Abstract |
BACKGROUND Ezrin- radixin- moesin (ERM) plays an important role in multiple links of tumors. It also involved in breast cancer invasion and metastasis, and might be a potential biomarker of breast cancer. Another study suggested that ERM expression was regulated directly by miR-200c, and had a critical role in miR-200c suppressing cell migration. This study aimed to investigate the effect of miR-200b on ERM expression in a breast cancer cell line and its influence on invasion and metastasis ability in vitro. MATERIAL AND METHODS Breast cancer cell lines MCF-7 and MDA-MB-231 with different metastatic potentials were selected as a model. MiR-200b overexpression or inhibition was achieved by Lipofectamine™ 2000-mediated miRNA transfection. RT-PCR was used to test miR-200b level, while Western blot was selected to detect ERM protein expression. Wound healing assay and Transwell assay were performed to determine cell migration and invasion ability. RESULTS RT-PCR revealed that miR-200b level in MDA-MB-231 was obviously lower than that in MCF-7, while Western blot analysis showed that ERM expression was significantly higher. MiR-200b inhibition by transfection in MCF-7 markedly decreased miR-200b level, elevated ERM expression, and enhanced cell migration and invasion. MiR-200b overexpression in MDA-MB-231 obviously increased miR-200b level, reduced ERM expression, and weakened cell migration and invasion. CONCLUSIONS MiR-200b participates in breast cancer cell migration and invasion through regulating ERM in MCF-7 and MDA-MB-231.
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Authors | Hong Hong, Haizhong Yu, Jianfen Yuan, Chunyan Guo, Hongyan Cao, Weibing Li, Chunhong Xiao |
Journal | Medical science monitor : international medical journal of experimental and clinical research
(Med Sci Monit)
Vol. 22
Pg. 1946-52
(Jun 08 2016)
ISSN: 1643-3750 [Electronic] United States |
PMID | 27276064
(Publication Type: Journal Article)
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Chemical References |
- DNA-Binding Proteins
- ETV5 protein, human
- MIRN200 microRNA, human
- MicroRNAs
- Transcription Factors
- Amlodipine
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Topics |
- Amlodipine
(metabolism)
- Breast Neoplasms
(genetics, metabolism, pathology)
- Cell Line, Tumor
- Cell Movement
(genetics)
- Cell Proliferation
(genetics)
- DNA-Binding Proteins
(biosynthesis, genetics, metabolism)
- Female
- Humans
- MCF-7 Cells
- MicroRNAs
(administration & dosage, biosynthesis, genetics, metabolism)
- Neoplasm Invasiveness
- Transcription Factors
(biosynthesis, genetics, metabolism)
- Transfection
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