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散发性结直肠癌发生中的代谢途径:一项新提议。

Metabolic pathways in sporadic colorectal carcinogenesis: A new proposal.

作者信息

Caramujo-Balseiro Sandra, Faro Carlos, Carvalho Lina

机构信息

Institute of Anatomical and Molecular Pathology, Faculty of Medicine - University of Coimbra, Coimbra, Portugal; Department of Life Sciences - University of Coimbra, Coimbra, Portugal.

Department of Life Sciences - University of Coimbra, Coimbra, Portugal; UC Biotech, Cantanhede, Portugal.

出版信息

Med Hypotheses. 2021 Mar;148:110512. doi: 10.1016/j.mehy.2021.110512. Epub 2021 Jan 26.

Abstract

Given the reports made about geographical differences in Colorectal Cancer (CRC) occurrence, suggesting a link between dietary habits, genes and cancer risk, we hypothesise that there are four fundamental metabolic pathways involved in diet-genes interactions, directly implicated in colorectal carcinogenesis: folate metabolism; lipid metabolism; oxidative stress response; and inflammatory response. Supporting this hypothesis are the evidence given by the significant associations between several diet-genes polymorphisms and CRC, namely: MTHFR, MTR, MTRR and TS (involved in folate metabolism); NPY, APOA1, APOB, APOC3, APOE, CETP, LPL and PON1 (involved in lipid metabolism); MNSOD, SOD3, CAT, GSTP1, GSTT1 and GSTM1 (involved in oxidative stress response); and IL-1, IL-6, TNF-α, and TGF-β (involved in inflammatory response). We also highlight the association between some foods/nutrients/nutraceuticals that are important in CRC prevention or treatment and the four metabolic pathways proposed, and the recent results of genome-wide association studies, both assisting our hypothesis. Finally, we propose a new line of investigation with larger studies, using accurate dietary biomarkers and investigating the four metabolic pathways genes simultaneously. This line of investigation will be essential to understand the full complexity of the association between nature and nurture in CRC and perhaps in other types of cancers. Only with this in-depth knowledge will it be possible to make personalised nutrition recommendations for disease prevention and management.

摘要

鉴于有关结直肠癌(CRC)发生存在地理差异的报道,提示饮食习惯、基因与癌症风险之间存在联系,我们推测有四条基本代谢途径参与饮食与基因的相互作用,直接与结直肠癌的发生有关:叶酸代谢;脂质代谢;氧化应激反应;以及炎症反应。支持这一假设的是一些饮食基因多态性与CRC之间显著关联所提供的证据,即:MTHFR、MTR、MTRR和TS(参与叶酸代谢);NPY、APOA1、APOB、APOC3、APOE、CETP、LPL和PON1(参与脂质代谢);MNSOD、SOD3、CAT、GSTP1、GSTT1和GSTM1(参与氧化应激反应);以及IL-1、IL-6、TNF-α和TGF-β(参与炎症反应)。我们还强调了一些在CRC预防或治疗中重要的食物/营养素/营养保健品与所提出的四条代谢途径之间的关联,以及全基因组关联研究的最新结果,两者均支持我们的假设。最后,我们提出了一个新的研究方向,即开展更大规模的研究,使用准确的饮食生物标志物并同时研究四条代谢途径的基因。这一研究方向对于理解CRC以及或许其他类型癌症中先天因素与后天因素关联的全部复杂性至关重要。只有具备这种深入的知识,才有可能针对疾病预防和管理提出个性化的营养建议。

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