死亡受体5/FADD/caspase-8死亡信号在肿瘤转移中的作用

Molecular and cellular pharmacology Pub Date : 2011-01-01
Shi-Yong Sun
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引用次数: 0

摘要

外源性凋亡通路的正常功能是介导细胞凋亡。因此,这一途径通常被认为是宿主免疫监视癌症的关键。然而,许多研究表明,这一途径中的一些关键成分,包括Fas、死亡受体5 (DR5)、Fas相关死亡结构域(FADD)和caspase-8,可能有助于癌症的生长或转移。我们最近对人头颈部肿瘤组织中DR5和caspase-8表达的研究表明,在淋巴结转移患者的肿瘤组织中,高caspase-8单独或与高DR5一起与较差的无病生存和总生存显著相关,提示这些蛋白可能参与了肿瘤转移的正向调节。因此,我们需要进一步了解死亡受体5/FADD/caspase-8死亡信号在肿瘤转移调控中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding the Role of the Death Receptor 5/FADD/caspase-8 Death Signaling in Cancer Metastasis.

The normal function of the extrinsic apoptotic pathway is to mediate apoptosis. Thus, this pathway is generally recognized to be critical in host immune surveillance against cancer. However, many studies have suggested that some key components in this pathway including Fas, death receptor 5 (DR5), Fas-associated death domain (FADD) and caspase-8 may contribute to cancer growth or metastasis. Our recent study on DR5 and caspase-8 expression in human head and neck cancer tissues indicate that high caspase-8 either alone or along with high DR5 in tumor tissue from patients with lymph node metastasis is significantly associated with poor disease-free survival and overall survival, suggesting that these proteins may be involved in positive regulation of cancer metastasis. Thus, efforts should be made to better understand the role of the death receptor 5/FADD/caspase-8 death signaling in regulation of cancer metastasis.

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