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miR-671-5p Inhibits Tumor Proliferation by Blocking Cell Cycle in Osteosarcoma
被引:45
作者:
Xin, Chaofei
[1
]
Lu, Shitao
[1
]
Li, Yu
[1
]
Zhang, Yi
[1
]
Tian, Jinxiang
[1
]
Zhang, Shaokun
[1
]
Yang, Shangliang
[1
]
Gao, Tianhao
[1
]
Xu, Jianzhong
[1
]
机构:
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Orthoped Surg, Zhengzhou 450000, Henan, Peoples R China
基金:
中国国家自然科学基金;
关键词:
miR-671-5p;
proliferation;
cell cycle;
osteosarcoma;
CCND1;
CDC34;
TARGETING MICRORNAS;
PROMOTES;
EXPRESSION;
CANCER;
D O I:
10.1089/dna.2019.4870
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:
Osteosarcoma (OS), a highly aggressive bone tumor, mainly occurs in young patients and always presents abnormalities in molecular biology, such as microRNAs (miRNAs). However, the characteristic and underlying mechanism of miR-671-5p in OS are still unclear. In this study, we certify that miR-671-5p is remarkably downregulated in OS tissues and cells. Overexpressed miR-671-5p can suppress OS cell proliferation in vivo and in vitro, by the way of arresting cell-cycle progression. The overexpression of cyclin D1 (CCND1) and CDC34 promotes cell proliferation and cell-cycle promotion, whose functions are contrary to miR-671-5p. miR-671-5p directly binds to CCND1 and CDC34, which are thought as the key factors in regulating cell cycle. Taken together, our results suggest that by targeting CCND1 and CDC34, miR-671-5p plays a tumor suppressor in OS to inhibit the development of OS, implicating it as a novel target for therapeutic intervention in OS.
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页码:996 / 1004
页数:9
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