Emerging role for the Serum Response Factor (SRF) as a potential therapeutic target in cancer.
CCGs compounds
SRF-inhibitors
Serum Response Factor (SRF)
cancer progression
co-factors and co-regulators
hallmarks of cancer
lestaurtinib
novel therapeutics
prognostic biomarker
transcription factors
Journal
Expert opinion on therapeutic targets
ISSN: 1744-7631
Titre abrégé: Expert Opin Ther Targets
Pays: England
ID NLM: 101127833
Informations de publication
Date de publication:
02 2022
02 2022
Historique:
pubmed:
4
2
2022
medline:
3
3
2022
entrez:
3
2
2022
Statut:
ppublish
Résumé
The Serum Response Factor (SRF) is a transcription factor involved in three hallmarks of cancer: the promotion of cell proliferation, cell death resistance and invasion and metastasis induction. Many studies have demonstrated a leading role in the development and progression of multiple cancer types, thus highlighting the potential of SRF as a prognostic biomarker and therapeutic target, especially for cancers with poor prognosis. This review examines the role of SRF in several cancers in promoting cellular processes associated with cancer development and progression. SRF co-factors and signaling pathways are discussed as possible targets to inhibit SRF in a tissue and cancer-specific way. Small-molecule inhibitors of SRF, such as the CCGs series of compounds and lestaurtinib, which could be used as cancer therapeutics, are also discussed. Targeting of SRF and its co-factors represents a promising therapeutic approach. Further understanding of the molecular mechanisms behind the action of SRF could provide a pipeline of novel molecular targets and therapeutic combinations for cancer. Basket clinical trials and the use of SRF immunohistochemistry as companion diagnostics will help testing of these new targets in patients.
Identifiants
pubmed: 35114091
doi: 10.1080/14728222.2022.2032652
doi:
Substances chimiques
Serum Response Factor
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM