Lin Jihong, Zhang Lei, Wang Zhiwei, Guan Qi, Bao Kai, Wu Lan
Department of Geratology, The First Affiliated Hospital, China Medical University, Shenyang, Liaoning 110001, P.R. China.
Department of Circulatory, General Hospital of Fushun Mining Bureau, Fushun, Liaoning 113008, P.R. China.
Oncol Lett. 2021 Dec;22(6):815. doi: 10.3892/ol.2021.13076. Epub 2021 Sep 28.
The combretastatin A-4/oltipraz hybrid (COH), 5-(3-amino-4-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl)-3-1,2-dithiole-3-one (COH-203) is one of the COH compounds synthesized by our previous study, which has been reported to affect a number of cancer cell lines, such as SGC-7901, KB, HT-1080, HepG2, SMMC-7721 and BEL-7402. The sensitivity of human acute leukemia cell lines to COH-203, and the mechanism underlying its anti-proliferative effects remain unknown, which was investigated in the present study. In the present study, it was demonstrated that COH-203 had notable time- and dose-dependent antiproliferative effects on the human acute promyelocytic leukemia HL-60 cell line. Furthermore, COH-203 treatment resulted in cell cycle arrest at G/M phase in a dose-dependent manner, and subsequently induced apoptosis. Western blot analysis revealed that upregulation of cyclin B was associated with G/M arrest. In addition, treatment with COH-203 resulted in downregulated expression of Bcl-2. This result revealed that COH-203-induced apoptosis in HL-60 cells may occur via the mitochondrial pathway in a caspase-dependent manner.
康普瑞他汀A-4/奥替普拉杂合物(COH),即5-(3-氨基-4-甲氧基苯基)-4-(3,4,5-三甲氧基苯基)-3-1,2-二硫杂环戊烯-3-酮(COH-203)是我们前期研究合成的COH类化合物之一,据报道其对多种癌细胞系有影响,如SGC-7901、KB、HT-1080、HepG2、SMMC-7721和BEL-7402。人类急性白血病细胞系对COH-203的敏感性及其抗增殖作用的潜在机制尚不清楚,本研究对此进行了探讨。在本研究中,结果表明COH-203对人急性早幼粒细胞白血病HL-60细胞系具有显著的时间和剂量依赖性抗增殖作用。此外,COH-203处理以剂量依赖性方式导致细胞周期阻滞于G/M期,随后诱导细胞凋亡。蛋白质免疫印迹分析显示,细胞周期蛋白B的上调与G/M期阻滞有关。此外,COH-203处理导致Bcl-2表达下调。该结果表明,COH-203诱导HL-60细胞凋亡可能通过线粒体途径以半胱天冬酶依赖性方式发生。