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萝卜硫素诱导的G2/M期细胞周期阻滞涉及关卡激酶2介导的细胞分裂周期蛋白25C磷酸化。

Sulforaphane-induced G2/M phase cell cycle arrest involves checkpoint kinase 2-mediated phosphorylation of cell division cycle 25C.

作者信息

Singh Shivendra V, Herman-Antosiewicz Anna, Singh Ajita V, Lew Karen L, Srivastava Sanjay K, Kamath Ravindra, Brown Kevin D, Zhang Lin, Baskaran Rajasekaran

机构信息

Department of Pharmacology and University of Pittsburgh Cancer Institute, Pittsburgh, PA 15213, USA.

出版信息

J Biol Chem. 2004 Jun 11;279(24):25813-22. doi: 10.1074/jbc.M313538200. Epub 2004 Apr 8.

Abstract

Previously, we showed that sulforaphane (SFN), a naturally occurring cancer chemopreventive agent, effectively inhibits proliferation of PC-3 human prostate cancer cells by causing caspase-9- and caspase-8-mediated apoptosis. Here, we demonstrate that SFN treatment causes an irreversible arrest in the G(2)/M phase of the cell cycle. Cell cycle arrest induced by SFN was associated with a significant decrease in protein levels of cyclin B1, cell division cycle (Cdc) 25B, and Cdc25C, leading to accumulation of Tyr-15-phosphorylated (inactive) cyclin-dependent kinase 1. The SFN-induced decline in Cdc25C protein level was blocked in the presence of proteasome inhibitor lactacystin, but lactacystin did not confer protection against cell cycle arrest. Interestingly, SFN treatment also resulted in a rapid and sustained phosphorylation of Cdc25C at Ser-216, leading to its translocation from the nucleus to the cytoplasm because of increased binding with 14-3-3beta. Increased Ser-216 phosphorylation of Cdc25C upon treatment with SFN was the result of activation of checkpoint kinase 2 (Chk2), which was associated with Ser-1981 phosphorylation of ataxia telangiectasia-mutated, generation of reactive oxygen species, and Ser-139 phosphorylation of histone H2A.X, a sensitive marker for the presence of DNA double-strand breaks. Transient transfection of PC-3 cells with Chk2-specific small interfering RNA duplexes significantly attenuated SFN-induced G(2)/M arrest. HCT116 human colon cancer-derived Chk2(-/-) cells were significantly more resistant to G(2)/M arrest by SFN compared with the wild type HCT116 cells. These findings indicate that Chk2-mediated phosphorylation of Cdc25C plays a major role in irreversible G(2)/M arrest by SFN. Activation of Chk2 in response to DNA damage is well documented, but the present study is the first published report to link Chk2 activation to cell cycle arrest by an isothiocyanate.

摘要

此前,我们发现萝卜硫素(SFN)这种天然存在的癌症化学预防剂可通过引发半胱天冬酶-9和半胱天冬酶-8介导的凋亡,有效抑制PC-3人前列腺癌细胞的增殖。在此,我们证明SFN处理会导致细胞周期在G(2)/M期发生不可逆阻滞。SFN诱导的细胞周期阻滞与细胞周期蛋白B1、细胞分裂周期(Cdc)25B和Cdc25C的蛋白水平显著降低相关,导致酪氨酸-15磷酸化(无活性)的细胞周期蛋白依赖性激酶1积累。在蛋白酶体抑制剂乳胞素存在的情况下,SFN诱导的Cdc25C蛋白水平下降受到阻滞,但乳胞素并未赋予细胞周期阻滞保护作用。有趣的是,SFN处理还导致Cdc25C在丝氨酸-216处迅速且持续磷酸化,由于与14-3-3β的结合增加,导致其从细胞核转运至细胞质。用SFN处理后Cdc25C丝氨酸-216磷酸化增加是检查点激酶2(Chk2)激活的结果,这与共济失调毛细血管扩张症突变体的丝氨酸-1981磷酸化、活性氧的产生以及组蛋白H2A.X的丝氨酸-139磷酸化有关,组蛋白H2A.X是DNA双链断裂存在的敏感标志物。用Chk2特异性小干扰RNA双链体瞬时转染PC-3细胞可显著减弱SFN诱导的G(2)/M阻滞。与野生型HCT116细胞相比,源自人结肠癌的HCT116 Chk2(-/-)细胞对SFN诱导的G(2)/M阻滞具有显著更高的抗性。这些发现表明Chk2介导的Cdc25C磷酸化在SFN诱导的不可逆G(2)/M阻滞中起主要作用。响应DNA损伤时Chk2的激活已有充分记载,但本研究是首次发表的将Chk2激活与异硫氰酸酯诱导的细胞周期阻滞联系起来的报告。

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