Hu Li, Wang Wei, Cai Jinyang, Luo Jun, Huang Yi, Xiong Shilu, Li Wenxin, Guo Mingxiong
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei 430072;
Oncol Lett. 2013 Jul;6(1):49-54. doi: 10.3892/ol.2013.1318. Epub 2013 Apr 24.
Ovarian cancer is one of the most lethal gynaecological cancers worldwide. However, the mechanisms underlying ovarian carcinogenesis are not well understood. The present study used immunostaining, western blotting and quantitative real-time PCR to demonstrate that ZNF268 is overexpressed in human ovarian carcinomas. ZNF268-knockdown increased the viability, colony formation and growth of xenografts of ovarian carcinoma SKOV-3 cells, whereas SKOV-3 cell migration was inhibited. Furthermore, it was demonstrated that the knockdown of ZNF268 may increase SKOV-3 cell growth by promoting cell cycle progression. The findings suggest that ZNF268 is a novel protein involved in ovarian carcinogenesis and that it may aid in the understanding of the mechanisms of ovarian carcinogenesis.
卵巢癌是全球最致命的妇科癌症之一。然而,卵巢癌发生的潜在机制尚未完全明确。本研究采用免疫染色、蛋白质印迹法和定量实时聚合酶链反应来证明ZNF268在人类卵巢癌中过表达。敲低ZNF268可增加卵巢癌SKOV-3细胞异种移植瘤的活力、集落形成和生长,而SKOV-3细胞迁移则受到抑制。此外,研究表明敲低ZNF268可能通过促进细胞周期进程来增加SKOV-3细胞的生长。这些发现表明ZNF268是一种参与卵巢癌发生的新型蛋白质,可能有助于了解卵巢癌发生的机制。