Department of Microbiology/Key Laboratory for Experimental Teratology of Chinese Ministry of Education, School of Medicine, Shandong University, 44# Wenhua Xi Road, Jinan 250012, PR China.
Biochem Biophys Res Commun. 2011 Dec 16;416(3-4):372-8. doi: 10.1016/j.bbrc.2011.11.045. Epub 2011 Nov 19.
Epigenetic alterations such as aberrant expression of histone-modifying enzymes have been implicated in tumorigenesis. Jumonji domain containing 2B (JMJD2B) is a newly identified histone demethylase that regulates chromatin structure or gene expression by removing methyl residues from trimethylated lysine 9 on histone H3. Recent observations have shown oncogenic activity of JMJD2B. We explored the functional role of JMJD2B in cancer cell proliferation, survival and tumorigenesis, and determined its expression profile in gastric cancer. Knocking down JMJD2B expression by small interfering RNA (siRNA) in gastric and other cancer cells inhibited cell proliferation and/or induced apoptosis and elevated the expression of p53 and p21(CIP1) proteins. The enhanced p53 expression resulted from activation of the DNA damage response pathway. JMJD2B knockdown markedly suppressed xenograft tumor growth in vivo in mice. Moreover, JMJD2B expression was increased in primary gastric-cancer tissues of humans. Thus, JMJD2B is required for sustained proliferation and survival of tumor cells in vitro and in vivo, and its aberrant expression may contribute to the pathogenesis of gastric cancer.
表观遗传改变,如组蛋白修饰酶的异常表达,与肿瘤发生有关。Jumonji 结构域包含 2B(JMJD2B)是一种新鉴定的组蛋白去甲基酶,通过从组蛋白 H3 上的三甲基赖氨酸 9 上去除甲基残基来调节染色质结构或基因表达。最近的观察表明 JMJD2B 具有致癌活性。我们探讨了 JMJD2B 在癌细胞增殖、存活和肿瘤发生中的功能作用,并确定了其在胃癌中的表达谱。通过小干扰 RNA(siRNA)敲低胃癌和其他癌细胞中的 JMJD2B 表达,抑制了细胞增殖和/或诱导了细胞凋亡,并上调了 p53 和 p21(CIP1)蛋白的表达。增强的 p53 表达源于 DNA 损伤反应途径的激活。JMJD2B 敲低显著抑制了体内小鼠异种移植肿瘤的生长。此外,JMJD2B 在人类原发性胃癌组织中的表达增加。因此,JMJD2B 是体外和体内肿瘤细胞持续增殖和存活所必需的,其异常表达可能有助于胃癌的发病机制。