Evidence map›Paper›PMID 41459848›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Association of miR-126 and miR-143/145 Gene Polymorphisms with the Risk and Clinicopathological Features of Prostate Cancer.

Gholamreza Bahari, Nahid Rahimi, Mohammad Hashemi, Mohammad Amin Siri, Behzad Narouie

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Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Gholamreza BahariDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Nahid RahimiDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Mohammad HashemiDepartment of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.
Mohammad Amin SiriSchool of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Behzad NarouieDepartment of Urology, Zahedan University of Medical Sciences, Zahedan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) represents a significant cause of morbidity and mortality among men. Recently, several biomarkers have been introduced to address the shortcomings in PCa management, including screening and diagnosis. MicroRNAs (miRNAs) are relatively novel biomarkers that may be dysregulated in PCa. However, the knowledge regarding the association between miRNA dysregulations and PCa remains limited in Iran.

methodsWe performed a case-control analysis, comparing miR-126 rs4636297, miR-143/145 rs353292, miR-143/145 rs4705342, and miR-143/145 rs4705343 polymorphisms in 185 PCa patients and 220 cancer-free men based on DNA extracted from blood samples of Iranian subjects. Moreover, the correlation between clinicopathological features of PCa and these polymorphisms was  investigated.

resultsmiR-126 rs4636297 A>G, miR-143/145 rs353292 C>T, and miR-143/145 rs4705343 T>C variants were associated with a reduced risk of PCa in codominant, dominant, recessive, and allelic inheritance models. With the exception of the recessive inheritance pattern, the miR-143/145 rs4705342 T>C variant was also correlated with a reduced risk of PCa. Additionally, haplotype analysis of miR-143/145 (rs353292, rs4705342, and rs4705343, respectively) polymorphisms revealed that the CTT haplotype was the most frequent in cases and controls. Moreover, CTC, TTT, TCC, and TCT were associated with decreased risk of PCa. Finally, no relationship was identified between certain clinicopathological aspects of PCa and the mentioned polymorphisms.

conclusionsWe identified several miR polymorphisms and distinct haplotypes associated with reduced PCa risk in a sample of the Iranian population. These findings pave the way for optimized PCa management and provide a better understanding of its pathophysiology.

Indexed as

Biomarkers, TumorGenetic Predisposition to DiseaseMicroRNAsPolymorphism, Single NucleotideProstatic NeoplasmsAgedCase-Control StudiesFollow-Up StudiesGenotypeHumansIranMaleMiddle AgedPrognosisRisk FactorsBiomarkers, TumorMicroRNAsMIRN126 microRNA, humanMIRN143 microRNA, humanMIRN145 microRNA, humanMicroRNAsmiR-126miR-143/145PolymorphismProstatic Neoplasms

Identifiers

PMID41459848
PMCPMC13236074

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