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中药单体延胡索甲素(YHL-14)通过非依赖 p53 蛋白的级联反应上调 p21 蛋白表达,诱导人癌细胞 G2/M 期阻滞。

The Chinese herb isolate yuanhuacine (YHL-14) induces G2/M arrest in human cancer cells by up-regulating p21 protein expression through an p53 protein-independent cascade.

机构信息

Nelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, New York 10987; Key Laboratory of Structure-based Drug Design and Discovery, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China.

Nelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, New York 10987.

出版信息

J Biol Chem. 2014 Mar 7;289(10):6394-6403. doi: 10.1074/jbc.M113.513960. Epub 2014 Jan 22.

Abstract

Yuanhuacine (YHL-14), the major component of daphnane diterpene ester isolated from the flower buds of Daphne genkwa, has been reported to have activity against cell proliferation in various cancer cell lines. Nevertheless, the potential mechanism has not been explored yet. Here we demonstrate that YHL-14 inhibits bladder and colon cancer cell growth through up-regulation of p21 expression in an Sp1-dependent manner. We found that YHL-14 treatment resulted in up-regulation of p21 expression and a significant G2/M phase arrest in T24T and HCT116 cells without affecting p53 protein expression and activation. Further studies indicate that p21 induction by YHL-14 occurs at the transcriptional level via up-regulation of Sp1 protein expression. Moreover, our results show that p38 is essential for YHL-14-mediated Sp1 protein stabilization, G2/M growth arrest induction, and anchorage-independent growth inhibition of cancer cells. Taken together, our studies demonstrate a novel mechanism of YHL-14 against cancer cell growth in bladder and colon cancer cell lines, which provides valuable information for the design and synthesis of other new conformation-constrained derivatives on the basis of the structure of YHL-14 for cancer therapy.

摘要

芫花素(YHL-14)是从芫花花蕾中分离得到的达玛烷二萜酯的主要成分,已被报道具有抑制多种癌细胞系增殖的活性。然而,其潜在的机制尚未被探索。在这里,我们证明 YHL-14 通过 Sp1 依赖性方式上调 p21 表达来抑制膀胱和结肠癌细胞生长。我们发现 YHL-14 处理导致 T24T 和 HCT116 细胞中 p21 表达上调,并导致显著的 G2/M 期阻滞,而不影响 p53 蛋白表达和激活。进一步的研究表明,YHL-14 通过上调 Sp1 蛋白表达在转录水平诱导 p21 诱导。此外,我们的结果表明,p38 对于 YHL-14 介导的 Sp1 蛋白稳定、G2/M 生长阻滞诱导和癌细胞锚定独立生长抑制是必不可少的。总之,我们的研究证明了 YHL-14 在膀胱和结肠癌细胞系中抑制癌细胞生长的一种新机制,为基于 YHL-14 结构设计和合成其他新的构象约束衍生物用于癌症治疗提供了有价值的信息。

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本文引用的文献

1
Celastrol decreases specificity proteins (Sp) and fibroblast growth factor receptor-3 (FGFR3) in bladder cancer cells.
Carcinogenesis. 2012 Apr;33(4):886-94. doi: 10.1093/carcin/bgs102. Epub 2012 Feb 14.
3
A cross-talk between NFAT and NF-κB pathways is crucial for nickel-induced COX-2 expression in Beas-2B cells.
Curr Cancer Drug Targets. 2011 Jun;11(5):548-59. doi: 10.2174/156800911795656001.
4
Global cancer statistics.
CA Cancer J Clin. 2011 Mar-Apr;61(2):69-90. doi: 10.3322/caac.20107. Epub 2011 Feb 4.
6
p27 suppresses arsenite-induced Hsp27/Hsp70 expression through inhibiting JNK2/c-Jun- and HSF-1-dependent pathways.
J Biol Chem. 2010 Aug 20;285(34):26058-65. doi: 10.1074/jbc.M110.100271. Epub 2010 Jun 21.
7
Inhibition of NFkappaB and pancreatic cancer cell and tumor growth by curcumin is dependent on specificity protein down-regulation.
J Biol Chem. 2010 Aug 13;285(33):25332-44. doi: 10.1074/jbc.M109.095240. Epub 2010 Jun 9.
8
RhoGDI signaling provides targets for cancer therapy.
Eur J Cancer. 2010 May;46(7):1252-9. doi: 10.1016/j.ejca.2010.02.025. Epub 2010 Mar 27.
10
JNK1 mediates degradation HIF-1alpha by a VHL-independent mechanism that involves the chaperones Hsp90/Hsp70.
Cancer Res. 2010 Jan 15;70(2):813-23. doi: 10.1158/0008-5472.CAN-09-0448. Epub 2010 Jan 12.

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