Liver Cancer Institute and Zhongshan Hospital, Institutes of Biomedical Sciences, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai 200032, P.R. China.
Oncol Rep. 2013 Dec;30(6):2795-803. doi: 10.3892/or.2013.2737. Epub 2013 Sep 19.
Osteopontin (OPN) may facilitate tumorigenesis and metastasis through prevention of tumor cells from apoptosis. Although previous studies have suggested involvement of enhanced Bcl-2 protein family expression, the role of OPN together with Bcl-2 in hepatocellular carcinoma (HCC) remains unknown. In this study, we used western blotting to detect the OPN and Bcl-2 expression levels in cell lines with different OPN backgrounds and HCC tissues, and tumor tissue microarrays to examine OPN and Bcl-2 expression levels in 454 HCC cases. The Kaplan-Meier method and log-rank test were applied to investigate the predictive values of OPN and Bcl-2 in HCC patients. In vitro assays indicated that OPN expression increased concordantly with increasing metastatic potential in MHCC97-H, MHCC97-L, HepG2 and SMMC-7721 cell lines by western blotting, whereas Bcl-2 expression declined. In addition, Bcl-2 was highly upregulated in OPN knockdown MHCC97-H cell lines. Furthermore, in HCC tissues, it was confirmed that OPN levels were also significantly higher in recurrent tumor tissues compared to non-recurrent tissues by western blotting (p<0.001), whereas the contrary occurred in Bcl-2 (p=0.046). Using immunohistochemistry analysis, patients with higher OPN levels had significantly shorter median survival time and recurrence time compared to the lower ones, although the opposite occurred in Bcl-2 levels. Of note, when OPN and Bcl-2 were combined, we found that the co-index of OPN/Bcl-2 was an independent prognostic factor for both overall survival (p<0.001) and time to recurrence (p<0.001). Our findings demonstrate that OPN/Bcl-2 expression is a promising independent predictor of recurrence and survival in HCC. Additionally, Bcl-2 levels may be regulated by OPN in the HCC microenvironment.
骨桥蛋白(OPN)可能通过防止肿瘤细胞凋亡来促进肿瘤的发生和转移。虽然之前的研究表明 Bcl-2 蛋白家族表达增强参与其中,但 OPN 与 Bcl-2 在肝细胞癌(HCC)中的作用仍不清楚。在这项研究中,我们使用 Western blot 检测了具有不同 OPN 背景的细胞系和 HCC 组织中的 OPN 和 Bcl-2 表达水平,并使用 HCC 组织微阵列检测了 454 例 HCC 病例中的 OPN 和 Bcl-2 表达水平。Kaplan-Meier 方法和对数秩检验用于研究 OPN 和 Bcl-2 在 HCC 患者中的预测价值。体外实验表明,Western blot 检测结果显示,MHCC97-H、MHCC97-L、HepG2 和 SMMC-7721 细胞系中 OPN 表达增加与转移能力增强一致,而 Bcl-2 表达下降。此外,在 OPN 敲低的 MHCC97-H 细胞系中,Bcl-2 高度上调。此外,在 HCC 组织中,Western blot 检测结果显示,与非复发性组织相比,复发性肿瘤组织中的 OPN 水平也明显更高(p<0.001),而 Bcl-2 则相反(p=0.046)。使用免疫组织化学分析,我们发现 OPN 水平较高的患者中位生存时间和复发时间明显短于 OPN 水平较低的患者,而 Bcl-2 水平则相反。值得注意的是,当 OPN 和 Bcl-2 结合时,我们发现 OPN/Bcl-2 共同指数是 HCC 患者总生存(p<0.001)和复发时间(p<0.001)的独立预后因素。我们的研究结果表明,OPN/Bcl-2 表达是 HCC 复发和生存的有前途的独立预测因子。此外,Bcl-2 水平可能在 HCC 微环境中受 OPN 调节。