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Diethylnitrosamine으로 유도된 쥐의 간암화 과정에서 세포주기및 세포자멸사 관련 단백 발현Expression of Proteins Related Cell Cycle and Apoptosis during Diethylnitrosamine (DEN)-induced Hepatocarcinogenesis in Rats

Authors
심우정김용석최유신김범규차성재임현묵박언섭
Issue Date
2008
Publisher
대한외과학회
Keywords
세포주기 관련 단백질; 세포자멸사 관련 단백질; Diethylnitrosamine; Cell cycle-related protein; Apoptosis-related protein
Citation
대한외과학회지, v.75, no.6, pp 359 - 367
Pages
9
Journal Title
대한외과학회지
Volume
75
Number
6
Start Page
359
End Page
367
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/31703
ISSN
2288-6575
2288--679
Abstract
Purpose: To explore the role of cell cycle and apoptosis regulators during hepatocarcinogenesis, the expression of cell cycle-related proteins (cyclin D1 and p27kip1) and apoptosis-related proteins (p53, survivin, caspase 3). Methods: Sprague-Dawley rats were given 120 ppm diethylnitrosamine (DEN) as a carcinogen and sequentially sacrificed. The expression of cell cycle and apoptotic related proteins were examined by light microscopy and immunohistochemistry. Results: During the DEN-induced hepatocarcinogenesis, sequential histologic changes from preneoplastic lesions (altered hepatic cellular foci, hyperplastic nodules, and hepatocellular adenomas) and ultimately overt hepatocellular carcinomas and metastatic lesions were noted. The cyclin D1 were progressively increased from preneoplastic lesions to hepatocellular carcinomas. However, the p27kip1 and the survivine proteins did not show any other difference with the increasing degree of carcinogenesis. The p53 and caspase 3 proteins were more significantly increased in hepatocellular carcinomas than preneoplastic lesions. The cyclin D1 protein expression did not show any correlation with the expression of p27Kip1 protein, but the p53 expression was related to the expression of survivin and caspase 3. Conclusion: From the above results, over-expression of cyclin D1 plays a role in the early and late stages of hepatocarcinogenesis. In addition p53 and caspase 3 might be useful markers for evaluating the risk of malignant transformation. (J Korean Surg Soc 2008;75:359-367)
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