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含死亡结构域的p53诱导蛋白(Pidd)的表达与口腔鳞状细胞癌中的细胞凋亡

The expression of p53-induced protein with death domain (Pidd) and apoptosis in oral squamous cell carcinoma.

作者信息

Bradley G, Tremblay S, Irish J, MacMillan C, Baker G, Gullane P, Benchimol S

机构信息

Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.

出版信息

Br J Cancer. 2007 May 7;96(9):1425-32. doi: 10.1038/sj.bjc.6603745. Epub 2007 Apr 17.

Abstract

The Pidd (p53-induced protein with death domain) gene was shown to be induced by the tumour suppressor p53 and to mediate p53-dependent apoptosis in mouse and human cells, through interactions with components of both the mitochondrial and the death receptor signalling pathways. To study the role of Pidd in clinical tumours, we measured its expression by quantitative reverse transcription-PCR in microdissected oral squamous cell carcinomas (OSCC) with and without p53 mutation. Tumour cell apoptosis was assessed by in situ terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling. Tumour proliferation was assessed by immunohistochemical staining for the Ki-67 antigen. We found a wide range of Pidd expression among OSCC. Statistical analysis revealed an association between Pidd expression and apoptotic index (Mann-Whitney test, P<0.001), consistent with a role of Pidd in apoptosis in this tumour type. Furthermore, we showed a positive correlation between apoptotic index and proliferative index that has not been previously described for OSCC. There was no correlation between Pidd expression and the p53 mutation status of these tumours, suggesting that Pidd expression may be regulated by p53-independent mechanisms. Further characterisation of these molecular defects in the control of proliferation and apoptosis should help in developing treatments that target OSCC according to their biological properties.

摘要

Pidd(含死亡结构域的p53诱导蛋白)基因已被证明可由肿瘤抑制因子p53诱导产生,并通过与线粒体和死亡受体信号通路的成分相互作用,在小鼠和人类细胞中介导p53依赖性凋亡。为了研究Pidd在临床肿瘤中的作用,我们通过定量逆转录PCR检测了有或无p53突变的显微切割口腔鳞状细胞癌(OSCC)中Pidd的表达。通过原位末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法评估肿瘤细胞凋亡。通过Ki-67抗原的免疫组织化学染色评估肿瘤增殖。我们发现OSCC中Pidd的表达范围很广。统计分析显示Pidd表达与凋亡指数之间存在关联(Mann-Whitney检验,P<0.001),这与Pidd在这种肿瘤类型的凋亡中所起的作用一致。此外,我们还发现凋亡指数与增殖指数之间呈正相关,这在OSCC中此前尚未有过描述。Pidd表达与这些肿瘤的p53突变状态之间没有相关性,这表明Pidd的表达可能受p53非依赖性机制调控。进一步表征这些在增殖和凋亡调控中的分子缺陷,应有助于根据OSCC的生物学特性开发靶向治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e9c/2360189/30f7faf3ba7e/6603745f1.jpg

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