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首页> 外文期刊>Pancreas >Caspase-3 activation downstream from reactive oxygen species in heat-induced apoptosis of pancreatic carcinoma cells carrying a mutant p53 gene.
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Caspase-3 activation downstream from reactive oxygen species in heat-induced apoptosis of pancreatic carcinoma cells carrying a mutant p53 gene.

机译:Caspase-3在活性氧下游下游,在热诱导的携带突变p53基因的胰腺癌细胞凋亡中起作用。

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摘要

In the present study we investigated the intracellular signaling pathway leading to p53-independent activation of caspase-3 during heat-induced apoptosis of pancreatic carcinoma cells. Induction of mutant p53 protein, but not p21/WAF-1, was observed after heat treatment of both heat-resistant (PANC-1) and heat-sensitive (MIAPaCa-2) cells. A specific inhibitor of caspase-3 (Ac-DMQD-CHO) caused 84% and 92% inhibition of apoptosis in MIAPaCa-2 and PANC-1 cells, respectively. Caspase-3 mRNA expression was increased in both cell lines after heat treatment. Further, heat-induced caspase-3 activity detected by fluorogenic assay in MIAPaCa-2 cells was almost completely inhibited by addition of the antioxidant N-acetyl-L-cysteine. In contrast, Ac-DMQD-CHO had no inhibitory effect on amounts of reactive oxygen species in heat-treated MIAPaCa-2 cells. These results suggest a possible pathway by which reactive oxygen species lead to caspase-3 activation to cause heat-induced death of pancreatic carcinoma cells carrying mutant p53.
机译:在本研究中,我们研究了细胞内信号传导途径,该过程在热诱导胰腺癌细胞凋亡过程中导致caspase-3的p53独立活化。热处理耐热(PANC-1)和热敏感(MIAPaCa-2)细胞后,均观察到突变型p53蛋白的诱导,但未诱导p21 / WAF-1的诱导。 caspase-3的特异性抑制剂(Ac-DMQD-CHO)分别导致MIAPaCa-2和PANC-1细胞凋亡的抑制作用分别为84%和92%。热处理后,两种细胞系中的Caspase-3 mRNA表达均增加。此外,通过荧光检测在MIAPaCa-2细胞中检测到的热诱导的caspase-3活性几乎完全被抗氧化剂N-乙酰基-L-半胱氨酸的添加所抑制。相反,Ac-DMQD-CHO对经热处理的MIAPaCa-2细胞中活性氧的含量没有抑制作用。这些结果表明一种可能的途径,其中活性氧导致caspase-3活化,从而导致热诱导携带突变体p53的胰腺癌细胞死亡。

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