Functional elucidation of MiR-34 in osteosarcoma cells and primary tumor samples

被引:204
作者
He, Chunlei [2 ]
Xiong, Jianyi [1 ]
Xu, Xiaoping [1 ]
Lu, Wei [1 ]
Liu, Lijun [1 ]
Xiao, Deming [1 ]
Wang, Daping [1 ]
机构
[1] Shenzhen Second Peoples Hosp, Dept Traumat Orthopead, Shenzhen 518035, Guangdong, Peoples R China
[2] Guangzhou Med Coll, Guangzhou 510182, Guangdong, Peoples R China
关键词
MiR-34; p53; Osteosarcoma; MICRORNA EXPRESSION; HUMAN CANCERS; P53; APOPTOSIS; MECHANISMS; SUPPRESSOR; ACTIVATION; TARGETS; NETWORK; GENES;
D O I
10.1016/j.bbrc.2009.07.101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
MiR-34s have been characterized as direct p53 targets, which induce apoptosis, cell cycle arrest, and senescence. MiR-34s were found to associate with tumorigenesis. Thus far, there is no study on the role of MiR-34s in osteosarcoma. In the current study, we intensively investigated the function of MiR-34s in two osteosarcoma cell lines: U2OS (p53(+/+)) and SAOS-2 (p53 (/) ). We found that MiR-34s affect the expression of its target genes partially in a p53-dependent manner. And p53 also partially contributes to the MiR-34s induced cell cycle arrest and apoptosis. Finally, we examined the expression, genetic and epigenetic alterations of MiR-34 gene in 117 primary osteosarcoma samples. Expression of MiR-34s was decreased in tumor samples, and MiR-34 genes underwent minimal deletions and epigenetic inactivation in osteosarcomas. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 40
页数:6
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