三氧化二砷
急性早幼粒细胞白血病
癌症研究
癌症
药品
化学
癌症治疗
药理学
医学
生物信息学
生物
砷
内科学
有机化学
基因
维甲酸
生物化学
作者
Md Wahiduzzaman,Akinobu Ota,Yoshitaka Hosokawa
出处
期刊:Current Cancer Drug Targets
[Bentham Science]
日期:2020-02-11
卷期号:20 (2): 115-129
被引量:9
标识
DOI:10.2174/1568009619666191021122006
摘要
Arsenic, a naturally-occurring toxic element, and a traditionally-used drug, has received a great deal of attention worldwide due to its curative anti-cancer properties in patients with acute promyelocytic leukemia. Among the arsenicals, arsenic trioxide has been most widely used as an anti-cancer drug. Recent advances in cancer therapeutics have led to a paradigm shift away from traditional cytotoxic drugs towards the targeting of proteins closely associated with driving the cancer phenotype. Due to the diverse anti-cancer effects of ATO on different types of malignancies, numerous studies have made efforts to uncover the mechanisms of ATO-induced tumor suppression. From in vitro cellular models to studies in clinical settings, ATO has been extensively studied. The outcomes of these studies have opened doors to establishing improved molecular-targeted therapies for cancer treatment. The efficacy of ATO has been augmented by combination with other drugs. In this review, we discuss recent arsenic-based cancer therapies and summarize the novel underlying molecular mechanisms of the anti-cancer effects of ATO.
科研通智能强力驱动
Strongly Powered by AbleSci AI