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MiRNA-101 inhibits breast cancer growth and metastasis by targeting CX chemokine receptor 7.
- Source :
-
Oncotarget [Oncotarget] 2015 Oct 13; Vol. 6 (31), pp. 30818-30. - Publication Year :
- 2015
-
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.
- Subjects :
- Animals
Apoptosis
Breast Neoplasms genetics
Breast Neoplasms mortality
Breast Neoplasms pathology
Breast Neoplasms surgery
Cell Line, Tumor
Female
Gene Expression Regulation, Neoplastic
HEK293 Cells
Humans
Kaplan-Meier Estimate
Lung Neoplasms genetics
Lung Neoplasms mortality
Lung Neoplasms prevention & control
Lung Neoplasms secondary
Lymphatic Metastasis
Mice, Inbred BALB C
MicroRNAs genetics
Neoplasm Grading
Neoplasm Invasiveness
RNA Interference
Receptors, CXCR genetics
STAT3 Transcription Factor metabolism
Signal Transduction
Time Factors
Transfection
Tumor Burden
Breast Neoplasms metabolism
Cell Movement
Cell Proliferation
Lung Neoplasms metabolism
MicroRNAs metabolism
Receptors, CXCR metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1949-2553
- Volume :
- 6
- Issue :
- 31
- Database :
- MEDLINE
- Journal :
- Oncotarget
- Publication Type :
- Academic Journal
- Accession number :
- 26360780
- Full Text :
- https://doi.org/10.18632/oncotarget.5067