Prenylated Rab acceptor RABAC1 inhibits anti-apoptotic protein BCL2A1 and induces apoptosis

被引:10
作者
Kim, Jong-Tae [1 ]
Cho, Hee Jun [1 ]
Cho, Mi-Young [2 ]
Lim, Jeewon [1 ,3 ]
Park, Eun Sun [1 ,3 ]
Lim, Jong-Seok [4 ,5 ]
Lee, Hee Gu [1 ,3 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Immunotherapy Res Ctr, Daejeon, South Korea
[2] SKKU Adv Inst Nanotechnol, Suwon, South Korea
[3] Univ Sci & Technol, Dept Biomol Sci, Daejeon, South Korea
[4] Sookmyung Womens Univ, Dept Biomol Sci, Seoul, South Korea
[5] Sookmyung Womens Univ, Cellular Heterogene Res Ctr, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
RABAC1; PRA; BCL2A1; BCL2; Apoptosis; UP-REGULATION; POTENTIAL MECHANISM; FAMILY PROTEINS; BCL-2; EXPRESSION; CANCER; BFL-1; CHEMORESISTANCE; GTPASES; DISSOCIATION;
D O I
10.1016/j.bbrc.2019.04.080
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
The B cell lymphoma 2 (BCL2) family of proteins constitutes a critical intracellular checkpoint in the intrinsic apoptosis pathway. Among BCL2 members, the anti-apoptotic protein BCL2A1 mediates the resistance to BCL2 inhibitors and may be considered as a target for anti-cancer therapy. Here, we report that prenylated Rab acceptor 1 (RABAC1 or PRA1) inhibits the anti-apoptotic activity of BCL2A1 and induces apoptosis in AGS gastric cancer cells. Protein interaction of BCL2A1 and RABAC1 was verified by an in-vitro glutathione-S-transferase pull-down assay, immunoprecipitation, and confocal microscopy. When apoptosis was induced by cisplatin, the anti-apoptotic activity of BCL2A1 was blocked by RABAC1 expression. RABAC1 caused caspase-3 activation and decreased cell proliferation, clonogenic cell survival, and cell migration and invasion. We suggest RABAC1 as a potential therapeutic target for BCL2A1-related cancer. (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:940 / 946
页数:7
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