Cancer prevalence after exposure to Wnt-activating drugs: a systematic review.
systematic_review · Level I
Where this comes from
- Record sourced from PubMed, PMID 40447428.
- Also identified by DOI 10.1136/bmjopen-2025-103296 and PMC identifier 12142115.
- Licence recorded as CC BY-NC.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
To assess whether treatment with drugs that activate the Wnt pathway leads to an increased risk of cancer. Systematic review reported using Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) reporting guidelines. PubMed, Embase and the Cochrane Library were searched through 1 November 2024. All primary research articles reporting clinical studies, including observational and experimental studies, were included in this review. All studies were eligible for inclusion if they included the exposure of interest, that is, compounds which have been described to activate the Wnt pathway, and the outcome of interest, that is, cancer prevalence. No language restrictions were performed. This study was reported according to the PRISMA reporting guidelines. The search string, objectives, and study protocol methods were defined before the study was initiated. A total of 48 studies investigating drugs that activate the Wnt pathway (valproic acid, lithium, cimetidine, olanzapine, clozapine, haloperidol) were included in this systematic review. The results from this systematic review show that, at least for the included compounds in the currently used systemic dosage, cancer prevalence does not significantly increase. The current study found that the use of drugs that activate the Wnt pathway was not associated with an increased risk of cancer. As a promising agent in the regenerative therapy field, further research into Wnt activation as a treatment option should be explored. CRD42021286193.
Medical subject headings
- Neoplasms
- Wnt Signaling Pathway