miR-125b is methylated and functions as a tumor suppressor by regulating the ETS1 proto-oncogene in human invasive breast cancer.

نویسندگان

  • Yan Zhang
  • Li-Xu Yan
  • Qi-Nian Wu
  • Zi-Ming Du
  • Jing Chen
  • Ding-Zhun Liao
  • Ma-Yan Huang
  • Jing-Hui Hou
  • Qiu-Liang Wu
  • Mu-Sheng Zeng
  • Wen-Lin Huang
  • Yi-Xin Zeng
  • Jian-Yong Shao
چکیده

The microRNA miR-125b is dysregulated in various human cancers but its underlying mechanisms of action are poorly understood. Here, we report that miR-125b is downregulated in invasive breast cancers where it predicts poor patient survival. Hypermethylation of the miR-125b promoter partially accounted for reduction of miR-125b expression in human breast cancer. Ectopic restoration of miR-125b expression in breast cancer cells suppressed proliferation, induced G(1) cell-cycle arrest in vitro, and inhibited tumorigenesis in vivo. We identified the ETS1 gene as a novel direct target of miR-125b. siRNA-mediated ETS1 knockdown phenocopied the effect of miR-125b in breast cell lines and ETS1 overexpression in invasive breast cancer tissues also correlated with poor patient prognosis. Taken together, our findings point to an important role for miR-125b in the molecular etiology of invasive breast cancer, and they suggest miR-125b as a potential theranostic tool in this disease.

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Molecular and Cellular Pathobiology miR-125b Is Methylated and Functions as a Tumor Suppressor by Regulating the ETS1 Proto-oncogene in Human Invasive Breast Cancer

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عنوان ژورنال:
  • Cancer research

دوره 71 10  شماره 

صفحات  -

تاریخ انتشار 2011