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Loss of miR-200c up-regulates CYP1B1 and confers docetaxel resistance in renal cell carcinoma.

Authors
 Inik Chang  ;  Yozo Mitsui  ;  Shinichiro Fukuhara  ;  Ankurpreet Gill  ;  Darryn K. Wong  ;  Soichiro Yamamura  ;  Varahram Shahryari  ;  Z. Laura Tabatabai  ;  Rajvir Dahiya  ;  Dong Min Shin  ;  Yuichiro Tanaka 
Citation
 ONCOTARGET , Vol.6(10) : 7774-7787, 2015 
Journal Title
 ONCOTARGET 
Issue Date
2015
MeSH
Aged ; Antineoplastic Agents/pharmacology ; Carcinoma, Renal Cell/drug therapy* ; Carcinoma, Renal Cell/genetics* ; Carcinoma, Renal Cell/pathology ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Cell Proliferation/genetics ; Cytochrome P-450 CYP1B1/genetics ; Cytochrome P-450 CYP1B1/metabolism* ; Drug Resistance, Neoplasm ; Female ; Humans ; Kidney Neoplasms/drug therapy* ; Kidney Neoplasms/genetics* ; Kidney Neoplasms/pathology ; Male ; MicroRNAs/genetics* ; MicroRNAs/metabolism ; Middle Aged ; Taxoids/pharmacology* ; Up-Regulation
Keywords
CYP1B1 ; chemotherapy ; docetaxel ; miR-200c ; renal cell carcinoma
Abstract
Despite high protein expression and enzymatic activity of cytochrome P450 1B1 (CYP1B1) in renal cell cancer (RCC), its functional significance has not been elucidated. Here we explored the functional role and regulatory mechanism of CYP1B1 in RCC. Reduction of CYP1B1 levels fail to prevent in vitro tumorigenicity such as proliferation, apoptosis, and cell cycle progression of RCC cells. Moreover, the expression levels are not associated with tumor type, stage, Fuhrman grade and 5-year survival probability after surgery. Instead, alteration of CYP1B1 expression regulates the chemosensitivity of RCC cells to docetaxel suggesting its critical contribution to the chemoresistance. Additionally, miR-200c, which is significantly down-regulated in RCC regulates CYP1B1 expression and activity. An inverse association was also observed between the expression levels of miR-200c and CYP1B1 protein in RCC tissues. Finally, alteration of miR-200c levels affects the chemosensitivity of RCC cells. Restoration of docetaxel resistance by exogenous expression of CYP1B1 in miR-200c-over-expressing cells indicates that CYP1B1 is a functional target of miR-200c. These results suggest that CYP1B1 up-regulation mediated by low miR-200c is one of the mechanisms underlying resistance of RCC cells to docetaxel. Therefore, expression of CYP1B1 and miR-200c in RCC may be useful as a prediction for docetaxel response.
Files in This Item:
T201501141.pdf Download
DOI
10.18632/oncotarget.3484
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
Yonsei Authors
Shin, Dong Min(신동민) ORCID logo https://orcid.org/0000-0001-6042-0435
Chang, In Ik(장인익)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/139953
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