Zhang Liping, Zhou Yanan, Kong Jing, Zhang Li, Yuan Mengqin, Xian Shu, Wang Yanqing, Cheng Yanxiang, Yang Xiaofeng
Department of Obstetrics and Gynecology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shanxi 710061, P.R. China.
Department of Obstetrics and Gynecology, Wuhan Children's Hospital and Wuhan Maternal and Child Healthcare Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430060, P.R. China.
Exp Ther Med. 2020 Dec;20(6):169. doi: 10.3892/etm.2020.9299. Epub 2020 Oct 9.
Cervical cancer is one of the most common types of gynecological tumor, and thus identifying complementary or substitute treatment methods to treat cervical cancer is important. The present study aimed to evaluate the effect of arsenic trioxide (ATO), a traditional Chinese medicine, on cervical cancer cells and its underlying mechanism. MTT, colony formation and Transwell assays were performed to investigate the effects of different concentrations of ATO on cell proliferation and invasion, respectively. Western blotting and reverse transcription-quantitative PCR were applied to measure hypoxia-inducible factor-1α expression (HIF-1α) expression following ATO treatment. Finally, the effects of HIF-1α knockdown on cervical cancer cell proliferation, apoptosis and invasion were evaluated. The results demonstrated that ATO could inhibit cell proliferation and invasion. Moreover, ATO could induce reactive oxygen species production in a time- and dose-dependent manner. ATO could also promote the apoptosis of cervical cancer cells via HIF-1α. Therefore, the present study may provide a theoretical basis for identifying effective molecular targets for the prevention and treatment of cervical cancer.
宫颈癌是最常见的妇科肿瘤类型之一,因此确定治疗宫颈癌的补充或替代治疗方法很重要。本研究旨在评估中药三氧化二砷(ATO)对宫颈癌细胞的作用及其潜在机制。分别进行MTT、集落形成和Transwell实验,以研究不同浓度ATO对细胞增殖和侵袭的影响。采用蛋白质免疫印迹法和逆转录-定量PCR检测ATO处理后缺氧诱导因子-1α(HIF-1α)的表达。最后,评估敲低HIF-1α对宫颈癌细胞增殖、凋亡和侵袭的影响。结果表明,ATO可抑制细胞增殖和侵袭。此外,ATO能以时间和剂量依赖性方式诱导活性氧生成。ATO还可通过HIF-1α促进宫颈癌细胞凋亡。因此,本研究可能为确定宫颈癌预防和治疗的有效分子靶点提供理论依据。