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Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women

BACKGROUND: Breast cancer is the leading cause of mortality among women, with over a million cases recorded globally. Haptoglobin (Hp) protein and genotypes play important roles in cancer predisposition and progression, but studies have reported varying outcomes in populations. AIM: The association...

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Autores principales: Dokunmu, Titilope M., Obi, Patience O., Fatiregun, Omolara A., Rotimi, Oluwakemi A., Agodirin, Sulaiman O., Rotimi, Solomon O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671171/
https://www.ncbi.nlm.nih.gov/pubmed/36204908
http://dx.doi.org/10.4103/1596-3519.356811
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author Dokunmu, Titilope M.
Obi, Patience O.
Fatiregun, Omolara A.
Rotimi, Oluwakemi A.
Agodirin, Sulaiman O.
Rotimi, Solomon O.
author_facet Dokunmu, Titilope M.
Obi, Patience O.
Fatiregun, Omolara A.
Rotimi, Oluwakemi A.
Agodirin, Sulaiman O.
Rotimi, Solomon O.
author_sort Dokunmu, Titilope M.
collection PubMed
description BACKGROUND: Breast cancer is the leading cause of mortality among women, with over a million cases recorded globally. Haptoglobin (Hp) protein and genotypes play important roles in cancer predisposition and progression, but studies have reported varying outcomes in populations. AIM: The association of Hp genotypes in breast cancer patients with malaria has not been investigated in Nigerians, which is the aim of our study. In healthy women (control; n = 279) and clinically diagnosed breast cancer patients (breast cancer; n = 70). METHODS: Haptoglobin genotypes and Plasmodium falciparum cyclooxygenase III genes were detected by polymerase chain reaction (PCR). Proportions were compared, and the test of association was carried out with a significance level set at P < 0.05. RESULTS: Overall, 311 of 349 (89%) individuals had malaria infection with similar proportions in breast cancer (63 of 70) and healthy control group (248 of 279); malaria incidence was, however, lower in Hp 2-2 breast cancer patients (P = 0.04). The prevalence of Hp genotypes was Hp 1-1 (78.2%), Hp 2-1 (7.2%), and 2-2 (14.6%). In breast cancer groups, Hp 2-2 genotype was significantly lower with 3 (4.2%) of 70 vs. 48 (17.2%) of 279 in control group (P = 0.006). CONCLUSIONS: The results of the study show low Hp 2-2 genotype relative to other genotypes in breast cancer patients; we conclude that low Hp 2-2 genotype is associated with lower malaria risk in breast cancer Nigerian women. It is important to further understand the roles malaria, Hp, and other genotypes play in the pathogenesis of aggressive breast cancer commonly seen in Nigerian women.
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spelling pubmed-96711712022-11-18 Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women Dokunmu, Titilope M. Obi, Patience O. Fatiregun, Omolara A. Rotimi, Oluwakemi A. Agodirin, Sulaiman O. Rotimi, Solomon O. Ann Afr Med Original Article BACKGROUND: Breast cancer is the leading cause of mortality among women, with over a million cases recorded globally. Haptoglobin (Hp) protein and genotypes play important roles in cancer predisposition and progression, but studies have reported varying outcomes in populations. AIM: The association of Hp genotypes in breast cancer patients with malaria has not been investigated in Nigerians, which is the aim of our study. In healthy women (control; n = 279) and clinically diagnosed breast cancer patients (breast cancer; n = 70). METHODS: Haptoglobin genotypes and Plasmodium falciparum cyclooxygenase III genes were detected by polymerase chain reaction (PCR). Proportions were compared, and the test of association was carried out with a significance level set at P < 0.05. RESULTS: Overall, 311 of 349 (89%) individuals had malaria infection with similar proportions in breast cancer (63 of 70) and healthy control group (248 of 279); malaria incidence was, however, lower in Hp 2-2 breast cancer patients (P = 0.04). The prevalence of Hp genotypes was Hp 1-1 (78.2%), Hp 2-1 (7.2%), and 2-2 (14.6%). In breast cancer groups, Hp 2-2 genotype was significantly lower with 3 (4.2%) of 70 vs. 48 (17.2%) of 279 in control group (P = 0.006). CONCLUSIONS: The results of the study show low Hp 2-2 genotype relative to other genotypes in breast cancer patients; we conclude that low Hp 2-2 genotype is associated with lower malaria risk in breast cancer Nigerian women. It is important to further understand the roles malaria, Hp, and other genotypes play in the pathogenesis of aggressive breast cancer commonly seen in Nigerian women. Wolters Kluwer - Medknow 2022 2022-09-26 /pmc/articles/PMC9671171/ /pubmed/36204908 http://dx.doi.org/10.4103/1596-3519.356811 Text en Copyright: © 2022 Annals of African Medicine https://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
Dokunmu, Titilope M.
Obi, Patience O.
Fatiregun, Omolara A.
Rotimi, Oluwakemi A.
Agodirin, Sulaiman O.
Rotimi, Solomon O.
Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title_full Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title_fullStr Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title_full_unstemmed Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title_short Haptoglobin Genotypes and Malaria Comorbidity in Breast Cancer and Healthy Nigerian Women
title_sort haptoglobin genotypes and malaria comorbidity in breast cancer and healthy nigerian women
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671171/
https://www.ncbi.nlm.nih.gov/pubmed/36204908
http://dx.doi.org/10.4103/1596-3519.356811
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