Competitive inhibition by NAG-1/GDF-15 NLS peptide enhances its anti-cancer activity

被引:15
|
作者
Lee, Jaehak [1 ,2 ]
Kim, Ilju [1 ,2 ]
Yoo, Eunsu [1 ,2 ]
Baek, Seung Joon [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Lab Signal Transduct, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Res Inst Vet Sci, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
GDF15; NAG-1; Nuclear localization signal; Peptide transfection; Mitochondrial membrane potential; High-content screening; ACTIVATED GENE-1; CANCER CELLS; BETA; CYTOKINE-1; APOPTOSIS; MEMBER; RECEPTOR; CLONING; TARGET; GDF15;
D O I
10.1016/j.bbrc.2019.08.090
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
Non-steroidal anti-inflammatory drug activated gene-1 (NAG-1), also known as growth differentiation factor 15 (GDF15), is a TGF-beta (transforming growth factor beta) superfamily protein with a distinctive secretion pathway. NAG-1 is associated with multiple diseases including cancer, wherein it plays a role in both pro- and anti-cancer activities. We previously reported that NAG-1 is translocated to different subcellular compartments and its activity depends on its localization. In this paper, we report that the transfection of a novel peptide corresponding to the nuclear localization signal (NLS) of NAG-1 blocks its translocation to the nucleus. Further, accumulation of NAG-1 in the cytoplasm decreased mitochondrial membrane potential, thus implying apoptosis induction as a consequence. Overall, our results indicate that the novel peptide derived from NAG-1 NLS sequence is a promising tool for enhancing the anti-tumorigenic activity of NAG-1. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:29 / 34
页数:6
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