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藏红花素通过诱导蛋白酪氨酸磷酸酶SHP-1抑制组成型激活的STAT3。

Crocin Suppresses Constitutively Active STAT3 Through Induction of Protein Tyrosine Phosphatase SHP-1.

作者信息

Kim Buyun, Lee Ki Yong, Park Byoungduck

机构信息

College of Pharmacy, Keimyung University, 1095 Dalgubeoldaero, Dalseo-Gu, Daegu 704-701, Republic of Korea.

College of Pharmacy, Korea University, Sejong Campus 2511 Sejong-ro, Sejong City 339-770, Republic of Korea.

出版信息

J Cell Biochem. 2017 Oct;118(10):3290-3298. doi: 10.1002/jcb.25980. Epub 2017 May 3.

DOI:10.1002/jcb.25980
PMID:28295507
Abstract

The aim of the present study is to investigate the effect of a natural compound crocin, one of the active components of saffron, on human multiple myeloma cells. Crocin effectively suppressed constitutive STAT3 activation, translocation of STAT3 to the nucleus, and its target gene expression. The suppression of STAT3 was mediated through the inhibition of activation of protein tyrosine kinases JAK1, JAK2, and c-Src. We found that crocin induced the expression of SHP-1, a tyrosine protein phosphatase, and pervanadate treatment reversed the crocin-induced downregulation of STAT3, suggesting the involvement of a protein tyrosine phosphatase. Moreover, suppression of SHP-1 by its inhibitor overturned the effect of crocin on induction of SHP-1 and the inhibition of STAT3 activation. Finally, crocin downregulated the expression of STAT3-mediated gene products including anti-apoptotic (Bcl-2), pro-apoptotic (BAX), invasive (CXCR4), angiogenic (VEGF), and cell cycle regulator (cyclin D1), which are correlated with suppression of proliferation, the accumulation of cells in sub-G1 phase of cell cycle, and induction of apoptosis. Overall, our results suggested that crocin is a novel inhibitor of STAT3 activation pathway and thus may have potential in prevention and treatment of human multiple myeloma. J. Cell. Biochem. 118: 3290-3298, 2017. © 2017 Wiley Periodicals, Inc.

摘要

本研究的目的是调查天然化合物藏红花素(番红花的活性成分之一)对人多发性骨髓瘤细胞的影响。藏红花素有效抑制组成型STAT3激活、STAT3向细胞核的转位及其靶基因表达。STAT3的抑制是通过抑制蛋白酪氨酸激酶JAK1、JAK2和c-Src的激活介导的。我们发现藏红花素诱导酪氨酸蛋白磷酸酶SHP-1的表达,过钒酸盐处理逆转了藏红花素诱导的STAT3下调,表明蛋白酪氨酸磷酸酶参与其中。此外,其抑制剂对SHP-1的抑制作用推翻了藏红花素对SHP-1诱导和STAT3激活抑制的作用。最后,藏红花素下调了STAT3介导的基因产物的表达,包括抗凋亡基因(Bcl-2)、促凋亡基因(BAX)、侵袭相关基因(CXCR4)、血管生成相关基因(VEGF)和细胞周期调节因子(细胞周期蛋白D1),这些与增殖抑制、细胞周期亚G1期细胞积累和凋亡诱导相关。总体而言,我们的结果表明藏红花素是一种新型的STAT3激活途径抑制剂,因此可能在人类多发性骨髓瘤的预防和治疗中具有潜力。《细胞生物化学杂志》118: 3290 - 3298, 2017年。© 2017威利期刊公司。

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