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Cell Death in Hepatocellular Carcinoma: Pathogenesis and Therapeutic Opportunities.
García-Pras, Ester; Fernández-Iglesias, Anabel; Gracia-Sancho, Jordi; Pérez-Del-Pulgar, Sofía.
Afiliación
  • García-Pras E; Liver Unit, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERHED, 08036 Barcelona, Spain.
  • Fernández-Iglesias A; Liver Vascular Biology Research Group, IDIBAPS, CIBEREHD, 08036 Barcelona, Spain.
  • Gracia-Sancho J; Liver Vascular Biology Research Group, IDIBAPS, CIBEREHD, 08036 Barcelona, Spain.
  • Pérez-Del-Pulgar S; Department for Biomedical Research, Hepatology, Inselspital, University of Bern, 3008 Bern, Switzerland.
Cancers (Basel) ; 14(1)2021 Dec 23.
Article en En | MEDLINE | ID: mdl-35008212
Hepatocellular carcinoma (HCC) is the most prevalent primary liver cancer and the third leading cause of cancer death worldwide. Closely associated with liver inflammation and fibrosis, hepatocyte cell death is a common trigger for acute and chronic liver disease arising from different etiologies, including viral hepatitis, alcohol abuse, and fatty liver. In this review, we discuss the contribution of different types of cell death, including apoptosis, necroptosis, pyroptosis, or autophagy, to the progression of liver disease and the development of HCC. Interestingly, inflammasomes have recently emerged as pivotal innate sensors with a highly pathogenic role in various liver diseases. In this regard, an increased inflammatory response would act as a key element promoting a pro-oncogenic microenvironment that may result not only in tumor growth, but also in the formation of a premetastatic niche. Importantly, nonparenchymal hepatic cells, such as liver sinusoidal endothelial cells, hepatic stellate cells, and hepatic macrophages, play an important role in establishing the tumor microenvironment, stimulating tumorigenesis by paracrine communication through cytokines and/or angiocrine factors. Finally, we update the potential therapeutic options to inhibit tumorigenesis, and we propose different mechanisms to consider in the tumor microenvironment field for HCC resolution.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: Cancers (Basel) Año: 2021 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: Cancers (Basel) Año: 2021 Tipo del documento: Article País de afiliación: España Pais de publicación: Suiza