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TP53 rs1042522 polymorphism and early-onset breast cancer

BACKGROUND: Breast cancer is the leading cause of cancer deaths among women. Early-onset breast cancer is well recognized as it clinically differs from old-age diagnosed breast neoplasms. TP53 rs1042522 polymorphism relates to the risk of breast neoplasms, but this relationship in Turkish early-onse...

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Autores principales: Icen-Taskin, Irmak, Irtegun-Kandemir, Sevgi, Munzuroglu, Omer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213006/
https://www.ncbi.nlm.nih.gov/pubmed/32419782
http://dx.doi.org/10.4103/jrms.JRMS_506_19
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author Icen-Taskin, Irmak
Irtegun-Kandemir, Sevgi
Munzuroglu, Omer
author_facet Icen-Taskin, Irmak
Irtegun-Kandemir, Sevgi
Munzuroglu, Omer
author_sort Icen-Taskin, Irmak
collection PubMed
description BACKGROUND: Breast cancer is the leading cause of cancer deaths among women. Early-onset breast cancer is well recognized as it clinically differs from old-age diagnosed breast neoplasms. TP53 rs1042522 polymorphism relates to the risk of breast neoplasms, but this relationship in Turkish early-onset breast cancer patients has not been investigated yet. We aimed to search the relationship between TP53 rs1042522 polymorphism and young Turkish breast cancer patients. MATERIALS AND METHODS: Ninety-six female breast cancer patients who were ≤ 40 years of age and 96 healthy controls were enrolled in our study. Participants were genotyped by the hybridization probe system. RESULTS: We identified that the genotype frequencies of rs1042522 were significantly different between controls and cases (P = 0.027). Participants carrying CG genotype had also reduced breast cancer risk (odds ratio = 0.4196, 95% confidence interval: 0.1941–0.9067, P = 0.027). Our results revealed that there is an association between GG and CG + CC genotype groups with progesterone receptor (PgR) status (P = 0.0219). CONCLUSION: Our findings indicate that the CG genotype is a protective factor against breast neoplasms. No other clinicopathologic parameters except for PgR status were found to be related to rs1042522 polymorphism in young Turkish breast cancer patients.
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spelling pubmed-72130062020-05-15 TP53 rs1042522 polymorphism and early-onset breast cancer Icen-Taskin, Irmak Irtegun-Kandemir, Sevgi Munzuroglu, Omer J Res Med Sci Original Article BACKGROUND: Breast cancer is the leading cause of cancer deaths among women. Early-onset breast cancer is well recognized as it clinically differs from old-age diagnosed breast neoplasms. TP53 rs1042522 polymorphism relates to the risk of breast neoplasms, but this relationship in Turkish early-onset breast cancer patients has not been investigated yet. We aimed to search the relationship between TP53 rs1042522 polymorphism and young Turkish breast cancer patients. MATERIALS AND METHODS: Ninety-six female breast cancer patients who were ≤ 40 years of age and 96 healthy controls were enrolled in our study. Participants were genotyped by the hybridization probe system. RESULTS: We identified that the genotype frequencies of rs1042522 were significantly different between controls and cases (P = 0.027). Participants carrying CG genotype had also reduced breast cancer risk (odds ratio = 0.4196, 95% confidence interval: 0.1941–0.9067, P = 0.027). Our results revealed that there is an association between GG and CG + CC genotype groups with progesterone receptor (PgR) status (P = 0.0219). CONCLUSION: Our findings indicate that the CG genotype is a protective factor against breast neoplasms. No other clinicopathologic parameters except for PgR status were found to be related to rs1042522 polymorphism in young Turkish breast cancer patients. Wolters Kluwer - Medknow 2020-03-18 /pmc/articles/PMC7213006/ /pubmed/32419782 http://dx.doi.org/10.4103/jrms.JRMS_506_19 Text en Copyright: © 2020 Journal of Research in Medical Sciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Icen-Taskin, Irmak
Irtegun-Kandemir, Sevgi
Munzuroglu, Omer
TP53 rs1042522 polymorphism and early-onset breast cancer
title TP53 rs1042522 polymorphism and early-onset breast cancer
title_full TP53 rs1042522 polymorphism and early-onset breast cancer
title_fullStr TP53 rs1042522 polymorphism and early-onset breast cancer
title_full_unstemmed TP53 rs1042522 polymorphism and early-onset breast cancer
title_short TP53 rs1042522 polymorphism and early-onset breast cancer
title_sort tp53 rs1042522 polymorphism and early-onset breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213006/
https://www.ncbi.nlm.nih.gov/pubmed/32419782
http://dx.doi.org/10.4103/jrms.JRMS_506_19
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