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叶酸缺乏、错配修复依赖性凋亡与人类疾病

Folate deficiency, mismatch repair-dependent apoptosis, and human disease.

作者信息

Li Guo Min, Presnell Steven R, Gu Liya

机构信息

Department of Pathology and Laboratory Medicine, Markey Cancer Center, University of Kentucky Medical Center, Lexington, KY 40536, USA.

出版信息

J Nutr Biochem. 2003 Oct;14(10):568-75. doi: 10.1016/s0955-2863(03)00115-3.

Abstract

The vitamin that is most commonly deficient in the American diet is folate. Severe folate deficiency in humans is known to cause megaloblastic anemia and developmental defects, and is associated with an increased incidence of several forms of human cancer. Although the exact mechanisms by which this vitamin deficiency may cause these diseases are not known at the present time, recent work has shown that folate deficiency also causes genomic instability and programmed cell death (or apoptosis). Additionally, it is known that the DNA mismatch repair pathway mediates folate deficiency-induced apoptosis. This review will first describe work suggesting that folate deficiency causes genomic instability and apoptosis, then discuss possible mechanisms by which the mismatch repair pathway could trigger folate deficiency-induced apoptosis, which has either protective or destructive effects on tissue.

摘要

美国饮食中最常见缺乏的维生素是叶酸。已知人类严重缺乏叶酸会导致巨幼细胞贫血和发育缺陷,并与多种人类癌症的发病率增加有关。尽管目前尚不清楚这种维生素缺乏可能导致这些疾病的确切机制,但最近的研究表明,叶酸缺乏还会导致基因组不稳定和程序性细胞死亡(即凋亡)。此外,已知DNA错配修复途径介导叶酸缺乏诱导的凋亡。本综述首先将描述表明叶酸缺乏会导致基因组不稳定和凋亡的研究工作,然后讨论错配修复途径可能触发叶酸缺乏诱导的凋亡的潜在机制,这种凋亡对组织具有保护或破坏作用。

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