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DNA Cell Biol. 2014 May;33(5):291-300. doi: 10.1089/dna.2013.2132. Epub 2014 Mar 31.

microRNA-200a inhibits cell proliferation by targeting mitochondrial transcription factor A in breast cancer.

Author information

1
1 Department of General Surgery, The Second Xiangya Hospital of Central South University , Changsha, China .

Abstract

microRNAs (miRNAs) are endogenous 19-25 nucleotide noncoding single-stranded RNAs that regulate gene expression by blocking the translation or decreasing the stability of mRNAs. In this study, we showed that miR-200a expression levels were decreased while mitochondrial transcription factor A (TFAM) mRNA expression levels were increased in breast cancer (BC) tissues and cell lines, and identified TFAM as a novel direct target of miR-200a. Overexpression of miR-200a suppressed TFAM protein expression, mtDNA copy number, and attenuated cell proliferation. Forced expression of TFAM can partly rescue the inhibitory effect of miR-200a in the cells. Taken together, these findings will shed light on the role and mechanism of miR-200a in regulating BC cells growth and mtDNA copy number via miR-200a/TFAM axis, and miR-200a may serve as a potential therapeutic target in BC in the future.

PMID:
24684598
DOI:
10.1089/dna.2013.2132
[Indexed for MEDLINE]

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