Guo Wei, Dong Zhiming, Guo Yanli, Shen Supeng, Guo Xin, Kuang Gang, Yang Zhibin
Laboratory of Pathology, Hebei Cancer Institute, the Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Mol Carcinog. 2016 Nov;55(11):1655-1666. doi: 10.1002/mc.22416. Epub 2015 Oct 12.
The RAS-association domain family (RASSF) consists of 10 members, and several members act as tumor suppressor genes and epigenetically inactivated in different tumor types. The present study investigated the role and methylation status of RASSF2, RASSF3, RASSF4, and RASSF6 in the pathogenesis and prognosis of GCA. Quantitative real-time RT-PCR, Western blot, and immunohistochemistry (IHC) methods were used respectively to detect the expression of RASSF2, RASSF3, RASSF4, and RASSF6 in 135 GCA cases and BS-MSP method was used to clarify the methylation status of these four genes. Decreased mRNA and protein expression of RASSF2, RASSF3, RASSF4, and RASSF6 were detected in GCA tumor tissues. Aberrant CpG island methylation of RASSF2, RASSF4, and RASSF6 were detected in GCA tumor tissues and were inversely correlated with the expression levels of these genes. Both of RASSF2 and RASSF6 expression and methylation were associated with TNM stage, depth of invasion, LN metastasis, distant metastasis or recurrence, and UGIC family history. GCA patients with simultaneous negative protein expression of RASSF2 and RASSF6 or with simultaneous methylation of both genes demonstrated poor patient survival. These results suggest that down-regulation of RASSF2, RASSF3, RASSF4, and RASSF6 is a tumor-specific phenomenon and the inactivation of RASSF2 and RASSF6 may be associated with tumor progression. Inactivation of RASSF2, RASSF4, and RASSF6 through CpG island methylation may play important roles in GCA carcinogenesis. A combination of RASSF2 and RASSF6 expression or hypermethylation may serve as useful prognostic biomarker for GCA. © 2015 Wiley Periodicals, Inc.
RAS 关联结构域家族(RASSF)由 10 个成员组成,其中几个成员作为肿瘤抑制基因,在不同肿瘤类型中发生表观遗传失活。本研究调查了 RASSF2、RASSF3、RASSF4 和 RASSF6 在巨细胞动脉炎(GCA)发病机制和预后中的作用及甲基化状态。分别采用定量实时 RT-PCR、蛋白质免疫印迹法和免疫组织化学(IHC)方法检测 135 例 GCA 病例中 RASSF2、RASSF3、RASSF4 和 RASSF6 的表达,并采用亚硫酸氢盐修饰后测序 PCR(BS-MSP)方法阐明这四个基因的甲基化状态。在 GCA 肿瘤组织中检测到 RASSF2、RASSF3、RASSF4 和 RASSF6 的 mRNA 和蛋白质表达降低。在 GCA 肿瘤组织中检测到 RASSF2、RASSF4 和 RASSF6 的 CpG 岛异常甲基化,且与这些基因的表达水平呈负相关。RASSF2 和 RASSF6 的表达及甲基化均与 TNM 分期、浸润深度、淋巴结转移、远处转移或复发以及上消化道癌家族史相关。同时 RASSF2 和 RASSF6 蛋白表达均为阴性或两个基因均发生甲基化的 GCA 患者生存情况较差。这些结果表明,RASSF2、RASSF3、RASSF4 和 RASSF6 的下调是一种肿瘤特异性现象,RASSF2 和 RASSF6 的失活可能与肿瘤进展有关。通过 CpG 岛甲基化使 RASSF2、RASSF4 和 RASSF6 失活可能在 GCA 致癌过程中起重要作用。RASSF2 和 RASSF6 表达或高甲基化的联合检测可能作为 GCA 有用的预后生物标志物。© 2015 威利期刊公司