Abstract
miR-128 is more highly expressed in drug-resistant breast cancer samples than in drug-sensitive samples. We have confirmed that Bax is the target of miR-128 by negative post-transcriptional regulation. miR-128 and Bax were detected in the breast cancer cell line, MDA-MB-231, which was then transfected with miR-128 MIMIC (precursor of miR-128) or AMO (antisense-miR-128 oligonucleotides). After transfection, the chemosensitivity of MDA-MB-231 cell was up-regulated with increasing of Bax and inhibition of miR-128.
© 2013 International Federation for Cell Biology.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Apoptosis
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Breast Neoplasms / metabolism
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Breast Neoplasms / pathology
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Cell Line, Tumor
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Down-Regulation
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Drug Resistance, Neoplasm
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Female
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Humans
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MicroRNAs / antagonists & inhibitors
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MicroRNAs / metabolism*
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Middle Aged
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Oligonucleotides, Antisense / metabolism
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RNA Interference
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RNA, Small Interfering / metabolism
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bcl-2-Associated X Protein / antagonists & inhibitors
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bcl-2-Associated X Protein / genetics
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bcl-2-Associated X Protein / metabolism*
Substances
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MIRN128 microRNA, human
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MicroRNAs
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Oligonucleotides, Antisense
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RNA, Small Interfering
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bcl-2-Associated X Protein