Page 76 - Read Online
P. 76

Lonardo. Metab Target Organ Damage 2024;4:7                           Metabolism and
               DOI: 10.20517/mtod.2023.56
                                                                             Target Organ Damage




               Commentary                                                                    Open Access



               Is liver fibrosis a risk factor for gynecological
               cancers?


               Amedeo Lonardo

               Department of Internal Medicine, Azienda Ospedaliero-Universitaria, Modena 41126, Italy.
               Correspondence to: Prof. Amedeo Lonardo, Department of Internal Medicine, Azienda Ospedaliero-Universitaria(-2023), 1135
               Via Giardini, Modena 41126, Italy. E-mail: a.lonardo@libero.it

               How to cite this article: Lonardo A. Is liver fibrosis a risk factor for gynecological cancers? Metab Target Organ Damage 2024;4:7.
               https://dx.doi.org/10.20517/mtod.2023.56
               Received: 15 Dec 2023  First Decision: 30 Jan 2024  Revised: 31 Jan 2024  Accepted: 18 Feb 2024  Published: 22 Feb 2024

               Academic Editors: Natalia Rosso, Mariana Machado  Copy Editor: Yanbing Bai  Production Editor: Yanbing Bai


               Abstract
               A recent study by Crudele et al. reported on the association between surrogate indices of liver fibrosis and risk of
               gynecological cancers among dysmetabolic women. To put this study in context, notions regarding sex dimorphism
               in nonalcoholic fatty liver disease (NAFLD) are discussed. Additionally, meta-analytic reviews regarding the risk of
               extrahepatic cancers are reviewed. Next, I discuss the relationship of metabolic dysfunction-associated fatty liver
               disease (MAFLD) with extrahepatic cancers, notably including the breast and cancers of the female reproductive
               systems in humans. The pathomechanisms potentially accounting for this association include genetics, deregulated
               sex hormones, chronic subclinical inflammatory state, dysmetabolic milieu, oxidative stress, gut dysbiosis,
               environmental pollution, and altered immune surveillance.

               Keywords: Breast cancer, uterine cancer, NAFLD, MAFLD



               NAFLD AND GYNECOLOGICAL CANCERS
               In the 1980s, when the definitions of nonalcoholic steatohepatitis (NASH) and nonalcoholic fatty liver
               disease (NAFLD) were first coined , the primary concern of hepatologists was that a subset of NAFLD/
                                             [1,2]
               NASH individuals were at risk of progressing to cirrhosis. However, advancement of science has shown that
               the majority of (non-cirrhotic) NAFLD patients die from liver-unrelated causes, i.e., cardiovascular and
               extrahepatic cancers . While the former outcome may be predicted owing to the strong association
                                 [3]





                           © The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing,
                           adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
               long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and
               indicate if changes were made.

                                                                                       www.oaepublish.com/mtod
   71   72   73   74   75   76   77   78   79   80   81