Sheng Xu-Ren, Xing Song-Ge, Wang Run-Dong, Chen Kang, Jia Wei-Dong
Department of Liver Surgery, Affiliated Provincial Hospital, Anhui Medical University.
Anhui Province Key Laboratory of Hepatopancreatobiliary Surgery.
Onco Targets Ther. 2018 Feb 21;11:909-917. doi: 10.2147/OTT.S153381. eCollection 2018.
The tumor suppressor candidate 3 () has been considered to be closely associated with the occurrence, development and invasion of various malignant tumors. However, the expression of in hepatocellular carcinoma (HCC) tissues remains ambiguous. The purpose of this research was to investigate the expression of in HCC tissues and analyze the relationship between levels and clinicopathological characteristics and prognosis of HCC patients.
Immunohistochemistry was used to detect the expression of in HCC and the corresponding para-cancerous tissues from 92 samples of HCC patients. mRNA and protein expression levels of were evaluated by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot assays in 25 paired HCC and corresponding adjacent nontumor tissues. Furthermore, statistical analysis was applied to evaluate the correlation between level and the clinicopathological features and prognosis of HCC patients.
Immunohistochemical assay indicated that the expression of was significantly lower in HCC tissues when compared with the corresponding para-cancerous tissues (=11.512, =0.001). The analysis of clinicopathological characteristics showed that low expression of in HCC tissues was significantly associated with Edmondson grade, Barcelona Clinic Liver Cancer stage and tumor size (=0.008, 0.009 and 0.020, respectively). Univariate analysis showed that the expression of was strongly correlated with overall survival (OS) and disease-free survival (DFS) after radical surgery in HCC patients (<0.001, <0.001, respectively). Multivariate analysis revealed that the level was an independent risk factor for OS and DFS in HCC patients (=0.001, <0.001, respectively). Results of qRT-PCR and Western blot assays indicated that the level of in HCC tissues was significantly lower than that in the corresponding adjacent noncancerous tissues (<0.01, <0.001).
The expression of in HCC was significantly downregulated and was correlated with tumor progression and prognosis, which could be used as an independent predictor of prognosis in HCC patients.
肿瘤抑制候选基因3()被认为与多种恶性肿瘤的发生、发展及侵袭密切相关。然而,其在肝细胞癌(HCC)组织中的表达仍不明确。本研究旨在探讨其在HCC组织中的表达情况,并分析其水平与HCC患者临床病理特征及预后的关系。
采用免疫组织化学法检测92例HCC患者的HCC组织及相应癌旁组织中 的表达。通过定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法(Western blot)检测25对配对的HCC组织及相应的癌旁非肿瘤组织中 的mRNA和蛋白表达水平。此外,应用统计学分析评估 水平与HCC患者临床病理特征及预后的相关性。
免疫组织化学检测显示,与相应癌旁组织相比,HCC组织中 的表达显著降低(=11.512,=0.001)。临床病理特征分析表明,HCC组织中 低表达与Edmondson分级、巴塞罗那临床肝癌分期及肿瘤大小显著相关(分别为=0.008、0.009和0.020)。单因素分析显示, 在HCC患者根治性手术后的总生存期(OS)和无病生存期(DFS)中密切相关(分别为<0.001,<0.001)。多因素分析显示, 水平是HCC患者OS和DFS的独立危险因素(分别为=0.001,<0.001)。qRT-PCR和Western blot检测结果表明,HCC组织中 的水平显著低于相应的癌旁非癌组织(<0.01,<0.001)。
在HCC中的表达显著下调,且与肿瘤进展及预后相关,可作为HCC患者预后独立预测指标。