Department of Pharmacy, Baotou Medical College, Baotou, Inner Mongolia 014040, China.
The Second Affiliated Hospital of Mudanjiang Medical University, Mudanjiang 157000, China.
Curr Top Med Chem. 2021;21(19):1737-1755. doi: 10.2174/1568026621666210813105240.
Notwithstanding the noteworthy advances in its treatment, cancer remains one of the most serious threatens to humans across the world. Hydroxamic acid derivatives, the potential inhibitors of Histone Deacetylases (HDACs), could inhibit cancer cell proliferation, induce cell differentiation, apoptosis and autophagy, and suppress angiogenesis, invasion as well as metastasis through diverse signaling pathways. Thus, hydroxamic acid derivatives exhibit promising activity against cancers and are useful scaffolds in modern anticancer drug discovery. The purpose of the present review article is to summarize the recent developments (Jan, 2011-Jan, 2021) in hydroxamic acid derivatives with insights into their in vivo anticancer potential and mechanisms of action.
尽管在治疗方面取得了显著进展,但癌症仍然是全世界人类面临的最严重威胁之一。羟肟酸衍生物是组蛋白去乙酰化酶(HDACs)的潜在抑制剂,可通过多种信号通路抑制癌细胞增殖、诱导细胞分化、凋亡和自噬,以及抑制血管生成、侵袭和转移。因此,羟肟酸衍生物对癌症具有良好的活性,是现代抗癌药物发现的有用支架。本文综述了 2011 年 1 月至 2021 年 1 月羟肟酸衍生物的最新研究进展,深入探讨了其体内抗癌潜力和作用机制。