PTEN公司
癌症研究
自噬
程序性细胞死亡
细胞生长
蛋白激酶B
癌基因
小RNA
细胞凋亡
生物
癌症
细胞生物学
PI3K/AKT/mTOR通路
细胞
信号转导
细胞周期
遗传学
基因
作者
Huijun Wei,Ri Cui,Julian Bahr,Nicola Zanesi,Zhenghua Luo,Wei Meng,Guang Liang,Carlo M. Croce
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2017-09-22
卷期号:77 (22): 6168-6178
被引量:57
标识
DOI:10.1158/0008-5472.can-17-0530
摘要
Abstract H-RasV12 oncogene has been shown to promote autophagic cell death. Here, we provide evidence of a contextual role for H-RasV12 in cell death that is varied by its effects on miR-130a. In E1A-immortalized murine embryo fibroblasts, acute expression of H-RasV12 promoted apoptosis, but not autophagic cell death. miRNA screens in this system showed that miR-130a was strongly downregulated by H-RasV12 in this model system. Enforced expression of miR-130a increased cell proliferation in part via repression of PTEN. Consistent with this effect, miR-130a overexpression in human breast cancer cells promoted Akt phosphorylation, cell survival, and tumor growth. In clinical specimens of multiple human cancers, expression of miR-130 family members correlated inversely with PTEN expression. Overall, our results defined miR-130a as an oncogenic miRNA that targets PTEN to drive malignant cell survival and tumor growth. Cancer Res; 77(22); 6168–78. ©2017 AACR.
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