Hepatic IR and IGF1R signaling govern distinct metabolic and carcinogenic processes upon PTEN deficiency in the liver

This study underscores the pivotal roles of phosphatase and tensin homolog (PTEN), insulin receptor (IR), and IGF-1 receptor (IGF1R) in controlling liver metabolism, systemic adiposity, and liver cancer progression. Our findings on the distinct and combined effects of these receptors in PTEN-deficient mice offer key insights into the mechanisms driving metabolic dysfunction-associated steatotic liver disease and related hepatocarcinogenesis. In addition, this research reveals the potential of IR and IGF1R as biomarkers in liver cancer development, presenting new opportunities for therapeutic targeting and disease monitoring.

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Publication Details

Journal
JHEP Reports
Published
2024-12-19
DOI
https://doi.org/10.1016/j.jhepr.2024.101305
Citations
6
Primary Topic
PI3K/AKT/mTOR signaling in cancer
Type
article
Field-Weighted Citation Impact
1.40

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article

Hepatic IR and IGF1R signaling govern distinct metabolic and carcinogenic processes upon PTEN deficiency in the liver

Monika Gjorgjieva, Etienne Delangre, Nicolas Calo, Michelangelo Foti et al.
6 citations
JHEP Reports
PI3K/AKT/mTOR signaling in cancer
1.40
article

Hepatic IR and IGF1R signaling govern distinct metabolic and carcinogenic processes upon PTEN deficiency in the liver

Monika Gjorgjieva, Etienne Delangre, Nicolas Calo, Michelangelo Foti, Christine Maeder, Margot Fournier, Flavien Berthou, Cyril Sobolewski, Christine Sempoux, Serge Nef, Dorothea Portius, Marion Peyrou, Jean-Luc Pitetti, Marta Correia de Sousa, Xavier Montet, Lucie Bourgoin, Laurent Vinet, Anne‐Sophie Ay
article en
6 citations

Abstract

This study underscores the pivotal roles of phosphatase and tensin homolog (PTEN), insulin receptor (IR), and IGF-1 receptor (IGF1R) in controlling liver metabolism, systemic adiposity, and liver cancer progression. Our findings on the distinct and combined effects of these receptors in PTEN-deficient mice offer key insights into the mechanisms driving metabolic dysfunction-associated steatotic liver disease and related hepatocarcinogenesis. In addition, this research reveals the potential of IR and IGF1R as biomarkers in liver cancer development, presenting new opportunities for therapeutic targeting and disease monitoring.

JHEP ReportsVol. 7(4)
University of Geneva (CH), University of Lausanne (CH)
National Science Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Good health and well-being
Openalex Percentile: Top 18%
PI3K/AKT/mTOR signaling in cancer
1.40
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