Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/21627
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dc.contributor.authorZahra, A-
dc.contributor.authorSisu, C-
dc.contributor.authorSilva, E-
dc.contributor.authorDe Aguiar Greca, S-C-
dc.contributor.authorRandeva, H-
dc.contributor.authorChatha, K-
dc.contributor.authorKyrou, I-
dc.contributor.authorKarteris, E-
dc.date.accessioned2020-10-08T10:44:39Z-
dc.date.available2020-10-08T10:44:39Z-
dc.date.issued2020-10-14-
dc.identifier3296-
dc.identifier.citationZahra, A., Sisu, C., Silva, E., De Aguiar Greca, S.-C., Randeva, H. S., Chatha, K., Kyrou, I. and Karteris, E. (2020) ‘Is There a Link between Bisphenol A (BPA), a Key Endocrine Disruptor, and the Risk for SARS-CoV-2 Infection and Severe COVID-19?’, Journal of Clinical Medicine. MDPI AG, 9(10), 3296, pp. 1-15. doi: 10.3390/jcm9103296.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/21627-
dc.description.abstract© 2020 by the authors. Infection by the severe acute respiratory syndrome (SARS) coronavirus-2 (SARS-CoV-2) is the causative agent of a new disease (COVID-19). The risk of severe COVID-19 is increased by certain underlying comorbidities, including asthma, cancer, cardiovascular disease, hypertension, diabetes, and obesity. Notably, exposure to hormonally active chemicals, so called, endocrine disrupting chemicals (EDCs) can promote such cardio-metabolic diseases, endocrine-related cancers, and immune system dysregulation and, thus, may also be linked to higher risk of severe COVID-19. Bisphenol A (BPA) is among the most common EDCs and exerts its effects via receptors which are widely distributed in human tissues, including nuclear estrogen receptors (ERα and ERβ), membrane-bound estrogen receptor GPR30 and human nuclear receptor estrogen-related receptor gamma. As such, this paper focuses on the potential role of BPA in promoting comorbidities associated with severe COVID-19, as well as on potential BPA-induced effects on key SARS-CoV-2 infection mediators, such as angiotensin-converting enzyme 2 (ACE2), and transmembrane serine protease 2 (TMPRSS2). Interestingly, GPR30 appears to exhibit greater co-localisation with TMPRSS2 in key tissues like lung, and prostate, suggesting that BPA exposure may impact on the local expression of these SARS-CoV-2 infection mediators. Overall, the potential role of BPA on the risk and severity of COVID-19 merits further investigation.en_US
dc.description.sponsorshipIsambard Kingdom Brunel Research Scholarshipen_US
dc.description.sponsorshipIsambard Kingdom Brunel Research Scholarship-
dc.format.extent1 - 15-
dc.format.mediumElectronic-
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rights© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectSARS-CoV-2en_US
dc.subjectCOVID-19en_US
dc.subjectBPAen_US
dc.subjectestrogen receptorsen_US
dc.subjectACE2en_US
dc.subjectTMPRSS2en_US
dc.subjectendocrine disruptorsen_US
dc.titleIs there a link between bisphenol A (BPA), a key endocrine disruptor, and the risk for SARS-CoV-2 infection and severe COVID-19?en_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.3390/jcm9103296-
dc.relation.isPartOfJournal of Clinical Medicine-
pubs.issue10-
pubs.publication-statusPublished-
pubs.volume9-
dc.identifier.eissn2077-0383-
Appears in Collections:Dept of Life Sciences Research Papers

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