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자료유형
학술저널
저자정보
Kwon, Yeo-Jung (College of Pharmacy, Chung-Ang University) Jung, Jin-Joo (College of Pharmacy, Chung-Ang University) Park, Na-Hee (College of Pharmacy, Chung-Ang University) Ye, Dong-Jin (College of Pharmacy, Chung-Ang University) Kim, Donghak (Department of Biological Sciences, Konkuk University) Moon, Aree (College of Pharmacy, Duksung Women's University) Chun, Young-Jin (College of Pharmacy, Chung-Ang University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제21권 제3호
발행연도
2013.1
수록면
190 - 195 (6page)

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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. Over-expression 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.

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