Tsai Tsung-Chang, Huang Hui-Pei, Chang Kai-Ting, Wang Chau-Jong, Chang Yun-Ching
Superintendent Office, Antai Medical Care Cooperation, Antai Tian-Sheng Memorial Hospital, Pingtung, Taiwan.
Department of Biochemistry, School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Environ Toxicol. 2017 Apr;32(4):1290-1304. doi: 10.1002/tox.22324. Epub 2016 Jul 22.
Cell cycle regulation is an important issue in cancer therapy. Delphinidin and cyanidin are two major anthocyanins of the roselle plant (Hibiscus sabdariffa). In the present study, we investigated the effect of Hibiscus anthocyanins (HAs) on cell cycle arrest in human leukemia cell line HL-60 and the analyzed the underlying molecular mechanisms. HAs extracted from roselle calyces (purity 90%) markedly induced G2/M arrest evaluated with flow cytometry analysis. Western blot analyses revealed that HAs (0.1-0.7 mg mL ) induced G2/M arrest via increasing Tyr15 phosphorylation of Cdc2, and inducing Cdk inhibitors p27 and p21. HAs also induced phosphorylation of upstream signals related to G2/M arrest such as phosphorylation of Cdc25C tyrosine phosphatase at Ser216, increasing the binding of pCdc25C with 14-3-3 protein. HAs-induced phosphorylation of Cdc25C could be activated by ATM checkpoint kinases, Chk1, and Chk2. We first time confirmed that ATM-Chk1/2-Cdc25C pathway as a critical mechanism for G2/M arrest in HAs-induced leukemia cell cycle arrest, indicating that this compound could be a promising anticancer candidate or chemopreventive agents for further investigation. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 1290-1304, 2017.
细胞周期调控是癌症治疗中的一个重要问题。飞燕草素和矢车菊素是玫瑰茄植物(Hibiscus sabdariffa)中的两种主要花青素。在本研究中,我们研究了玫瑰茄花青素(HAs)对人白血病细胞系HL-60细胞周期阻滞的影响,并分析了其潜在的分子机制。从玫瑰茄花萼中提取的HAs(纯度90%)通过流式细胞术分析显著诱导G2/M期阻滞。蛋白质免疫印迹分析显示,HAs(0.1 - 0.7 mg/mL)通过增加Cdc2的Tyr15磷酸化以及诱导细胞周期蛋白依赖性激酶抑制剂p27和p21来诱导G2/M期阻滞。HAs还诱导了与G2/M期阻滞相关的上游信号的磷酸化,如Cdc25C酪氨酸磷酸酶在Ser216位点的磷酸化,增加了pCdc25C与14-3-3蛋白的结合。HAs诱导的Cdc25C磷酸化可被ATM检查点激酶、Chk1和Chk2激活。我们首次证实ATM-Chk1/2-Cdc25C通路是HAs诱导白血病细胞周期阻滞中G2/M期阻滞的关键机制,表明该化合物可能是一种有前景的抗癌候选物或化学预防剂,有待进一步研究。© 2016威利期刊公司。环境毒理学32: 1290 - 1304, 2017。