Cargando…

Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease

Non-alcoholic fatty liver disease (NAFLD) and hepatocellular carcinoma (HCC) show clear evidence of sexual dimorphism, with a significantly higher incidence in males. Among the determining factors that could explain this sex-based difference, the specific distribution of fat by sex has been suggeste...

Descripción completa

Detalles Bibliográficos
Autores principales: Izquierdo, Andrea G., Carreira, Marcos C., Rodriguez-Carnero, Gemma, Perez-Lois, Raquel, Seoane, Luisa M., Casanueva, Felipe F., Crujeiras, Ana B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739425/
https://www.ncbi.nlm.nih.gov/pubmed/36499327
http://dx.doi.org/10.3390/ijms232315002
_version_ 1784847802393690112
author Izquierdo, Andrea G.
Carreira, Marcos C.
Rodriguez-Carnero, Gemma
Perez-Lois, Raquel
Seoane, Luisa M.
Casanueva, Felipe F.
Crujeiras, Ana B.
author_facet Izquierdo, Andrea G.
Carreira, Marcos C.
Rodriguez-Carnero, Gemma
Perez-Lois, Raquel
Seoane, Luisa M.
Casanueva, Felipe F.
Crujeiras, Ana B.
author_sort Izquierdo, Andrea G.
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) and hepatocellular carcinoma (HCC) show clear evidence of sexual dimorphism, with a significantly higher incidence in males. Among the determining factors that could explain this sex-based difference, the specific distribution of fat by sex has been suggested as a primary candidate, since obesity is a relevant risk factor. In this context, obesity, considered a low-grade chronic inflammatory pathology and responsible for the promotion of liver disease, could lead to sexual dimorphism in the expression profile of genes related to tumor development. When we compared the expression levels of genes associated with the early stages of carcinogenesis in the liver between male and female diet-induced obesity (DIO) rats, we observed that the expression pattern was similar in obese male and female animals. Interestingly, the SURVIVIN/BIRC5 oncogene showed a higher expression in male DIO rats than in female DIO and lean rats. This trend related to sexual dimorphism was observed in leukocytes from patients with obesity, although the difference was not statistically significant. In conclusion, this study evidenced a similar pattern in the expression of most carcinogenesis-related genes in the liver, except SUVIVIN/BIRC5, which could be a predictive biomarker of liver carcinogenesis predisposition in male patients with obesity.
format Online
Article
Text
id pubmed-9739425
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97394252022-12-11 Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease Izquierdo, Andrea G. Carreira, Marcos C. Rodriguez-Carnero, Gemma Perez-Lois, Raquel Seoane, Luisa M. Casanueva, Felipe F. Crujeiras, Ana B. Int J Mol Sci Article Non-alcoholic fatty liver disease (NAFLD) and hepatocellular carcinoma (HCC) show clear evidence of sexual dimorphism, with a significantly higher incidence in males. Among the determining factors that could explain this sex-based difference, the specific distribution of fat by sex has been suggested as a primary candidate, since obesity is a relevant risk factor. In this context, obesity, considered a low-grade chronic inflammatory pathology and responsible for the promotion of liver disease, could lead to sexual dimorphism in the expression profile of genes related to tumor development. When we compared the expression levels of genes associated with the early stages of carcinogenesis in the liver between male and female diet-induced obesity (DIO) rats, we observed that the expression pattern was similar in obese male and female animals. Interestingly, the SURVIVIN/BIRC5 oncogene showed a higher expression in male DIO rats than in female DIO and lean rats. This trend related to sexual dimorphism was observed in leukocytes from patients with obesity, although the difference was not statistically significant. In conclusion, this study evidenced a similar pattern in the expression of most carcinogenesis-related genes in the liver, except SUVIVIN/BIRC5, which could be a predictive biomarker of liver carcinogenesis predisposition in male patients with obesity. MDPI 2022-11-30 /pmc/articles/PMC9739425/ /pubmed/36499327 http://dx.doi.org/10.3390/ijms232315002 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Izquierdo, Andrea G.
Carreira, Marcos C.
Rodriguez-Carnero, Gemma
Perez-Lois, Raquel
Seoane, Luisa M.
Casanueva, Felipe F.
Crujeiras, Ana B.
Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title_full Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title_fullStr Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title_full_unstemmed Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title_short Gender Dimorphism in Hepatic Carcinogenesis-Related Gene Expression Associated with Obesity as a Low-Grade Chronic Inflammatory Disease
title_sort gender dimorphism in hepatic carcinogenesis-related gene expression associated with obesity as a low-grade chronic inflammatory disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739425/
https://www.ncbi.nlm.nih.gov/pubmed/36499327
http://dx.doi.org/10.3390/ijms232315002
work_keys_str_mv AT izquierdoandreag genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT carreiramarcosc genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT rodriguezcarnerogemma genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT perezloisraquel genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT seoaneluisam genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT casanuevafelipef genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease
AT crujeirasanab genderdimorphisminhepaticcarcinogenesisrelatedgeneexpressionassociatedwithobesityasalowgradechronicinflammatorydisease