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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by lklinares
Group name EquipeLL
Item Type Journal Article
Title GCN2 inhibition sensitizes arginine-deprived hepatocellular carcinoma cells to senolytic treatment
Creator Missiaen et al.
Author Rindert Missiaen
Author Nicole M. Anderson
Author Laura C. Kim
Author Bailey Nance
Author Michelle Burrows
Author Nicolas Skuli
Author Madeleine Carens
Author Romain Riscal
Author An Steensels
Author Fuming Li
Author M. Celeste Simon
Abstract Hepatocellular carcinoma (HCC) is a typically fatal malignancy exhibiting genetic heterogeneity and limited therapy responses. We demonstrate here that HCCs consistently repress urea cycle gene expression and thereby become auxotrophic for exogenous arginine. Surprisingly, arginine import is uniquely dependent on the cationic amino acid transporter SLC7A1, whose inhibition slows HCC cell growth in vitro and in vivo. Moreover, arginine deprivation engages an integrated stress response that promotes HCC cell-cycle arrest and quiescence, dependent on the general control nonderepressible 2 (GCN2) kinase. Inhibiting GCN2 in arginine-deprived HCC cells promotes a senescent phenotype instead, rendering these cells vulnerable to senolytic compounds. Preclinical models confirm that combined dietary arginine deprivation, GCN2 inhibition, and senotherapy promote HCC cell apoptosis and tumor regression. These data suggest novel strategies to treat human liver cancers through targeting SLC7A1 and/or a combination of arginine restriction, inhibition of GCN2, and senolytic agents.
Publication Cell Metabolism
Volume 34
Issue 8
Pages 1151-1167.e7
Date 2022-08-02
Journal Abbr Cell Metab
Language eng
DOI 10.1016/j.cmet.2022.06.010
ISSN 1932-7420
Library Catalog PubMed
Extra PMID: 35839757 PMCID: PMC9357184
Tags Arginine, Carcinoma, Hepatocellular, GCN2, hepatocellular carcinoma, Humans, Liver Neoplasms, original, Protein Serine-Threonine Kinases, senescence, Senotherapeutics, urea cycle
Date Added 2024/12/03 - 09:12:56
Date Modified 2024/12/03 - 09:12:56
Notes and Attachments PubMed entry (Attachment)


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