Powis G, Oblong J E, Gasdaska P Y, Berggren M, Hill S R, Kirkpatrick D L
Arizona Cancer Center, Tucson 85724, USA.
Oncol Res. 1994;6(10-11):539-44.
Thioredoxin is a redox protein that is important for a variety of intracellular functions, possibly including regulation of transcription factor activity. We have shown that human thioredoxin has the same predicted amino acid sequence as adult T-cell-derived leukemic cell growth factor. Recombinant human thioredoxin stimulates the proliferation of Swiss murine 3T3 fibroblasts with an EC50 of 100 nM and the proliferation of a number of human cancer cells. Site-directed mutagenesis of the active-site cysteines of thioredoxin has shown that redox activity is necessary for the stimulation of cell proliferation. Added 125I-thioredoxin is taken up by cells in culture and could have intracellular action. A series of alkyl 2-imidazolyl disulfides have been shown to be competitive inhibitors of human thioredoxin reductase with Ki values of 3.3 to 8.6 microM. The compounds inhibited Swiss 3T3 serum-dependent proliferation with IC50 values of 2.0 to 4.0 microM, and one compound inhibited Swiss 3T3 thioredoxin-dependent proliferation with an IC50 value of 60 nM.
硫氧还蛋白是一种氧化还原蛋白,对多种细胞内功能至关重要,可能包括转录因子活性的调节。我们已经表明,人硫氧还蛋白与成人T细胞来源的白血病细胞生长因子具有相同的预测氨基酸序列。重组人硫氧还蛋白以100 nM的半数有效浓度(EC50)刺激瑞士小鼠3T3成纤维细胞的增殖以及多种人类癌细胞的增殖。硫氧还蛋白活性位点半胱氨酸的定点诱变表明,氧化还原活性对于刺激细胞增殖是必需的。添加的125I标记硫氧还蛋白被培养中的细胞摄取,并可能具有细胞内作用。一系列烷基2-咪唑基二硫化物已被证明是人硫氧还蛋白还原酶的竞争性抑制剂,其抑制常数(Ki)值为3.3至8.6微摩尔。这些化合物以2.0至4.0微摩尔的半数抑制浓度(IC50)抑制瑞士3T3细胞的血清依赖性增殖,并且一种化合物以60 nM的IC50值抑制瑞士3T3细胞的硫氧还蛋白依赖性增殖。