Molecular Mechanisms to Target Cellular Senescence in Hepatocellular Carcinoma.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
25 11 2020
Historique:
received: 03 10 2020
revised: 17 11 2020
accepted: 20 11 2020
entrez: 1 12 2020
pubmed: 2 12 2020
medline: 23 6 2021
Statut: epublish

Résumé

Hepatocellular carcinoma (HCC) has emerged as a major cause of cancer-related death and is the most common type of liver cancer. Due to the current paucity of drugs for HCC therapy there is a pressing need to develop new therapeutic concepts. In recent years, the role of Serum Response Factor (SRF) and its coactivators, Myocardin-Related Transcription Factors A and B (MRTF-A and -B), in HCC formation and progression has received considerable attention. Targeting MRTFs results in HCC growth arrest provoked by oncogene-induced senescence. The induction of senescence acts as a tumor-suppressive mechanism and therefore gains consideration for pharmacological interventions in cancer therapy. In this article, we describe the key features and the functional role of senescence in light of the development of novel drug targets for HCC therapy with a focus on MRTFs.

Identifiants

pubmed: 33255630
pii: cells9122540
doi: 10.3390/cells9122540
pmc: PMC7761055
pii:
doi:

Substances chimiques

Serum Response Factor 0
Transcription Factors 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Constanze Mittermeier (C)

Cancer Science Institute of Singapore, National University of Singapore, Singapore 117599, Singapore.

Andreas Konopa (A)

Department of Chemistry and Pharmacy, Molecular and Clinical Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany.

Susanne Muehlich (S)

Department of Chemistry and Pharmacy, Molecular and Clinical Pharmacy, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany.

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