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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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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. |
format | Online Article Text |
id | pubmed-7213006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
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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