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硫氧还蛋白对细胞生长和死亡的氧化还原调控以及抑制剂的作用。

Thioredoxin redox control of cell growth and death and the effects of inhibitors.

作者信息

Powis G, Kirkpatrick D L, Angulo M, Baker A

机构信息

Arizona Cancer Center, University of Arizona, Tucson 85724-5024, USA.

出版信息

Chem Biol Interact. 1998 Apr 24;111-112:23-34. doi: 10.1016/s0009-2797(97)00148-8.

Abstract

Thioredoxin is a redox protein found over-expressed in some human tumors. Thioredoxin is secreted by tumor cells and stimulates cancer cell growth. Redox activity is essential for growth stimulation by thioredoxin. Cells transfected with thioredoxin cDNA show increased tumor growth and decreased apoptosis in vivo and decreased sensitivity to apoptosis induced by a variety of agents both in vitro and in vivo. Cells transfected with a redox-inactive mutant thioredoxin show inhibited tumor growth in vivo. Thus, thioredoxin offers an attractive target for anticancer drug development. A class of disulfide inhibitors of thioredoxin has been identified. These disulfides inhibit cancer cell growth in culture and have antitumor activity against some human tumor xenografts in animals.

摘要

硫氧还蛋白是一种在某些人类肿瘤中过度表达的氧化还原蛋白。硫氧还蛋白由肿瘤细胞分泌,并刺激癌细胞生长。氧化还原活性对于硫氧还蛋白的生长刺激作用至关重要。用硫氧还蛋白cDNA转染的细胞在体内显示出肿瘤生长增加和凋亡减少,并且在体外和体内对多种诱导剂诱导的凋亡敏感性降低。用氧化还原无活性的突变型硫氧还蛋白转染的细胞在体内显示出肿瘤生长受到抑制。因此,硫氧还蛋白为抗癌药物开发提供了一个有吸引力的靶点。已鉴定出一类硫氧还蛋白的二硫键抑制剂。这些二硫键在培养中抑制癌细胞生长,并对动物体内的一些人类肿瘤异种移植具有抗肿瘤活性。

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