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No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients

BACKGROUND: Cytochrome P450 (CYP)19A1 encodes aromatase, the enzyme responsible for the conversion of androgens to estrogens, and may play a role in variation in outcomes among women with breast cancer. The aim of this study was to analyze the genetic association of rs4646 (A > C) and rs700518 (V...

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Autores principales: Alanazi, Mohammed, Alabdulkarim, Huda A, Shaik, Jilani P, Al Naeem, Abdulrahman, Elrobh, Mohammad, Al Amri, Abdullah, al-Mukaynizi, Fatimah Basil, Semlali, Abdelhabib, Warsy, Arjumand, Parine, Narasimha Reddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567226/
https://www.ncbi.nlm.nih.gov/pubmed/26379441
http://dx.doi.org/10.2147/OTT.S84696
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author Alanazi, Mohammed
Alabdulkarim, Huda A
Shaik, Jilani P
Al Naeem, Abdulrahman
Elrobh, Mohammad
Al Amri, Abdullah
al-Mukaynizi, Fatimah Basil
Semlali, Abdelhabib
Warsy, Arjumand
Parine, Narasimha Reddy
author_facet Alanazi, Mohammed
Alabdulkarim, Huda A
Shaik, Jilani P
Al Naeem, Abdulrahman
Elrobh, Mohammad
Al Amri, Abdullah
al-Mukaynizi, Fatimah Basil
Semlali, Abdelhabib
Warsy, Arjumand
Parine, Narasimha Reddy
author_sort Alanazi, Mohammed
collection PubMed
description BACKGROUND: Cytochrome P450 (CYP)19A1 encodes aromatase, the enzyme responsible for the conversion of androgens to estrogens, and may play a role in variation in outcomes among women with breast cancer. The aim of this study was to analyze the genetic association of rs4646 (A > C) and rs700518 (Val > Val) in the CYP19A1 gene with the risk of breast cancer. METHODS: These two single nucleotide polymorphisms (SNPs) were analyzed in a primary study group of breast cancer patients and healthy control subjects. Genotypes were determined by the TaqMan SNP analysis technique. The study data were analyzed using the chi-square or t-test and logistic regression analysis by Statistical Package for the Social Sciences version 16 software. RESULTS: rs4646 and rs700518 had no association with susceptibility to breast cancer. There was no significant association for either of these SNPs overall in breast cancer samples when compared with healthy control samples. Our data do not support a relationship between the CYP19A1 rs4646 and rs700518 SNPs and risk of breast cancer. It may be that there are ethnic differences with regard to this relationship. CONCLUSION: This study demonstrated that CYP19A1 rs4646 and rs700518 SNPs may not be involved in the etiology of breast cancer in the Saudi population. Confirmation of our findings in larger populations of other ethnicities could provide evidence for the role of the CYP19A1 gene in breast carcinomas.
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spelling pubmed-45672262015-09-14 No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients Alanazi, Mohammed Alabdulkarim, Huda A Shaik, Jilani P Al Naeem, Abdulrahman Elrobh, Mohammad Al Amri, Abdullah al-Mukaynizi, Fatimah Basil Semlali, Abdelhabib Warsy, Arjumand Parine, Narasimha Reddy Onco Targets Ther Original Research BACKGROUND: Cytochrome P450 (CYP)19A1 encodes aromatase, the enzyme responsible for the conversion of androgens to estrogens, and may play a role in variation in outcomes among women with breast cancer. The aim of this study was to analyze the genetic association of rs4646 (A > C) and rs700518 (Val > Val) in the CYP19A1 gene with the risk of breast cancer. METHODS: These two single nucleotide polymorphisms (SNPs) were analyzed in a primary study group of breast cancer patients and healthy control subjects. Genotypes were determined by the TaqMan SNP analysis technique. The study data were analyzed using the chi-square or t-test and logistic regression analysis by Statistical Package for the Social Sciences version 16 software. RESULTS: rs4646 and rs700518 had no association with susceptibility to breast cancer. There was no significant association for either of these SNPs overall in breast cancer samples when compared with healthy control samples. Our data do not support a relationship between the CYP19A1 rs4646 and rs700518 SNPs and risk of breast cancer. It may be that there are ethnic differences with regard to this relationship. CONCLUSION: This study demonstrated that CYP19A1 rs4646 and rs700518 SNPs may not be involved in the etiology of breast cancer in the Saudi population. Confirmation of our findings in larger populations of other ethnicities could provide evidence for the role of the CYP19A1 gene in breast carcinomas. Dove Medical Press 2015-09-03 /pmc/articles/PMC4567226/ /pubmed/26379441 http://dx.doi.org/10.2147/OTT.S84696 Text en © 2015 Alanazi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Alanazi, Mohammed
Alabdulkarim, Huda A
Shaik, Jilani P
Al Naeem, Abdulrahman
Elrobh, Mohammad
Al Amri, Abdullah
al-Mukaynizi, Fatimah Basil
Semlali, Abdelhabib
Warsy, Arjumand
Parine, Narasimha Reddy
No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title_full No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title_fullStr No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title_full_unstemmed No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title_short No associations between aromatase gene polymorphisms and breast cancer risk in Saudi patients
title_sort no associations between aromatase gene polymorphisms and breast cancer risk in saudi patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4567226/
https://www.ncbi.nlm.nih.gov/pubmed/26379441
http://dx.doi.org/10.2147/OTT.S84696
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