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新型基因URG4增强胃癌细胞的存活能力。

Enhanced cell survival of gastric cancer cells by a novel gene URG4.

作者信息

Song Jiugang, Xie Huahong, Lian Zhaorui, Yang Guitao, Du Rui, Du Yulei, Zou Xue, Jin HaiFeng, Gao Juan, Liu Jie, Fan Daiming

机构信息

State Key Laboratory of Cancer Biology and Institute of Digestive Diseases, Xijing Hospital, The Fourth Military Medical University, Xi'an 710032, Shaanxi Province, PR China.

出版信息

Neoplasia. 2006 Dec;8(12):995-1002. doi: 10.1593/neo.06592.

Abstract

Upregulated gene 4 (URG4), a novel gene located on 7 chromosome (7p13), was found to contribute to hepatocarcinogenesis. However, the role of URG4 in the gastric carcinogenesis still remains unclear. In the present study, URG4 was found by immunohistochemistry to be upregulated in human gastric cancer tissues compared with matched adjacent nonneoplastic tissues. The proliferating cell nuclear antigen index is higher in gastric cancer tissues with high URG4 expression than in those with low URG4 expression. The growth of GES-1 cells, which are immortalized human gastric epithelial mucosa cells with baseline URG4 expression, was accelerated by URG4 induction. Downregulation of URG4 through URG4 small interfering RNA (siRNA) in SGC7901 and MKN28 cells, which had high endogenous URG4 expression, suppressed cell proliferation in both of these cells. URG4-siRNA also inhibited the proliferation of SGC7901 and MKN28 cells in soft agar and tumor formation in nude mice. Overexpression of URG4 in GES cells upregulated cyclin D1, whereas repression of URG4 in SGC7901 and MKN28 cells downregulated cyclin D1. The data suggested that URG4 played an important role in the development of human gastric cancer by regulating the expression of cyclin D1 and might be used as a potential therapeutic target for gastric cancer.

摘要

上调基因4(URG4)是一个位于7号染色体(7p13)上的新基因,已发现其与肝癌发生有关。然而,URG4在胃癌发生中的作用仍不清楚。在本研究中,通过免疫组织化学发现,与配对的相邻非肿瘤组织相比,URG4在人胃癌组织中表达上调。URG4高表达的胃癌组织中增殖细胞核抗原指数高于URG4低表达的组织。具有基线URG4表达的永生化人胃上皮黏膜细胞GES-1细胞的生长因URG4诱导而加速。在具有高内源性URG4表达的SGC7901和MKN28细胞中,通过URG4小干扰RNA(siRNA)下调URG4可抑制这两种细胞的增殖。URG4-siRNA还抑制了SGC7901和MKN28细胞在软琼脂中的增殖以及裸鼠体内的肿瘤形成。GES细胞中URG4的过表达上调了细胞周期蛋白D1,而SGC7901和MKN28细胞中URG4的抑制下调了细胞周期蛋白D1。数据表明,URG4通过调节细胞周期蛋白D1的表达在人胃癌发展中起重要作用,可能作为胃癌的潜在治疗靶点。

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