MiRNA-101 inhibits breast cancer growth and metastasis by targeting CX chemokine receptor 7 |
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Authors: | Jun-Tang Li Lin-Tao Jia Ning-Ning Liu Xiao-Shan Zhu Qin-Qin Liu Xiu-Li Wang Feng Yu Yan-Li Liu An-Gang Yang Chun-Fang Gao |
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Affiliation: | 1. Centre of Inflammation and Cancer Research, 150th Central Hospital of PLA, Luoyang, Henan 471031, China;2. State Key Laboratory of Cancer Biology, Department of Immunology, Fourth Military Medical University, Xi''an, Shaanxi 710032, China;3. State Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi''an, Shaanxi 710032, China |
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Abstract: | ![]() 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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Keywords: | breast cancer MiR-101 CXCR7 proliferation metastasis |
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