脱氮酶
泛素
蛋白酶体
生物
计算生物学
细胞生物学
生物化学
基因
作者
Pershang Farshi,Rahul Deshmukh,Joseph O. Nwankwo,Richard T Arkwright,Boris Cvek,Jinbao Liu,Q. Ping Dou
标识
DOI:10.1517/13543776.2015.1056737
摘要
The FDA's approval of the 20S proteasome inhibitors (PIs): bortezomib and carfilzomib for treatment of hematological malignancies established the UPS as an anti-cancer target. Unfortunately, many patients are inherently resistant or develop resistance to PIs. One potential strategy to combat PI resistance is targeting upstream components of the UPS such as DUBs. DUBs represent a promising potential therapeutic target due to their critical roles in various cellular processes including protein turnover, localization and cellular homeostasis. While considerable efforts have been undertaken to develop DUB modulators, significant advancements are necessary to move DUBis into the clinic.
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