MiRNA-101 inhibits breast cancer growth and metastasis by targeting CX chemokine receptor 7
Author(s) -
Juntang Li,
Lintao Jia,
Ningning Liu,
Xiaoshan Zhu,
Qinqin Liu,
Xiuli Wang,
Feng Yu,
Yanli Liu,
Angang Yang,
Chunfang Gao
Publication year - 2015
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.5067
Subject(s) - breast cancer , cancer research , metastasis , medicine , chemokine receptor , lung cancer , chemokine , cancer , microrna , cell growth , oncology , receptor , biology , biochemistry , genetics , gene
Whereas miR-101 is involved in the development and progression of breast cancer, the underlying molecular mechanisms remain to be elucidated. Here, we report that miR-101 expression is inversely correlated with the clinical stage, lymph node metastasis and prognosis in breast cancers. Introduction of miR-101 inhibited breast cancer cell proliferation and invasion in vitro and suppressed tumor growth and lung metastasis of in vivo. CX chemokine receptor 7 (CXCR7) is a direct target of miR-101, positively correlating with the histological grade and the incidence of lymph node metastasis in breast cancer patients. The effects of miR-101 were mimicked and counteracted by CXCR7 depletion and overexpression, respectively. STAT3 signaling downstream of CXCR7 is involved in miR-101 regulation of breast cancer cell behaviors. These findings have implications for the potential application of miR-101 in breast cancer treatment.
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