The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer

BACKGROUND AND OBJECTIVE: Breast cancer is the most common cancer in women and the leading cause of cancer death in women worldwide. The ERBB4 gene, a member of the tyrosine kinase family, has been identified as both a tumor suppressor and an oncogene in breast cancer. In this study, the association...

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Autores principales: M Zorriye Mahmoud, S Ghaffarian, M Valipour, N Pouladi, V Montazeri
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Publicado: Babol University of Medical Sciences 2021
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spelling oai:doaj.org-article:2e7b1c9b613542db9a7797defc9e0f822021-11-29T07:40:50ZThe Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer1561-41072251-7170https://doaj.org/article/2e7b1c9b613542db9a7797defc9e0f822021-03-01T00:00:00Zhttp://jbums.org/article-1-9922-en.htmlhttps://doaj.org/toc/1561-4107https://doaj.org/toc/2251-7170BACKGROUND AND OBJECTIVE: Breast cancer is the most common cancer in women and the leading cause of cancer death in women worldwide. The ERBB4 gene, a member of the tyrosine kinase family, has been identified as both a tumor suppressor and an oncogene in breast cancer. In this study, the association between rs1972820G>A polymorphism of ERBB4 gene and the risk of breast cancer in northwestern Iran was investigated. METHODS: This case-control study was performed on 89 women with breast cancer and 98 healthy women with no family history of cancer. Clinical characteristics of patients included age (less than, greater than or equal to 49 years and unknown), involved side (right, left, both and unknown), type of tumor (ILC, IDC, other types and unknown), tumor grade (I, II or III), tumor size (T1, T2, T3 and unknown) and lymph node involvement (N0, N1, N2, N3 and unknown). Single nucleotide polymorphisms were examined by TETRA-ARMS-PCR technique. FINDINGS: The genotypic distribution of sick and healthy individuals was 66% and 56% for AA genotype, 9% and 6% for GG genotype and 25% and 38% for AG genotype, respectively. The frequency of Allele A was 147 and 140 and the frequency of G Allele was 49 and 38 in patients and controls, respectively (p>0.05). CONCLUSION: The findings of this study showed that there is no significant relationship between genotypic and allelic distribution of rs1972820 polymorphism of ERBB4 gene with increased risk of breast cancer and clinical features of patients in northwestern Iran.M Zorriye MahmoudS GhaffarianM ValipourN PouladiV MontazeriBabol University of Medical Sciencesarticlebreast cancersingle nucleotide polymorphismassociation evaluationerbb4 gene.MedicineRMedicine (General)R5-920ENFAMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 23, Iss 1, Pp 386-392 (2021)
institution DOAJ
collection DOAJ
language EN
FA
topic breast cancer
single nucleotide polymorphism
association evaluation
erbb4 gene.
Medicine
R
Medicine (General)
R5-920
spellingShingle breast cancer
single nucleotide polymorphism
association evaluation
erbb4 gene.
Medicine
R
Medicine (General)
R5-920
M Zorriye Mahmoud
S Ghaffarian
M Valipour
N Pouladi
V Montazeri
The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
description BACKGROUND AND OBJECTIVE: Breast cancer is the most common cancer in women and the leading cause of cancer death in women worldwide. The ERBB4 gene, a member of the tyrosine kinase family, has been identified as both a tumor suppressor and an oncogene in breast cancer. In this study, the association between rs1972820G>A polymorphism of ERBB4 gene and the risk of breast cancer in northwestern Iran was investigated. METHODS: This case-control study was performed on 89 women with breast cancer and 98 healthy women with no family history of cancer. Clinical characteristics of patients included age (less than, greater than or equal to 49 years and unknown), involved side (right, left, both and unknown), type of tumor (ILC, IDC, other types and unknown), tumor grade (I, II or III), tumor size (T1, T2, T3 and unknown) and lymph node involvement (N0, N1, N2, N3 and unknown). Single nucleotide polymorphisms were examined by TETRA-ARMS-PCR technique. FINDINGS: The genotypic distribution of sick and healthy individuals was 66% and 56% for AA genotype, 9% and 6% for GG genotype and 25% and 38% for AG genotype, respectively. The frequency of Allele A was 147 and 140 and the frequency of G Allele was 49 and 38 in patients and controls, respectively (p>0.05). CONCLUSION: The findings of this study showed that there is no significant relationship between genotypic and allelic distribution of rs1972820 polymorphism of ERBB4 gene with increased risk of breast cancer and clinical features of patients in northwestern Iran.
format article
author M Zorriye Mahmoud
S Ghaffarian
M Valipour
N Pouladi
V Montazeri
author_facet M Zorriye Mahmoud
S Ghaffarian
M Valipour
N Pouladi
V Montazeri
author_sort M Zorriye Mahmoud
title The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
title_short The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
title_full The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
title_fullStr The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
title_full_unstemmed The Association between ERBB4 Gene Polymorphism (SNP: Rs1972820g>A) and the Risk of Breast Cancer
title_sort association between erbb4 gene polymorphism (snp: rs1972820g>a) and the risk of breast cancer
publisher Babol University of Medical Sciences
publishDate 2021
url https://doaj.org/article/2e7b1c9b613542db9a7797defc9e0f82
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