好斗的
HDAC6型
蛋白酶体
自噬
细胞生物学
伴侣(临床)
组蛋白脱乙酰基酶
细胞内
蛋白质聚集
蛋白质降解
曲古抑菌素A
生物
化学
癌症研究
组蛋白
细胞凋亡
医学
生物化学
病理
基因
作者
Agustı́n Rodrı́guez-González,Tara L. Lin,Alan K. Ikeda,Tiffany Simms-Waldrip,Cecilia Fu,Kathleen M. Sakamoto
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2008-04-15
卷期号:68 (8): 2557-2560
被引量:176
标识
DOI:10.1158/0008-5472.can-07-5989
摘要
Abstract Misfolded or aggregated proteins have two fates: they are either refolded with the help of chaperones or degraded by the proteasome. Cells also have an alternative pathway that involves intracellular “storage bins” for misfolded intracellular proteins known as aggresomes. Aggresomes recruit motor proteins that transport misfolded or aggregated proteins to chaperones and proteasomes for subsequent destruction. There is emerging evidence that inhibiting the aggresome pathway leads to accumulation of misfolded proteins and apoptosis in tumor cells through autophagy. We discuss the role of aggresomes in cancer and the potential to target this pathway for therapy. [Cancer Res 2008;68(8):2557–60]
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