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微小RNA-101通过靶向CXC趋化因子受体7抑制乳腺癌的生长和转移。

MiRNA-101 inhibits breast cancer growth and metastasis by targeting CX chemokine receptor 7.

作者信息

Li Jun-Tang, Jia Lin-Tao, Liu Ning-Ning, Zhu Xiao-Shan, Liu Qin-Qin, Wang Xiu-Li, Yu Feng, Liu Yan-Li, Yang An-Gang, Gao Chun-Fang

机构信息

Centre of Inflammation and Cancer Research, 150th Central Hospital of PLA, Luoyang, Henan 471031, China.

State Key Laboratory of Cancer Biology, Department of Immunology, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.

出版信息

Oncotarget. 2015 Oct 13;6(31):30818-30. doi: 10.18632/oncotarget.5067.

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.

摘要

虽然miR-101参与乳腺癌的发生和发展,但其潜在的分子机制仍有待阐明。在此,我们报道miR-101的表达与乳腺癌的临床分期、淋巴结转移及预后呈负相关。导入miR-101可在体外抑制乳腺癌细胞的增殖和侵袭,并在体内抑制肿瘤生长和肺转移。CXC趋化因子受体7(CXCR7)是miR-101的直接靶点,与乳腺癌患者的组织学分级和淋巴结转移发生率呈正相关。分别通过CXCR7基因敲除和过表达模拟并抵消了miR-101的作用。CXCR7下游的STAT3信号传导参与miR-101对乳腺癌细胞行为的调控。这些发现为miR-101在乳腺癌治疗中的潜在应用提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae1/4741570/65a946d0cc23/oncotarget-06-30818-g001.jpg

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