Liu Bin, Liu Lixia, Zang Aimin, Song Zizheng, Yang Hua, Wang Zhiyu, Shang Yanhong, Ma Tao, Zhang Yonggang
Department of Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Department of Functions Branch, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Oncol Lett. 2019 Sep;18(3):3317-3322. doi: 10.3892/ol.2019.10658. Epub 2019 Jul 24.
Tanshinone IIA exhibits natural antioxidative and antineoplastic activity. However, to the best of our knowledge, the effects of tanshinone IIA on human nasopharyngeal carcinoma cells remains unknown. The present study aimed to investigate whether tanshinone IIA inhibits proliferation and induces apoptosis of human nasopharyngeal carcinoma cells via p53-cyclin B1/cell division cycle gene 2 (CDC2). Cell proliferation, cytotoxicity and apoptosis of 13-9B cells were evaluated by an MTT assay, lactate dehydrogenase assay and flow cytometry, respectively. ELISA and western blot analysis were used to analyze caspase-3 activity and poly (ADP-ribose) polymerase (PARP), p53, cyclin B1 and CDC2 protein expression in 13-9B cells. Treatment of 13-9B cells with tanshinone IIA significantly suppressed cell proliferation and significantly induced cytotoxicity and apoptosis of 13-9B cells. Furthermore, tanshinone IIA significantly increased caspase-3 activity, and significantly increased the protein expression levels of PARP, p53, cyclin B1 and CDC2 in 13-9B cells. In summary, the current results indicate that tanshinone IIA inhibits proliferation and induces apoptosis of human nasopharyngeal carcinoma cells via PARP, p53, cyclin B1/CDC2 and caspase-3-mediated signaling.
丹参酮IIA具有天然的抗氧化和抗肿瘤活性。然而,据我们所知,丹参酮IIA对人鼻咽癌细胞的作用仍不清楚。本研究旨在探讨丹参酮IIA是否通过p53-细胞周期蛋白B1/细胞分裂周期基因2(CDC2)抑制人鼻咽癌细胞的增殖并诱导其凋亡。分别采用MTT法、乳酸脱氢酶法和流式细胞术评估13-9B细胞的细胞增殖、细胞毒性和凋亡情况。采用ELISA和蛋白质印迹分析来分析13-9B细胞中半胱天冬酶-3活性以及聚(ADP-核糖)聚合酶(PARP)、p53、细胞周期蛋白B1和CDC2的蛋白表达。用丹参酮IIA处理13-9B细胞可显著抑制细胞增殖,并显著诱导13-9B细胞的细胞毒性和凋亡。此外,丹参酮IIA可显著提高13-9B细胞中半胱天冬酶-3活性,并显著提高PARP、p53、细胞周期蛋白B1和CDC2的蛋白表达水平。总之,目前结果表明丹参酮IIA通过PARP、p53、细胞周期蛋白B1/CDC2和半胱天冬酶-3介导的信号通路抑制人鼻咽癌细胞的增殖并诱导其凋亡。