AK-1, a SIRT2 inhibitor, destabilizes HIF-1α and diminishes its transcriptional activity during hypoxia

被引:20
|
作者
Lee, So Dam [1 ]
Kim, Wootae [1 ,2 ]
Jeong, Joo-Won [1 ,3 ]
Park, Jong-Wan [4 ]
Kim, Ja-Eun [1 ,2 ]
机构
[1] Kyung Hee Univ, Grad Sch, Dept Biomed Sci, Seoul 02447, South Korea
[2] Kyung Hee Univ, Sch Med, Dept Pharmacol, Seoul 02447, South Korea
[3] Kyung Hee Univ, Sch Med, Dept Anat & Neurobiol, Seoul 02447, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
关键词
SIRT2; AK-1; HIF-1; alpha; Hypoxia; Cancer; TUMOR-SUPPRESSOR PROTEIN; INDUCIBLE FACTORS; CELL-DEATH; BNIP3; HYDROXYLATION; HOMEOSTASIS; METABOLISM; REGULATORS; INDUCTION; RESPONSES;
D O I
10.1016/j.canlet.2016.01.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sirtuin family proteins are involved in the regulation of hypoxic responses which are primarily dependent on a hypoxia-inducible factor (HIF). However, few studies have examined the use of sirtuin inhibitors to regulate HIF. The present study examined the effect of a SIRT2-specific inhibitor, AK-1, on hypoxic responses. Under hypoxic conditions, AK-1 increased the ubiquitination of HIF-1 alpha in a VHL-dependent manner, leading to the degradation of HIF-1a via a proteasomal pathway. Downregulation of HIF-1a expression reduced its transcriptional activity and, eventually, reduced the expression of BNIP3, one of HIF-1 target genes, in AK-1-treated cells. These data demonstrate that SIRT2 inhibition attenuates hypoxic responses, and that SIRT2 inhibitors may have potential as treatments for hypoxia-associated pathological conditions. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
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