/ml epidermal growth factor, 70 ng/ml phosphoethanolamine and 10% FBS, at 37°C in a humidified atmosphere containing 5% CO2.
Clinicopathological characteristics of clinical samples and expression of LARP1 in liver cancer
Vital status (at follow-up)
Death due to liver cancer
Expression of LARP1
RNA extraction, reverse transcription (RT) and real-time PCR
Total RNA from cultured cells was extracted using the Trizol reagent (Invitrogen, Carlsbad, CA) as the manufacturer instructed. cDNAs were amplified and quantified in ABI Prism 7500 Sequence Detection System (Applied Biosystems, Foster City, CA) using dye SYBR Green I (Invitrogen, Carlsbad, CA). The LARP1 primers designed using the Primer Express v 2.0 software (Applied Biosystems) are provided as following: forward: 5′- GCTGTTTAGGAACAGCTGCC -3′ and reverse: 5′- CCACAGGTGACAGGGAGAAG-3′. Expression data were normalized to the geometric mean of housekeeping gene GAPDH (forward: 5′-ACCACAGTCCATGCCATCAC-3′ and reverse: 5′-TCCACCACCCTG TTGCTGTA -3′) to control the variability in expression levels and calculated as 2-[(Ctof LARP1) – (Ctof GAPDH)], where Ct represents the threshold cycle for each transcript.
Total protein was prepared using the cell total protein extraction kits according to the manufacturer’s instruction (Millipore, Billerica, MA). Western blot was performed according to standard methods, using an anti-LARP1 antibody (Abcam, UK). Blotted membranes were stripped and re-probed with an anti-GAPDH antibody (Sigma, Saint Louis, MI) as a loading control.
The IHC procedure for LARP1 and scoring of LARP1 expression were performed as previously reported. IHC staining was quantitatively analyzed with the AxioVision Rel.4.6 computerized image analysis system assisted with the automatic measurement program (Carl Zeiss, Oberkochen, Germany). Briefly, the stained sections were evaluated at 200x magnification, and ten representative staining fields of each section were analyzed to produce Mean Optical Density value (MOD), which represented the strength of staining signals as measured per positive pixels. The MOD data were statistically analyzed using t-test to compare the average MOD difference between different groups of tissues. An optimal cutoff value was identified: the staining index score of > 6 was used to define tumors as high LARP1 expression and ≤ 6 as low expression of LARP1.
Gene Expression Omnibus database analysis
Gene Expression Omnibus database (GEO GSE25097) was used in the analysis of relationship of LARP1 expression and HCC.
All statistical analyses were carried out using the SPSS v. 13.0 statistical software packages (SPSS, Chicago, IL). Spearman’s correlation test was applied to analyze the correlation between LARP1 expression and clinic pathological characteristics. Survival curves were plotted by the Kaplan-Meier method and compared using the log-rank test. Independent prognostic factors were estimated by the Cox proportional hazards stepwise regression model. We first used SPSS statistic software to perform the Univariate analysis of each variance and found the factors which is significant different in the two groups and then perform the multivariate analysis. All P values were two-sided. A P value of less than 0.05 was considered statistically significant in all cases.
Upregulation of LARP1 in HCC cell lines and liver cancer lesions
Association between LARP1 expression and clinical features of liver cancer
Spearman analysis of correlation between LARP1 and clinicopathological factors
LARP1 expression level
Univariate and multivariate analyses of the prognostic power of LARP1
Univariate and multivariate analyses of various prognostic parameters in patients with liver cancer by Cox-regression analysis
95% confidence interval
95% confidence interval
Prognostic values of LARP1 in different HCC subgroups
To further demonstrate the value of LARP1 expression in predicting survival of HCC patients, multiple analysis methods were performed in this study. Firstly, as shown in Figure 2D, Kaplan-Meier and log-rank survival tests suggested that low- and high-LARP1 expression in HCC patients were associated with different survival time, with the OS of patients expressing low LARP1 in their HCC lesions surviving much longer that those with high LARP1 expression (P < 0.01). Interestingly, these patients with different OS could not be distinguished by conventional AFP test. While for the whole study cohort, the OS rates at 3, 5 and 8 years, respectively, were 46%, 37% and 33%, patients with high LARP1 protein levels had a significantly lowered 3, 5, 8-year survival rate than those with low LARP1 protein levels (14%, 10%, 7% vs 68%, 57%, 57%, respectively, P < 0.05).
In the present study, a cohort of patients (n = 272) were examined for LARP1 expression. Consistent results derived from three different assays strongly suggest a correlation between LARP1 level and the clinical outcome of HCC. Identification of LARP1 as a prognostic biomarker for HCC in our present study provides new opportunities in the clinic for prediction of patient survival. The findings that high LARP1 expression level is present in HCC cell lines and clinical lesions, as well as its correlation with the clinical staging of HCC, lay a foundation for developing this immunologically and pathologically detectable molecule into a clinically applicable approach to improved patient management based on more accurate judgment on disease prognosis.
