Association between the Estrogen receptor β rs1256049 polymorphism and prostate cancer risk:a meta-analysis.


Journal

Annales de biologie clinique
ISSN: 1950-6112
Titre abrégé: Ann Biol Clin (Paris)
Pays: France
ID NLM: 2984690R

Informations de publication

Date de publication:
21 07 2023
Historique:
medline: 24 7 2023
pubmed: 17 6 2023
entrez: 17 6 2023
Statut: ppublish

Résumé

The Estrogen receptor β (ESR-β) gene is suggested to have a growth inhibitory role in prostate tissue and was proposed as a new therapeutic target for prostate cancer (PCa). Precedent studies have investigated the association between the ESR-β rs1256049 polymorphism and PCa but findings were inconsistent. Thus, this meta-analysis was performed to assess whether the ESR-β rs1256049 polymorphism is associated with an increased susceptibility to PCa. Eligible studies published before February 5, 2022 were systematically searched in PubMed, Web of Science, ScienceDirect and Google Scholar databases. The sample set was extracted from 11 case-control studies involving 9390 cases and 10057 controls for the association between ESR-β rs1256049 polymorphism and PCa susceptibility. In our overall meta-analysis, no significant association between rs1256049 and PCa risk was found under all genetic models. In subgroup analysis according to ethnicity, Asians, had a significantly decreased cancer risk based on both the heterozygote genetic model (OR = 0.75, 95% CI = [0.63, 0.89] P = 0.01) and the dominant model (OR = 0.80, 95% CI [0.69, 0.94] P = 0.01). For the Caucasian group, there was a significantly increased risk observed in the allelic model (OR = 1.17, 95% CI = [1.04, 1.32] P = 0.01), heterozygote model (OR = 1.15, 95% CI = [1.01, 1.31] P = 0.03) and the dominant model (OR = 1.17, 95% CI = [1.03, 1.32] P = 0.01). Our results demonstrate that ESR-β r1256049 polymorphism may play a possible promising effect in PCa in Caucasians and a protective factor in Asians.

Identifiants

pubmed: 37329151
pii: abc.2023.1815
doi: 10.1684/abc.2023.1815
doi:

Substances chimiques

Estrogen Receptor beta 0
ESR2 protein, human 0

Types de publication

Systematic Review Meta-Analysis Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

280-288

Auteurs

Hassane Gazzaz (H)

Clinical, metabolic and molecular biochemistry Team, Faculty of Medicine and Pharmacy, Mohammed V University, 10100 Rabat, Morocco, Higher Institute of Nursing Professions and Health Techniques of Marrakech, annex of Safi, Morocco.

Mohammed El Feniche (M)

Laboratory of Biostatistics, Clinical Research and Epidemiology, Faculty of Medicine and Pharmacy, Mohammed V University, 10100 Rabat, Morocco.

Ahmed Ameur (A)

Department of urology, Military Hospital Mohammed V, 10045 Rabat, Morocco.

Abdellah Dami (A)

Clinical, metabolic and molecular biochemistry Team, Faculty of Medicine and Pharmacy, Mohammed V University, 10100 Rabat, Morocco, Department of biochemistry and toxicology, Military Hospital Mohammed V, 10045 Rabat, Morocco.

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Classifications MeSH