卵巢癌
车站3
癌症研究
下调和上调
小RNA
生物
转移
体内
转录因子
细胞生长
癌细胞
癌症
细胞凋亡
基因
遗传学
作者
Pradeep Chaluvally‐Raghavan,Kang Jin Jeong,Sunila Pradeep,Andreia Silva,Shuangxing Yu,Wenbin Liu,Tyler Moss,Cristian Rodriguez‐Aguayo,Dong Zhang,Prahlad T. Ram,Jinsong Liu,Yiling Lu,Gabriel Lopez‐Berestein,George A. Călin,Anil K. Sood,Gordon B. Mills
出处
期刊:Cell Reports
[Cell Press]
日期:2016-05-01
卷期号:15 (7): 1493-1504
被引量:85
标识
DOI:10.1016/j.celrep.2016.04.034
摘要
3q26.2 amplification in high-grade serous ovarian cancer leads to increased expression of mature microRNA miR551b-3p, which is associated with poor clinical outcome. Importantly, miR551b-3p contributes to resistance to apoptosis and increased survival and proliferation of cancer cells in vitro and in vivo. miR551b-3p upregulates STAT3 protein levels, and STAT3 is required for the effects of miR551b-3p on cell proliferation. Rather than decreasing levels of target mRNA as expected, we demonstrate that miR551b-3p binds a complementary sequence on the STAT3 promoter, recruiting RNA polymerase II and the TWIST1 transcription factor to activate STAT3 transcription, and thus directly upregulates STAT3 expression. Furthermore, anti-miR551b reduced STAT3 expression in ovarian cancer cells in vitro and in vivo and reduced ovarian cancer growth in vivo. Together, our data demonstrate a role for miR551b-3p in transcriptional activation. Thus, miR551b-3p represents a promising candidate biomarker and therapeutic target in ovarian cancer.
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