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How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa
Despite ongoing efforts, sub-Saharan Africa faces a higher cervical cancer burden than anywhere else in the world. Besides HPV infection, definitive factors of cervical cancer are still unclear. Particular states of the cervicovaginal microbiota and viral infections are associated with increased cer...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028704/ https://www.ncbi.nlm.nih.gov/pubmed/32117800 http://dx.doi.org/10.3389/fcimb.2020.00023 |
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author | Klein, Cameron Kahesa, Crispin Mwaiselage, Julius West, John T. Wood, Charles Angeletti, Peter C. |
author_facet | Klein, Cameron Kahesa, Crispin Mwaiselage, Julius West, John T. Wood, Charles Angeletti, Peter C. |
author_sort | Klein, Cameron |
collection | PubMed |
description | Despite ongoing efforts, sub-Saharan Africa faces a higher cervical cancer burden than anywhere else in the world. Besides HPV infection, definitive factors of cervical cancer are still unclear. Particular states of the cervicovaginal microbiota and viral infections are associated with increased cervical cancer risk. Notably, HIV infection, which is prevalent in sub-Saharan Africa, greatly increases risk of cervicovaginal dysbiosis and cervical cancer. To better understand and address cervical cancer in sub-Saharan Africa, a better knowledge of the regional cervicovaginal microbiome is required This review establishes current knowledge of HPV, HIV, cervicovaginal infections, and the cervicovaginal microbiota in sub-Saharan Africa. Because population statistics are not available for the region, estimates are derived from smaller cohort studies. Microbiota associated with cervical inflammation have been found to be especially prevalent in sub-Saharan Africa, and to associate with increased cervical cancer risk. In addition to high prevalence and diversity of HIV and HPV, intracellular bacterial infections such as Chlamydia, Gonorrhea, and Mycoplasma hominis are much more common than in regions with a low burden of cervical cancer. This suggests the prevalence of cervical cancer in sub-Saharan Africa may be partially attributed to increased cervical inflammation resulting from higher likelihood of cervical infection and/or microbial dysbiosis. |
format | Online Article Text |
id | pubmed-7028704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70287042020-02-28 How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa Klein, Cameron Kahesa, Crispin Mwaiselage, Julius West, John T. Wood, Charles Angeletti, Peter C. Front Cell Infect Microbiol Cellular and Infection Microbiology Despite ongoing efforts, sub-Saharan Africa faces a higher cervical cancer burden than anywhere else in the world. Besides HPV infection, definitive factors of cervical cancer are still unclear. Particular states of the cervicovaginal microbiota and viral infections are associated with increased cervical cancer risk. Notably, HIV infection, which is prevalent in sub-Saharan Africa, greatly increases risk of cervicovaginal dysbiosis and cervical cancer. To better understand and address cervical cancer in sub-Saharan Africa, a better knowledge of the regional cervicovaginal microbiome is required This review establishes current knowledge of HPV, HIV, cervicovaginal infections, and the cervicovaginal microbiota in sub-Saharan Africa. Because population statistics are not available for the region, estimates are derived from smaller cohort studies. Microbiota associated with cervical inflammation have been found to be especially prevalent in sub-Saharan Africa, and to associate with increased cervical cancer risk. In addition to high prevalence and diversity of HIV and HPV, intracellular bacterial infections such as Chlamydia, Gonorrhea, and Mycoplasma hominis are much more common than in regions with a low burden of cervical cancer. This suggests the prevalence of cervical cancer in sub-Saharan Africa may be partially attributed to increased cervical inflammation resulting from higher likelihood of cervical infection and/or microbial dysbiosis. Frontiers Media S.A. 2020-02-12 /pmc/articles/PMC7028704/ /pubmed/32117800 http://dx.doi.org/10.3389/fcimb.2020.00023 Text en Copyright © 2020 Klein, Kahesa, Mwaiselage, West, Wood and Angeletti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Klein, Cameron Kahesa, Crispin Mwaiselage, Julius West, John T. Wood, Charles Angeletti, Peter C. How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title | How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title_full | How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title_fullStr | How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title_full_unstemmed | How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title_short | How the Cervical Microbiota Contributes to Cervical Cancer Risk in Sub-Saharan Africa |
title_sort | how the cervical microbiota contributes to cervical cancer risk in sub-saharan africa |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028704/ https://www.ncbi.nlm.nih.gov/pubmed/32117800 http://dx.doi.org/10.3389/fcimb.2020.00023 |
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