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核因子-κB激活与肺癌细胞对肿瘤坏死因子-α诱导凋亡的抗性相关。

NF-kappaB activation is related to the resistance of lung cancer cells to TNF-alpha-induced apoptosis.

作者信息

Kim J Y, Lee S, Hwangbo B, Lee C T, Kim Y W, Han S K, Shim Y S, Yoo C G

机构信息

Department of Internal Medicine, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul, 110-799, Korea.

出版信息

Biochem Biophys Res Commun. 2000 Jun 24;273(1):140-6. doi: 10.1006/bbrc.2000.2909.

Abstract

In diverse cell types, NF-kappaB transcription factors have been shown to have a role in regulating the apoptotic program, either as essential for the induction of apoptosis or, perhaps more commonly, as blockers of apoptosis. We investigated the role of NF-kappaB activation in the TNF-alpha-mediated apoptosis in lung cancer cells. TNF-alpha-resistant NCI-H157 cells became sensitized to TNF-alpha by prior treatment with cycloheximide, suggesting the presence of newly synthesized antiapoptotic protein(s). We next evaluated whether the transcription of antiapoptotic protein(s) depends on the activation of NF-kappaB. NF-kappaB activation was blocked by either adenovirus-mediated overexpression of IkappaBalpha superrepressor or pretreatment with proteasome inhibitor, MG132. Both methods of blocking NF-kappaB activation enhanced TNF-alpha-induced apoptosis in NCI-H157 cells. These results suggest that NF-kappaB activation confers resistance to TNF-alpha-mediated apoptosis in lung cancer cells.

摘要

在多种细胞类型中,核因子-κB转录因子已被证明在调节凋亡程序中发挥作用,既可以作为诱导凋亡所必需的因子,或者更常见的是,作为凋亡的阻滞剂。我们研究了核因子-κB激活在肺癌细胞中肿瘤坏死因子-α介导的凋亡中的作用。对肿瘤坏死因子-α耐药的NCI-H157细胞通过先用放线菌酮处理而对肿瘤坏死因子-α变得敏感,这表明存在新合成的抗凋亡蛋白。接下来我们评估抗凋亡蛋白的转录是否依赖于核因子-κB的激活。核因子-κB的激活通过腺病毒介导的IκBα超级阻遏物的过表达或用蛋白酶体抑制剂MG132预处理来阻断。这两种阻断核因子-κB激活的方法均增强了肿瘤坏死因子-α诱导的NCI-H157细胞凋亡。这些结果表明,核因子-κB激活赋予肺癌细胞对肿瘤坏死因子-α介导的凋亡的抗性。

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