MiR-128 Inhibits Tumor Growth and Angiogenesis by Targeting p70S6K1

被引:104
|
作者
Shi, Zhu-mei [1 ]
Wang, Jing [2 ]
Yan, Zhiping [2 ]
You, Yong-ping [1 ]
Li, Chong-yong [2 ]
Qian, Xu [2 ]
Yin, Yu [2 ]
Zhao, Peng [1 ]
Wang, Ying-ying [1 ]
Wang, Xie-feng [1 ]
Li, Ming-na [3 ]
Liu, Ling-Zhi [4 ]
Liu, Ning [1 ]
Jiang, Bing-Hua [1 ,2 ,4 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Neurosurg, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Pathol, Ctr Canc, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Pathol, Nanjing, Jiangsu, Peoples R China
[4] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
来源
PLOS ONE | 2012年 / 7卷 / 03期
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
CANCER CELLS; MICRORNAS; EXPRESSION; ACTIVATION; GLIOBLASTOMA; PATHWAY; VEGF; AKT; PCR; TUMORIGENESIS;
D O I
10.1371/journal.pone.0032709
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs are a class of small noncoding RNAs that function as critical gene regulators through targeting mRNAs for translational repression or degradation. In this study, we showed that miR-128 expression levels were decreased in glioma, and identified p70S6K1 as a novel direct target of miR-128. Overexpression of miR-128 suppressed p70S6K1 and its downstream signaling molecules such as HIF-1 and VEGF expression, and attenuated cell proliferation, tumor growth and angiogenesis. Forced expression of p70S6K1 can partly rescue the inhibitory effect of miR-128 in the cells. Taken together, these findings will shed light to the role and mechanism of miR-128 in regulating glioma tumor angiogenesis via miR-128/p70S6K1 axis, and miR-128 may serve as a potential therapeutic target in glioma in the future.
引用
收藏
页数:10
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