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叶酸状况与结直肠癌风险:2016 年更新。

Folate status and colorectal cancer risk: A 2016 update.

机构信息

Schools of Medicine and Nutritional Science & Policy, Tufts University, U.S.D.A. Human Nutrition Research Center at Tufts University, 711 Washington St, Boston, MA 02111, USA; U.S.D.A. Human Nutrition Research Center at Tufts University, USA.

Chief Physician, Internal Medicine-Oncology, The First Affiliated Hospital, University of South China, Henyang, People's Republic of China; U.S.D.A. Human Nutrition Research Center at Tufts University, USA.

出版信息

Mol Aspects Med. 2017 Feb;53:73-79. doi: 10.1016/j.mam.2016.11.010. Epub 2016 Nov 24.

Abstract

The consensus of epidemiologic evidence indicates that an abundant intake of foodstuffs rich in folate conveys protection against the development of colorectal cancer, and perhaps some other common cancers as well. Pre-clinical models substantiate that the relationship is a genuinely causal one. Pre-clinical models have also lent mechanistic insights into the biochemical and molecular pathways by which adequate folate exposure conveys these protective effects, and human studies are beginning to confirm the relevance of this mechanistic understanding to human cancer biology. Enhancement of genetic stability appears to be a major mechanism by which folate sufficiency protects against carcinogenesis. To date, the Wnt signaling cascade has been the pathway most examined in this regard. The relationship between folate exposure and colorectal cancer risk is a complex one, in part because a number of extrinsic and intrinsic factors act as effect modifiers. This review discusses how the intake of the other three B-vitamins integral to the 1-carbon pathway acts as one such effect modifier. In addition, two concepts that remain matters of considerable debate are whether parental intake of folate impacts on subsequent cancer risk in the offspring, and whether excessive intakes of folate may have a paradoxical cancer-promoting effect: observations underlying these two concepts are presented as well.

摘要

流行病学证据的共识表明,大量摄入富含叶酸的食物可以预防结直肠癌的发生,也许还可以预防其他一些常见癌症。临床前模型证实这种关系是真正的因果关系。临床前模型还为充分暴露于叶酸所带来的这些保护作用的生化和分子途径提供了机制上的见解,而人类研究也开始证实这种机制理解与人类癌症生物学的相关性。增强遗传稳定性似乎是叶酸充足防止致癌作用的主要机制。迄今为止,Wnt 信号级联已成为这方面研究最多的途径。叶酸暴露与结直肠癌风险之间的关系很复杂,部分原因是许多外在和内在因素作为效应修饰剂发挥作用。这篇综述讨论了其他三种与 1 碳途径密切相关的 B 族维生素的摄入如何作为这样的效应修饰剂之一。此外,两个仍然存在很大争议的概念是,父母叶酸的摄入是否会影响后代随后的癌症风险,以及叶酸的过量摄入是否会产生矛盾的促癌作用:提出了这两个概念的基础观察结果。

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