LARP1 is on chromosome 5q33.2 possesses a signature La motif, which is an ancient RNA-binding domain, plus a second conserved motif. LARP1 appears to bind RNA in vitro via both the La motif and the LARP1 domain. Five LARP proteins exist in the human genome. LARP1 regulates negatively RAS-MAPK pathway and is shown to be involved in cell division, migration and apoptosis[6, 8]. LARP1 protein colocalizes with P bodies which function in RNA degradation. But the role of LARP1 in HCC is unclear. Our current study employed large numbers of patients in independent cohorts (n = 272). The consistency of the results of three assay methods (RT-PCR, immunoblotting and immunohistochemistry) and the repeat validations in the test as well as the independent validation cohort, provide with essential, reliable evidence for the clinical significance of LARP1 as a prognostic biomarker for HCC.
AFP is most commonly employed in the clinic for HCC screening and as an important predictor for patient survival after tumor resection[10–12] The diagnostic sensitivity of AFP for early HCC, however, is only 39–64% when used alone, leading to the unsatisfying reality that a large number of HCC patients without AFP elevation are missed and subsequently progress to late stage-HCC before becoming clinically symptomatic and detectable. Due to its low sensitivity in identifying new HCC cases that have not been detected by imaging technology previously, AFP has been shown to be only marginally effective in specific patient populations. Indeed, only 38.0% of HCC patients in our study cohorts are AFP-positive. By contrast, in the patient group in which AFP level was not predictive for prognosis, LARP1 appeared to be indicative of survival time lengths that are differential among the patients. Thus, our study has exhibited the potential value of LARP1 in predicting patient survival in subgroups with normal AFP levels or in the early-stage HCC group, which would have been difficult using currently clinically available surrogate biomarkers.
Studies have shown that for HCC early diagnosis and treatment strategies, such as surgical resection and liver transplantation, there is a longer survival time associated with patients who have a single HCC tumor nodule < 3 cm in diameter, or with patients carrying no more than 3 nodules with each smaller than 3 cm in diameter, giving rise to a reported 5-year survival of 50 to 70%[13, 14]. Using biomarkers to identify patients with a highest risk of developing worse prognosis may thus reduce mortality and medical costs. It is particularly noteworthy that in our test cohort, the patients with early HCC (TNM stages I-II) display a significantly higher levels (3–5 folds increase) of LARP1 in the HCC lesions than that in the normal liver tissue, and as the disease progresses to later stages, the LARP1 level increases further. In our validation cohort, early-stage (TNM stages I-II, tumor size less than 3 cm, single tumor nodule) HCC patients with low level of LARP1 protein immunostained also display a relative high OS than those diagnosed with late-stage HCC who carry high levels of LARP1 expression. In consistence with our observation, LARP1 has been mechanistically shown to promote cell invasion and metastasis. High potential of vascular invasion and metastasis is often the main biological basis for the poor prognosis of HCC. Thus, these characters of LARP1 thus warrant efforts to further explore the potential of LARP1 to become a promising biomarker for identifying patients with good prognosis after surgical excision in early stages. Inclusion of metastatic cases in future studies will help address whether a high-level expression of LARP1 in early-stage HCC patients may have the potential to progress to poor survival.
Several systems are available to classify HCC. Among them, the International Union Against Cancer’s TNM staging is one of the most prevalent. Although the TNM system has successfully graded patients on their prognosis according to clinicopathological variables, it is still limited in providing predictive information key to determining therapeutic strategies in subgroups of HCC patients, such as, prediction the prognosis of early-stage HCC. Thus, our current finding has provided evidence that the higher expression of LARP1 in HCC may be important for the detection of an aggressive phenotype or a phenotype predicting poor prognosis. We believe that the use of LARP1 protein as a diagnostic biomarker of HCC could improve the prospects of the early detection of HCC; and that an improved rate of detection would have important prognostic implications for patients with HCC. It is necessary to point out that our current study is of the retrospective nature and the number of patients with HCC lesions smaller than 3 cm was small. Clearly, further prospective studies designed to include a larger number of HCC lesions smaller than 3 cm and patients with metastasis are needed to validate the conclusions of this study. Moreover, it would be of great clinical value to determine the relationships of LARP1 with other signalling molecules and pathways which help us to better understand the molecular pathogenesis of these tumors and develop more effective targeted therapeutic strategies.
The study was supported by the National Science and Technology Major Project (2012ZX10002004), the Natural Science Foundation of China (No. 81101864), the Fundamental Research Funds for the Central Universities (12ykzs39), Sun Yat-Sen University Clinical Research 5010 Program (2007029), the 111 Project, Grant No. B12003.
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