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硫氧还蛋白在仓鼠和人胆管癌进展过程中的表达。

Expression of thioredoxin during progression of hamster and human cholangiocarcinoma.

机构信息

School of Veterinary Medicine and Institute of Veterinary Science, Kangwon National University, Chuncheon, Korea.

出版信息

Cancer Sci. 2010 Jan;101(1):281-8. doi: 10.1111/j.1349-7006.2009.01353.x. Epub 2009 Sep 8.

Abstract

Thioredoxin (Trx) is a multifunctional redox protein that has growth-promoting and anti-apoptotic effects on cells and protects cells from endogenous and exogenous free radicals. Recently, altered expression of Trx has been reported in various cancers. In the present study, we investigated altered expression of Trx at the precancerous and carcinogenic phases during cholangiocarcinogenesis in a hamster cholangiocarcinoma (ChC) model, using semiquantitative immunohistochemical and Western blot analyses. Moreover, to determine if the results correlated well with those in human ChCs, we carried out a comparative immunohistochemical study for Trx in tissue-arrayed human ChCs with different grades of tumor cell differentiation. Trx was found highly expressed in the cytoplasm of dysplastic bile ducts with highly abnormal growth patterns and ChCs irrespective of tumor type or tumor cell differentiation. Overexpression of Trx at the precancerous and carcinogenic phases was further supported by significant elevation of Trx protein in Western blotting. The results from the hamster ChCs were in good agreement with those from human ChCs. Our results strongly suggested that the redox regulatory function of Trx plays an important role in bile duct cell transformation and tumor progression during cholangiocarcinogenesis.

摘要

硫氧还蛋白(Trx)是一种多功能的氧化还原蛋白,对细胞具有促进生长和抗凋亡作用,并能保护细胞免受内源性和外源性自由基的伤害。最近,有研究报道 Trx 的表达在各种癌症中发生改变。本研究采用半定量免疫组化和 Western blot 分析,在仓鼠胆管癌(ChC)模型的癌前和致癌阶段,研究了 Trx 的改变表达。此外,为了确定这些结果是否与人胆管癌的结果相符,我们对不同肿瘤细胞分化程度的组织排列的人胆管癌中的 Trx 进行了比较免疫组化研究。结果发现,在具有高度异常生长模式的发育不良胆管和 ChC 中,Trx 高度表达于细胞质中,而与肿瘤类型或肿瘤细胞分化无关。Western blot 分析显示 Trx 蛋白水平显著升高,进一步支持了癌前和致癌阶段 Trx 的过表达。仓鼠 ChC 的结果与人 ChC 的结果非常一致。我们的结果强烈表明,Trx 的氧化还原调节功能在胆管细胞转化和胆管癌发生过程中的肿瘤进展中发挥重要作用。

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