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Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females
BACKGROUND: Epstein-Barr virus (EBV) has been implicated in the development of breast cancer (BC) since 1995. It is classified into A/B genotypes, C/D subtypes, and F/f variants according to variations in its genome. AIM: To determine the distribution difference of EBV types between BC patients and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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West Asia Organization for Cancer Prevention
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272632/ https://www.ncbi.nlm.nih.gov/pubmed/35225477 http://dx.doi.org/10.31557/APJCP.2022.23.2.641 |
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author | Mashaly, Mervat Ghorab, Doaa Hegazy, Mohamed Abdelkhalek, Mohamed Gaballa, Khaled Elzehery, Rasha |
author_facet | Mashaly, Mervat Ghorab, Doaa Hegazy, Mohamed Abdelkhalek, Mohamed Gaballa, Khaled Elzehery, Rasha |
author_sort | Mashaly, Mervat |
collection | PubMed |
description | BACKGROUND: Epstein-Barr virus (EBV) has been implicated in the development of breast cancer (BC) since 1995. It is classified into A/B genotypes, C/D subtypes, and F/f variants according to variations in its genome. AIM: To determine the distribution difference of EBV types between BC patients and healthy controls in Egypt and to detect the association between different EBV types and BC characteristics. METHODS: Three hundred and sixty-two participants (142 BC patients and 220 controls) were enrolled in this study. All participants were screened for EBV infection by determination of viral-capsid-IgG antibodies in their sera. EBNA-1 gene was detected by PCR in tumor biopsies of seropositive patients and in peripheral blood mononuclear cells of controls. A/B genotyping of EBV was performed by nested-PCR targeting the EBNA-2 gene. C/D subtypes and F/f variants were identified by Restriction fragment length polymorphism at BamHI-I W1/I1 and BamHI-F regions of EBV genome, respectively. RESULTS: Among 362 participants, 300(82.9%) were EBV-seropositive, including 120/142(84.5%) of the BC patients and 180/220(81.8 %) of the controls. EBNA-1 gene was positive in 54(45%) of seropositive BC patients and in 38(21.1%) of seropositive controls. There was a significant association of EBNA-1 gene with breast cancer (OR=3.05, 95%CI=1.84-5.07). Moreover, EBNA-1 gene positivity was significantly associated with the more aggressive tumors. Genotype-A and prototype-F were predominant among patients (90.4%, 100%, respectively) as well as among controls (91.7%, 100%, respectively) with no statistical significant association with BC risk. However, subtype-D was significantly more frequent in patients (95.6%) than in controls (64.7%) and was significantly associated with a higher BC risk as compared to subtype-C (OR=11.7, 95%CI=2.4-57.08). Subtype-D was significantly associated with higher grades tumors (100% among grade III), with progesteron receptor-negative tumors and with HER2-positive tumors (100% for each). The combined genotypes that significantly associated with BC risk were ADF (OR=4.9) and BDF (OR=5.5). CONCLUSIONS: Subtype-D of EBV could be the only EBV type implicated in BC development among Egyptian females and associated more with poor prognosis. |
format | Online Article Text |
id | pubmed-9272632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | West Asia Organization for Cancer Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-92726322022-07-14 Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females Mashaly, Mervat Ghorab, Doaa Hegazy, Mohamed Abdelkhalek, Mohamed Gaballa, Khaled Elzehery, Rasha Asian Pac J Cancer Prev Research Article BACKGROUND: Epstein-Barr virus (EBV) has been implicated in the development of breast cancer (BC) since 1995. It is classified into A/B genotypes, C/D subtypes, and F/f variants according to variations in its genome. AIM: To determine the distribution difference of EBV types between BC patients and healthy controls in Egypt and to detect the association between different EBV types and BC characteristics. METHODS: Three hundred and sixty-two participants (142 BC patients and 220 controls) were enrolled in this study. All participants were screened for EBV infection by determination of viral-capsid-IgG antibodies in their sera. EBNA-1 gene was detected by PCR in tumor biopsies of seropositive patients and in peripheral blood mononuclear cells of controls. A/B genotyping of EBV was performed by nested-PCR targeting the EBNA-2 gene. C/D subtypes and F/f variants were identified by Restriction fragment length polymorphism at BamHI-I W1/I1 and BamHI-F regions of EBV genome, respectively. RESULTS: Among 362 participants, 300(82.9%) were EBV-seropositive, including 120/142(84.5%) of the BC patients and 180/220(81.8 %) of the controls. EBNA-1 gene was positive in 54(45%) of seropositive BC patients and in 38(21.1%) of seropositive controls. There was a significant association of EBNA-1 gene with breast cancer (OR=3.05, 95%CI=1.84-5.07). Moreover, EBNA-1 gene positivity was significantly associated with the more aggressive tumors. Genotype-A and prototype-F were predominant among patients (90.4%, 100%, respectively) as well as among controls (91.7%, 100%, respectively) with no statistical significant association with BC risk. However, subtype-D was significantly more frequent in patients (95.6%) than in controls (64.7%) and was significantly associated with a higher BC risk as compared to subtype-C (OR=11.7, 95%CI=2.4-57.08). Subtype-D was significantly associated with higher grades tumors (100% among grade III), with progesteron receptor-negative tumors and with HER2-positive tumors (100% for each). The combined genotypes that significantly associated with BC risk were ADF (OR=4.9) and BDF (OR=5.5). CONCLUSIONS: Subtype-D of EBV could be the only EBV type implicated in BC development among Egyptian females and associated more with poor prognosis. West Asia Organization for Cancer Prevention 2022-02 /pmc/articles/PMC9272632/ /pubmed/35225477 http://dx.doi.org/10.31557/APJCP.2022.23.2.641 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License. https://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Research Article Mashaly, Mervat Ghorab, Doaa Hegazy, Mohamed Abdelkhalek, Mohamed Gaballa, Khaled Elzehery, Rasha Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title | Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title_full | Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title_fullStr | Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title_full_unstemmed | Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title_short | Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females |
title_sort | association between epstein-barr virus gene polymorphism and breast cancer risk among egyptian females |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272632/ https://www.ncbi.nlm.nih.gov/pubmed/35225477 http://dx.doi.org/10.31557/APJCP.2022.23.2.641 |
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