Histone demethylase JMJD2B is required for tumor cell proliferation and survival and is overexpressed in gastric cancer

被引:64
|
作者
Li, Wenjuan [3 ]
Zhao, Li [3 ]
Zang, Wen [3 ]
Liu, Zhifang [3 ]
Chen, Long [3 ]
Liu, Tiantian [3 ]
Xu, Dawei [1 ,2 ,3 ]
Jia, Jihui [3 ]
机构
[1] Karolinska Univ Hosp, Div Hematol, Dept Med, Solna, Sweden
[2] Karolinska Inst, Stockholm, Sweden
[3] Shandong Univ, Sch Med, Dept Microbiol, Key Lab Expt Teratol,Chinese Minist Educ, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
Epigenetics; Histone demethylase; JMJD2B; Gastric cancer; Tumorigenesis; TELOMERASE REVERSE-TRANSCRIPTASE; DNA-DAMAGE RESPONSE; CARCINOGENESIS; GENE; TRIMETHYLATION; METHYLATION; SENESCENCE; REPRESSION; HYPOXIA; FAMILY;
D O I
10.1016/j.bbrc.2011.11.045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:372 / 378
页数:7
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