| Literature DB >> 29459767 |
Colin Hockings1,2,3, Amber E Alsop1,2, Stephanie C Fennell1,2, Erinna F Lee4,5,6, W Douglas Fairlie4,5,6, Grant Dewson1,2, Ruth M Kluck7,8.
Abstract
The prosurvival Bcl-2 family proteins Mcl-1 and Bcl-xL inhibit apoptosis by sequestering BH3-only proteins such as Bid and Bim (MODE 1) or the effector proteins Bak and Bax (MODE 2). To better understand the contributions of MODE 1 and MODE 2 in blocking cell death, and thus how to bypass resistance to cell death, we examined prescribed mixtures of Bcl-2 family proteins. In a Bim and Bak mixture, Bcl-xL and Mcl-1 each sequestered not only Bim but also Bak as it became activated by Bim. In contrast, in a Bid and Bak mixture, Bcl-xL preferentially sequestered Bid while Mcl-1 preferentially sequestered Bak. Notably, Bcl-xL could sequester Bak in response to the BH3 mimetic ABT-737, despite this molecule targeting Bcl-xL. These findings highlight the importance of Bak sequestration in resistance to anti-cancer treatments, including BH3 mimetics.Entities:
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Year: 2018 PMID: 29459767 PMCID: PMC5864222 DOI: 10.1038/s41418-017-0010-6
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828