MiR-128 inhibits tumor growth and angiogenesis by targeting p70S6K1

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. O...

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Veröffentlicht in:PloS one 2012-03, Vol.7 (3), p.e32709-e32709
Hauptverfasser: Shi, Zhu-mei, Wang, Jing, Yan, Zhiping, You, Yong-ping, Li, Chong-yong, Qian, Xu, Yin, Yu, Zhao, Peng, Wang, Ying-ying, Wang, Xie-feng, Li, Ming-na, Liu, Ling-Zhi, Liu, Ning, Jiang, Bing-Hua
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Sprache:eng
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Zusammenfassung: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.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0032709