Adiponectin accounts for gender differences in hepatocellular carcinoma incidence

Author:

Manieri Elisa12ORCID,Herrera-Melle Leticia1ORCID,Mora Alfonso1ORCID,Tomás-Loba Antonia1,Leiva-Vega Luis1,Fernández Delia I.1,Rodríguez Elena1,Morán Laura34ORCID,Hernández-Cosido Lourdes5,Torres Jorge L.5,Seoane Luisa M.67,Cubero Francisco Javier34ORCID,Marcos Miguel5ORCID,Sabio Guadalupe1ORCID

Affiliation:

1. Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain

2. Centro Nacional de Biotecnología, Madrid, Spain

3. Department of Immunology, Ophthalmology and Otorhinolaryngology, Complutense University School of Medicine, Madrid, Spain

4. 12 de Octubre Health Research Institute, Madrid, Spain

5. University of Salamanca, University Hospital of Salamanca–Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain

6. Fisiopatología Endocrina, Instituto de Investigación Sanitaria de Santiago, Hospital Clínico Universitario de Santiago de Compostela Servicio Gallego de Salud, Santiago de Compostela, Spain

7. Centro de Investigación Biomédica en Red (CIBER), Fisiopatología Obesidad y Nutrición, Instituto Salud Carlos III, Spain

Abstract

Hepatocellular carcinoma (HCC) is the sixth most common cancer type and the fourth leading cause of cancer-related death. This cancer appears with higher incidence in men and during obesity; however, the specific mechanisms underlying this correlation are unknown. Adipose tissue, a key organ in metabolic syndrome, shows evident gender disparities in the production of adipokines. Levels of the important adipokine adiponectin decrease in men during puberty, as well as in the obese state. Here, we show that this decrease in adiponectin levels is responsible for the increased liver cancer risk in males. We found that testosterone activates the protein JNK in mouse and human adipocytes. JNK-mediated inhibition of adiponectin secretion increases liver cancer cell proliferation, since adiponectin protects against liver cancer development through the activation of AMP-activated protein kinase (AMPK) and p38α. This study provides insight into adipose tissue to liver crosstalk and its gender relation during cancer development, having the potential to guide strategies for new cancer therapeutics.

Funder

Ramón y Cajal Program

La Caixa Foundation

Ministerio de Educación, Cultura y Deporte

European Research Council

European Foundation for the Study of Diabetes

Lilly

Ministerio de Ciencia, Innovación y Universidades

Comunidad de Madrid

BBVA Becas Leonardo a Investigadores y Creadores Culturales

Instituto de Salud Carlos III

Federación Española de Enfermedades Raras

Junta de Castilla y León GRS

Ramón y Cajal

Gilead

Ministerio de Economia y Competitividad Retos

The Alan Morement Memorial Fund Cholangiocarcinoma Charity

European Cooperation in Science and Technology Action

European Foundation for Alcohol Research

Pro CNIC Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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