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Mer Tyrosine Kinase (MERTK) modulates liver fibrosis progression and hepatocellular carcinoma development.
Pipitone, Rosaria Maria; Calvaruso, Vincenza; Di Marco, Lorenza; Di Salvo, Francesca; Gaggianesi, Miriam; Lupo, Giulia; Zito, Rossella; La Mantia, Claudia; Ramazzotti, Matteo; Petta, Salvatore; Di Marco, Vito; Craxì, Antonio; Grimaudo, Stefania.
Afiliação
  • Pipitone RM; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Calvaruso V; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Di Marco L; Gastroenterology Unit, Department of Medical Specialties, University of Modena e Reggio Emilia, Modena, Italy.
  • Di Salvo F; Department of Agricultural, Food and Forest Sciences, University of Palermo, Palermo, Italy.
  • Gaggianesi M; Department of Surgical Oncological and Stomatological Sciences, University of Palermo, Palermo, Italy.
  • Lupo G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Zito R; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • La Mantia C; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Ramazzotti M; Department of Biochemical, Experimental and Clinical Sciences, University of Florence, Florence, Italy.
  • Petta S; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Di Marco V; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Craxì A; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
  • Grimaudo S; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.
Front Immunol ; 13: 926236, 2022.
Article em En | MEDLINE | ID: mdl-36003399
ABSTRACT
MerTK is a tyrosine kinase receptor that belongs to the TAM (Tyro3/Axl/Mer) receptor family. It is involved in different processes including cellular proliferation/survival, cellular adhesion/migration, and release of the inflammatory/anti-inflammatory cytokines. Although it is reported that MERTK polymorphisms affect the severity of viral and metabolic liver diseases, being able to influence fibrosis progression and hepatocellular carcinoma development, the mechanisms remain unknown.

METHODS:

using a microarray approach, we evaluated the liver expression of genes involved in fibrogenesis and hepatocarcinogenesis in patient with chronic hepatitis C (CHC), stratified for MERTK genotype and MERTK expression.

RESULTS:

we found that the rs 4374383 AA homozygosity is associated with lower MERTK expression in CHC patients and that, depending on MERTK genotype, Matrix Metallopeptidase 9 (MMP9), Matrix Metallopeptidase 7 (MMP7), Secreted Frizzled Related Protein 1 (SFRP1) and WNT gene family 11(WNT11) show differential expression in patients with CHC with or without neoplastic progression.

CONCLUSIONS:

our results confirm that MERTK represents a genetic biomarker for progression of liver disease and are suggestive of translational relevance for the study of downstream pathways involved in fibrogenesis and hepatocarcinogenesis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / C-Mer Tirosina Quinase / Cirrose Hepática / Neoplasias Hepáticas Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / C-Mer Tirosina Quinase / Cirrose Hepática / Neoplasias Hepáticas Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article