Withaferin A Analogs That Target the AAA plus Chaperone p97

被引:38
作者
Tao, Shasha [1 ]
Tillotson, Joseph [1 ]
Wijeratne, E. M. Kithsiri [2 ]
Xu, Ya-ming [2 ]
Kang, MinJin [1 ]
Wu, Tongde [1 ]
Lau, Eric C. [1 ]
Mesa, Celestina [1 ]
Mason, Damian J. [1 ]
Brown, Robert V. [1 ]
La Clair, James J. [1 ]
Gunatilaka, A. A. Leslie [2 ]
Zhang, Donna D. [1 ]
Chapman, Eli [1 ]
机构
[1] Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
[2] Univ Arizona, Southwest Ctr Nat Prod Res & Commercializat, Coll Agr & Life Sci, Sch Nat Resources & Environm, Tucson, AZ 85706 USA
关键词
WITHANIA-SOMNIFERA; INHIBITORS; ATPASE; UBIQUITIN; VCP/P97; PROTEOSTASIS; ASHWAGANDHA; DEGRADATION; REGULATOR; P97/VCP;
D O I
10.1021/acschembio.5b00367
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the mode of action (MOA) of many natural products can be puzzling with mechanistic clues that seem to lack a common thread. One such puzzle lies in the evaluation of the antitumor properties of the natural product withaferin A (WFA). A variety of seemingly unrelated pathways have been identified to explain its activity, suggesting a lack of selectivity. We now show that WFA acts as an inhibitor of the chaperone, p97, both in vitro and in cell models in addition to inhibiting the proteasome in vitro. Through medicinal chemistry, we have refined the activity of WFA toward p97 and away from the proteasome. Subsequent studies indicated that these WFA analogs retained p97 activity and cytostatic activity in cell models, suggesting that the modes of action reported for WFA could be connected by proteostasis modulation. Through this endeavor, we highlight how the parallel integration of medicinal chemistry with chemical biology offers a potent solution to one of natures' intriguing molecular puzzles.
引用
收藏
页码:1916 / 1924
页数:9
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