Arora Payal, Kim Eun-Ok, Jung Jin Kyu, Jang Kyung Lib
Division of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 609-735, Republic of Korea.
Cancer Lett. 2008 Mar 18;261(2):244-52. doi: 10.1016/j.canlet.2007.11.033. Epub 2007 Dec 31.
E-cadherin is a major cell adhesion molecule implicated as a potent tumor suppressor, which is frequently altered in human tumors including hepatocellular carcinoma. Here, we report that hepatitis C virus Core downregulates E-cadherin expression at the transcription level. This effect was abolished after treatment of 5'-Aza-2'dC, a specific inhibitor of DNA methyltransferase (DNMT). In addition, this repression was strongly correlated with hypermethylation of CpG islands of E-cadherin promoter via concerted action of both DNMT1 and 3b in Core-expressing cells. The decreased E-cadherin expression results in dramatic morphological changes in Core-expressing cells. In addition, Core-expressing cells aggregate poorly in suspension culture, reflecting their altered cell-cell interactions. The biological significance was further demonstrated by the increased collagen invasion ability of Core-expressing cells. Therefore, our finding suggests that Core plays a role in hepatocellular carcinogenesis by favoring cell detachment from the surrounding cells and migration outside of the primary tumor site.
E-钙黏蛋白是一种主要的细胞黏附分子,被认为是一种强大的肿瘤抑制因子,在包括肝细胞癌在内的人类肿瘤中经常发生改变。在此,我们报道丙型肝炎病毒核心蛋白在转录水平下调E-钙黏蛋白的表达。用DNA甲基转移酶(DNMT)的特异性抑制剂5'-氮杂-2'-脱氧胞苷处理后,这种效应被消除。此外,通过DNMT1和3b在表达核心蛋白的细胞中的协同作用,这种抑制与E-钙黏蛋白启动子的CpG岛高甲基化密切相关。E-钙黏蛋白表达的降低导致表达核心蛋白的细胞出现显著的形态变化。此外,表达核心蛋白的细胞在悬浮培养中聚集性差,反映了它们改变的细胞间相互作用。表达核心蛋白的细胞胶原侵袭能力增强进一步证明了其生物学意义。因此,我们的发现表明,核心蛋白通过促进细胞与周围细胞分离并从原发肿瘤部位向外迁移,在肝细胞癌发生中发挥作用。