Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies
Single nucleotide polymorphisms (SNPs) are the most common type of genetic variation among people. Genome Wide Association studies (GWASs) have generated multiple genetic variants associated with prostate cancer (PC) risk. Taking into account previously identified genetic susceptibility variants, th...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-10-01
|
Series: | Biomedicines |
Subjects: | |
Online Access: | https://www.mdpi.com/2227-9059/10/11/2733 |
_version_ | 1797468970809294848 |
---|---|
author | Anca Gabriela Pavel Danae Stambouli Gabriela Anton Ismail Gener Adrian Preda Catalin Baston Constantin Gingu |
author_facet | Anca Gabriela Pavel Danae Stambouli Gabriela Anton Ismail Gener Adrian Preda Catalin Baston Constantin Gingu |
author_sort | Anca Gabriela Pavel |
collection | DOAJ |
description | Single nucleotide polymorphisms (SNPs) are the most common type of genetic variation among people. Genome Wide Association studies (GWASs) have generated multiple genetic variants associated with prostate cancer (PC) risk. Taking into account previously identified genetic susceptibility variants, the purpose of our study was to determine the cumulative association between four common SNPs and the overall PC risk. A total of 78 specimens from both PC and benign prostate hyperplasia (BPH) patients were included in the study. Genotyping of all selected SNPs was performed using the TaqMan assay. The association between each SNP and the PC risk was assessed individually and collectively. Analysis of the association between individual SNPs and PC risk revealed that only the rs4054823 polymorphism was significantly associated with PC, and not with BPH (<i>p</i> < 0.001). Statistical analysis also showed that the heterozygous genotype of the rs2735839 polymorphism is more common within the BPH group than in the PC group (<i>p</i> = 0.042). The cumulative effect of high-risk alleles on PC was analyzed using a logistic regression model. As a result, the carriers of at least one risk allele copy in each particular region had a cumulative odd ratio (OR) of 1.42 times, compared to subjects who did not have any of these factors. In addition, the combination of these four genetic variants increased the overall risk of PC by 52%. Our study provides further evidence of the cumulative effects of genetic risk factors on overall PC risk. These results should encourage future research to explain the interactions between known susceptibility variants and their contribution to the development and progression of PC disease. |
first_indexed | 2024-03-09T19:14:52Z |
format | Article |
id | doaj.art-1c6710856633470cb698374aa0cb3cc6 |
institution | Directory Open Access Journal |
issn | 2227-9059 |
language | English |
last_indexed | 2024-03-09T19:14:52Z |
publishDate | 2022-10-01 |
publisher | MDPI AG |
record_format | Article |
series | Biomedicines |
spelling | doaj.art-1c6710856633470cb698374aa0cb3cc62023-11-24T03:49:49ZengMDPI AGBiomedicines2227-90592022-10-011011273310.3390/biomedicines10112733Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary StudiesAnca Gabriela Pavel0Danae Stambouli1Gabriela Anton2Ismail Gener3Adrian Preda4Catalin Baston5Constantin Gingu6Cytogenomic Medical Laboratory, Molecular Genetics Department, 014453 Bucharest, RomaniaCytogenomic Medical Laboratory, Molecular Genetics Department, 014453 Bucharest, RomaniaThe Romania Academy, “Stefan S. Nicolau” Institute of Virology, 030304 Bucharest, RomaniaDepartment of Nephrology, Urology, Immunology and Immunology of Transplant, Dermatology, Allergology, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, 010751 Bucharest, RomaniaCenter of Urological Surgery, Dialysis and Renal Transplantation, Fundeni Clinical Institute, 022328 Bucharest, RomaniaDepartment of Nephrology, Urology, Immunology and Immunology of Transplant, Dermatology, Allergology, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, 010751 Bucharest, RomaniaDepartment of Nephrology, Urology, Immunology and Immunology of Transplant, Dermatology, Allergology, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, 010751 Bucharest, RomaniaSingle nucleotide polymorphisms (SNPs) are the most common type of genetic variation among people. Genome Wide Association studies (GWASs) have generated multiple genetic variants associated with prostate cancer (PC) risk. Taking into account previously identified genetic susceptibility variants, the purpose of our study was to determine the cumulative association between four common SNPs and the overall PC risk. A total of 78 specimens from both PC and benign prostate hyperplasia (BPH) patients were included in the study. Genotyping of all selected SNPs was performed using the TaqMan assay. The association between each SNP and the PC risk was assessed individually and collectively. Analysis of the association between individual SNPs and PC risk revealed that only the rs4054823 polymorphism was significantly associated with PC, and not with BPH (<i>p</i> < 0.001). Statistical analysis also showed that the heterozygous genotype of the rs2735839 polymorphism is more common within the BPH group than in the PC group (<i>p</i> = 0.042). The cumulative effect of high-risk alleles on PC was analyzed using a logistic regression model. As a result, the carriers of at least one risk allele copy in each particular region had a cumulative odd ratio (OR) of 1.42 times, compared to subjects who did not have any of these factors. In addition, the combination of these four genetic variants increased the overall risk of PC by 52%. Our study provides further evidence of the cumulative effects of genetic risk factors on overall PC risk. These results should encourage future research to explain the interactions between known susceptibility variants and their contribution to the development and progression of PC disease.https://www.mdpi.com/2227-9059/10/11/2733polymorphismprostate cancercumulative effectgenetic riskgenotyping |
spellingShingle | Anca Gabriela Pavel Danae Stambouli Gabriela Anton Ismail Gener Adrian Preda Catalin Baston Constantin Gingu Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies Biomedicines polymorphism prostate cancer cumulative effect genetic risk genotyping |
title | Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies |
title_full | Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies |
title_fullStr | Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies |
title_full_unstemmed | Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies |
title_short | Cumulative Effect Assessment of Common Genetic Variants on Prostate Cancer: Preliminary Studies |
title_sort | cumulative effect assessment of common genetic variants on prostate cancer preliminary studies |
topic | polymorphism prostate cancer cumulative effect genetic risk genotyping |
url | https://www.mdpi.com/2227-9059/10/11/2733 |
work_keys_str_mv | AT ancagabrielapavel cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT danaestambouli cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT gabrielaanton cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT ismailgener cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT adrianpreda cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT catalinbaston cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies AT constantingingu cumulativeeffectassessmentofcommongeneticvariantsonprostatecancerpreliminarystudies |