细胞凋亡
肿瘤坏死因子α
程序性细胞死亡
癌症研究
细胞
坏死
生物
诱导剂
内源性凋亡
免疫学
细胞生物学
半胱氨酸蛋白酶
生物化学
遗传学
基因
作者
Nadia Corazza,Daniela Kassahn,Sabine Jakob,A Badmann,Thomas Brunner
标识
DOI:10.1111/j.1749-6632.2009.04905.x
摘要
The death ligand members of the tumor necrosis factor (TNF) family are potent inducers of apoptosis in a variety of cell types. In particular, TNF‐related apoptosis‐inducing ligand (TRAIL) has recently received much scientific and commercial attention because of its potent tumor cell‐killing activity while leaving normal untransformed cells mostly unaffected. Furthermore, TRAIL strongly synergizes with conventional chemotherapeutic drugs in inducing tumor cell apoptosis, making it a most promising candidate for future cancer therapy. Increasing evidence indicates, however, that TRAIL may also induce or modulate apoptosis in primary cells. A particular concern is the potential side effect of TRAIL‐based tumor therapies in the liver. In this review we summarize some of the recent findings on the role of TRAIL in tumor cell and hepatocyte apoptosis.
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