Annexin A5 as a New Potential Biomarker for Cisplatin-Induced Toxicity in Human Kidney Epithelial Cells

被引:14
|
作者
Kwon, Yeo-Jung [1 ]
Jung, Jin-Joo [1 ]
Park, Na-Hee [1 ]
Ye, Dong-Jin [1 ]
Kim, Donghak [2 ]
Moon, Aree [3 ]
Chun, Young-Jin [1 ]
机构
[1] Chung Ang Univ, Coll Pharm, Seoul 156756, South Korea
[2] Konkuk Univ, Dept Biol Sci, Seoul 143701, South Korea
[3] Duksung Womens Univ, Coll Pharm, Seoul 132714, South Korea
关键词
Cisplatin; Annexin A5; Nephrotoxicity; Biomarker; Proteomic analysis; EXPRESSION; APOPTOSIS; CALCIUM; PHOSPHATIDYLSERINE; NEPHROTOXICITY; CARBOPLATIN; PROTEINS; BINDING;
D O I
10.4062/biomolther.2013.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cisplatin is a member of platinum-containing anti-cancer drugs that causes cross-linking of DNA and ultimately cancer cell apoptosis. The therapeutic function of cisplatin on various types of cancers has been widely reported but the side effects have been discovered together and nephrotoxicity has been regarded as major side effect of cisplatin. To select candidates for new sensitive nephrotoxicity biomarker, we performed proteomic analysis using 2-DE/MALDI-TOF-MS followed by cisplatin treatment in human kidney cell line, HK-2 cells, and compared the results to the gene profile from microarray composed of genes changed in expression by cisplatin from formerly reported article. Annexin A5 has. been selected to be the most potential candidate and it has been identified using Western blot, RT-PCR and cell viability assay whether annexin A5 is available to be a sensitive nephrotoxic biomarker. Treatment with cisplatin on HK-2 cells caused the increase of annexin A5 expression in protein and mRNA levels. Overexpression of annexin A5 blocked HK-2 cell proliferation, indicating correlation between annexin A5 and renal cell toxicity. Taken together, these results suggest the possibility of annexin A5 as a new biomarker for cisplatin-mediated nephrotoxicity.
引用
收藏
页码:190 / 195
页数:6
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