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维生素 C - 癌症表观基因组调控的新角色。

Vitamin C - A new player in regulation of the cancer epigenome.

机构信息

Department of Hematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark; Biotech Research and Innovation Centre (BRIC), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.

Van Andel Research Institute, Grand Rapids, MI, USA.

出版信息

Semin Cancer Biol. 2018 Aug;51:59-67. doi: 10.1016/j.semcancer.2017.11.001. Epub 2017 Nov 2.

Abstract

Over the past few years it has become clear that vitamin C, as a provider of reduced iron, is an essential factor for the function of epigenetic regulators that initiate the demethylation of DNA and histones. Vitamin C deficiency is rare in the general population, but is frequently observed in patients with cancer. Genes encoding epigenetic regulators are often mutated in cancer, underscoring their central roles in carcinogenesis. In hematological cancers, such as acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), drugs that reverse epigenetic aberrations are now the standard of care. Recent in vitro studies suggest that vitamin C at physiological concentrations, combined with hypomethylating agents may act synergistically to cause DNA demethylation through active and passive mechanisms, respectively. Additionally, several recent studies have renewed interest in the use of pharmacological doses of vitamin C injected intravenously to selectively kill tumor cells. This review will focus on the potential of vitamin C to optimize the outcome of epigenetic therapy in cancer patients and alternatively to act as a therapeutic at high doses.

摘要

在过去的几年中,人们已经清楚地认识到,维生素 C 作为还原态铁的供体,是启动 DNA 和组蛋白去甲基化的表观遗传调节剂发挥功能所必需的因素。维生素 C 缺乏在普通人群中很少见,但在癌症患者中经常观察到。编码表观遗传调节剂的基因在癌症中经常发生突变,这突出了它们在癌症发生中的核心作用。在血液系统癌症(如急性髓细胞白血病(AML)和骨髓增生异常综合征(MDS))中,逆转表观遗传异常的药物现在是标准的治疗方法。最近的体外研究表明,生理浓度的维生素 C 与低甲基化剂联合使用可能通过主动和被动机制分别协同作用导致 DNA 去甲基化。此外,最近的几项研究重新引起了人们对静脉注射大剂量药理剂量维生素 C 选择性杀伤肿瘤细胞的兴趣。本文综述了维生素 C 优化癌症患者表观遗传治疗效果的潜力,并探讨了大剂量维生素 C 作为治疗药物的作用。

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