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首页> 外文期刊>FEBS letters. >Protein kinase PKC delta and c-Abl are required for mitochondrial apoptosis induction by genotoxic stress in the absence of p53, p73 and Fas receptor
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Protein kinase PKC delta and c-Abl are required for mitochondrial apoptosis induction by genotoxic stress in the absence of p53, p73 and Fas receptor

机译:在缺乏p53,p73和Fas受体的情况下,通过基因毒性应激诱导线粒体凋亡需要蛋白激酶PKCδ和c-Abl

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摘要

Doxorubicin, cis-diamminedichloroplatinum (II) and 5-fluorouracil used in chemotherapy induce apoptosis in Hep3B cells in the absence of p53, p73, and functional Fas. Since mediators remain unknown, the requirement of PKC delta (PKC6) and c-Abl was investigated. Suppression of c-Abl or PKC6 expression using SiRNAs impaired PARP cleavage, Gleevec (R) and/or rottlerin inhibited the induction of the subG1 phase and the increase of reactive oxygen species level. Co-precipitations and phosphorylations to mitochondria of c-Abl, PKC6 and Bcl-X-L/s were induced. A depolarization of the mitochondrial membrane and activations of caspase-2 and -9 were observed. We propose that, in the absence of p53, p73 and Fas, genotoxic drugs could require both PKC6 and c-Abl to induce apoptosis through the mitochondrial pathway. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
机译:在不存在p53,p73和功能性Fas的情况下,用于化学疗法的阿霉素,顺二氨二氯铂(II)和5-氟尿嘧啶诱导Hep3B细胞凋亡。由于介体仍然未知,因此研究了PKCδ(PKC6)和c-Abl的需求。使用SiRNA抑制c-Abl或PKC6表达会损害PARP裂解,Gleevec(R)和/或rottlerin抑制了subG1相的诱导和活性氧水平的提高。诱导共沉淀和磷酸化的线粒体的c-Abl,PKC6和Bcl-X-L / s。观察到线粒体膜的去极化以及caspase-2和-9的激活。我们建议,在没有p53,p73和Fas的情况下,基因毒性药物可能需要PKC6和c-Abl才能通过线粒体途径诱导细胞凋亡。 (c)2006年欧洲生物化学学会联合会。由Elsevier B.V.发布。保留所有权利。

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