Choi Joon Hyuk, Kim Tae Nyeun, Kim Seongyong, Baek Suk-Hwan, Kim Jung Hye, Lee Seung Rock, Kim Jae-Ryong
Department of Pathology, College of Medicine, Yeungnam University, Daegu, 705-717, Korea.
Anticancer Res. 2002 Nov-Dec;22(6A):3331-5.
Thioredoxin reductase 2 (TrxR2), thioredoxin II (Trx II) and peroxiredoxin III (Prx III) are specifically localized in mitochondria and believed to play important roles in the regulation of cellular redox status by serving as a primary line of defense against H2O2 produced during respiration. Substantial evidence indicates that the alteration of cellular redox status is a critical factor involved in cell growth and death and results in tumorigenesis. We therefore investigated the expression of TrxR2 and Prx III in 58 paraffin-embedded hepatocellular carcinoma tissues by immunohistochemistry. The labeling indices of TrxR2 and Prx III were significantly higher in tumor tissues than in the corresponding adjacent normal tissues. In 39 (67.2%) out of 58 samples, the levels of TrxR2 expression were higher in tumor tissues than in corresponding adjacent normal tissues, while 11 samples (19.0%) showed lower expression in tumor tissues. Prx III expression was increased in tumor tissues of 23 samples (39.7%) compared to adjacent normal tissues and were decreased in 18 samples (31.0%). These results suggest that alterations in cellular redox status by enhanced expression of TrxR2 and/or Prx III might be associated with the formation and development of hepatocellular carcinomas.
硫氧还蛋白还原酶2(TrxR2)、硫氧还蛋白II(Trx II)和过氧化物氧还蛋白III(Prx III)特异性定位于线粒体,并且被认为通过作为抵御呼吸过程中产生的过氧化氢的第一道防线,在调节细胞氧化还原状态中发挥重要作用。大量证据表明,细胞氧化还原状态的改变是参与细胞生长和死亡的关键因素,并导致肿瘤发生。因此,我们通过免疫组织化学研究了58例石蜡包埋的肝细胞癌组织中TrxR2和Prx III的表达。TrxR2和Prx III的标记指数在肿瘤组织中显著高于相应的癌旁正常组织。在58个样本中的39个(67.2%)中,肿瘤组织中TrxR2的表达水平高于相应的癌旁正常组织,而11个样本(19.0%)在肿瘤组织中表达较低。与癌旁正常组织相比,23个样本(39.7%)的肿瘤组织中Prx III表达增加,18个样本(31.0%)中Prx III表达降低。这些结果表明,TrxR2和/或Prx III表达增强引起的细胞氧化还原状态改变可能与肝细胞癌的形成和发展有关。