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MicroRNA‐195 Chemosensitizes Colon Cancer Cells to the Chemotherapeutic Drug Doxorubicin by Targeting the First Binding Site of BCL2L2 mRNA
Author(s) -
Qu Juan,
Zhao Liang,
Zhang Pengzhi,
Wang Juan,
Xu Ning,
Mi Wenjuan,
Jiang Xingwang,
Zhang Changming,
Qu Juan
Publication year - 2015
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.24366
Subject(s) - microrna , gene knockdown , apoptosis , doxorubicin , cancer research , cell culture , biology , cancer cell , microbiology and biotechnology , carcinogenesis , cytotoxicity , viability assay , transfection , cell , chemistry , cancer , in vitro , biochemistry , chemotherapy , gene , genetics
The mechanisms underlying doxorubicin (Dox) resistance in colon cancer cells are not fully understood. MicroRNA (miRNA) play important roles in tumorigenesis and drug resistance. However, the relationship between miRNA and Dox resistance in colon cancer cells has not been previously explored. In this study, we utilized microRNA array and real‐time PCR to verify that miR‐127, miR‐195, miR‐22, miR‐137 were significantly down‐regulated, while miR‐21, miR‐592 were up‐regulated in both HT29/DOX and LOVO/DOX cell lines. In vitro cell viability assay showed that knockdown of miR‐195 in HT29 and LOVO cells caused a marked inhibition of Dox‐induced cytotoxicity. Moreover, we explored that miR‐195 is involved in repression of BCL2L2 expression through targeting its 3′‐untranslated region, especially the first binding site within its mRNA. Furthermore, down‐regulation of miR‐195 conferred DOX resistance in parental cells and reduced cell apoptosis activity, while over‐expression of miR‐195 sensitized resistant cells to DOX and enhanced cell apoptosis activity, all of which can be partly rescued by BCL2L2 siRNA and cDNA expression. These results may have implications for therapeutic strategies aiming to overcome colon cancer cell resistance to Dox. J. Cell. Physiol. 230: 535–545, 2015. © 2014 Wiley Periodicals, Inc., A Wiley Company