Direct Upregulation of STAT3 by MicroRNA-551b-3p Deregulates Growth and Metastasis of Ovarian Cancer
Author(s) -
Pradeep ChaluvallyRaghavan,
Kang Jin Jeong,
Sunila Pradeep,
Andreia Silva,
Shuangxing Yu,
Wenbin Liu,
Tyler Moss,
Cristian RodriguezAguayo,
Dong Zhang,
Prahlad T. Ram,
Jinsong Liu,
Yiling Lu,
Gabriel López-Berestein,
George A. Călin,
Anil K. Sood,
Gordon B. Mills
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.04.034
Subject(s) - ovarian cancer , stat3 , cancer research , downregulation and upregulation , microrna , biology , metastasis , in vivo , transcription factor , cell growth , cancer cell , cancer , apoptosis , gene , genetics
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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