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瘦素信号在肥胖和结直肠癌中的作用。

Leptin Signaling in Obesity and Colorectal Cancer.

机构信息

Department of Genetics, University of Oradea, 410048 Oradea, Romania.

2nd Medical Clinic, Department of Internal Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.

出版信息

Int J Mol Sci. 2022 Apr 24;23(9):4713. doi: 10.3390/ijms23094713.

DOI:10.3390/ijms23094713
PMID:35563103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9102849/
Abstract

Obesity and colorectal cancer (CRC) are among the leading diseases causing deaths in the world, showing a complex multifactorial pathology. Obesity is considered a risk factor in CRC development through inflammation, metabolic, and signaling processes. Leptin is one of the most important adipokines related to obesity and an important proinflammatory marker, mainly expressed in adipose tissue, with many genetic variation profiles, many related influencing factors, and various functions that have been ascribed but not yet fully understood and elucidated, the most important ones being related to energy metabolism, as well as endocrine and immune systems. Aberrant signaling and genetic variations of leptin are correlated with obesity and CRC, with the genetic causality showing both inherited and acquired events, in addition to lifestyle and environmental risk factors; these might also be related to specific pathogenic pathways at different time points. Moreover, mutation gain is a crucial factor enabling the genetic process of CRC. Currently, the inconsistent and insufficient data related to leptin's relationship with obesity and CRC indicate the necessity of further related studies. This review summarizes the current knowledge on leptin genetics and its potential relationship with the main pathogenic pathways of obesity and CRC, in an attempt to understand the molecular mechanisms of these associations, in the context of inconsistent and contradictory data. The understanding of these mechanisms linking obesity and CRC could help to develop novel therapeutic targets and prevention strategies, resulting in a better prognosis and management of these diseases.

摘要

肥胖症和结直肠癌 (CRC) 是全球主要致死疾病之一,表现出复杂的多因素病理。肥胖被认为是 CRC 发展的一个风险因素,通过炎症、代谢和信号转导过程起作用。瘦素是与肥胖相关的最重要的脂肪因子之一,也是一种重要的促炎标志物,主要在脂肪组织中表达,具有许多遗传变异谱、许多相关影响因素和各种功能,但尚未完全理解和阐明,最重要的功能与能量代谢以及内分泌和免疫系统有关。瘦素的信号转导异常和遗传变异与肥胖症和 CRC 相关,遗传因果关系既有遗传性也有获得性事件,除了生活方式和环境风险因素外,还可能与不同时间点的特定发病途径有关。此外,基因突变是 CRC 遗传过程的关键因素。目前,与瘦素与肥胖症和 CRC 的关系相关的不一致和不充分的数据表明需要进一步进行相关研究。本综述总结了目前关于瘦素遗传学及其与肥胖症和 CRC 主要发病途径的潜在关系的知识,试图了解这些关联的分子机制,这些机制在不一致和矛盾的数据背景下进行。了解这些将肥胖症和 CRC 联系起来的机制有助于开发新的治疗靶点和预防策略,从而改善这些疾病的预后和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db4/9102849/2e35d5c8029d/ijms-23-04713-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db4/9102849/938d9042cf59/ijms-23-04713-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db4/9102849/938d9042cf59/ijms-23-04713-g001.jpg
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