Cargando…

ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19

Patients who died from COVID-19 often had comorbidities, such as hypertension, diabetes, and chronic obstructive lung disease. Although angiotensin-converting enzyme 2 (ACE2) is crucial for SARS-CoV2 to bind and enter host cells, no study has systematically assessed the ACE2 expression in the lungs...

Descripción completa

Detalles Bibliográficos
Autores principales: Pinto, Bruna G G, Oliveira, Antonio E R, Singh, Youvika, Jimenez, Leandro, Gonçalves, Andre N A, Ogava, Rodrigo L T, Creighton, Rachel, Peron, Jean Pierre Schatzmann, Nakaya, Helder I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377288/
https://www.ncbi.nlm.nih.gov/pubmed/32526012
http://dx.doi.org/10.1093/infdis/jiaa332
_version_ 1783562189337001984
author Pinto, Bruna G G
Oliveira, Antonio E R
Singh, Youvika
Jimenez, Leandro
Gonçalves, Andre N A
Ogava, Rodrigo L T
Creighton, Rachel
Peron, Jean Pierre Schatzmann
Nakaya, Helder I
author_facet Pinto, Bruna G G
Oliveira, Antonio E R
Singh, Youvika
Jimenez, Leandro
Gonçalves, Andre N A
Ogava, Rodrigo L T
Creighton, Rachel
Peron, Jean Pierre Schatzmann
Nakaya, Helder I
author_sort Pinto, Bruna G G
collection PubMed
description Patients who died from COVID-19 often had comorbidities, such as hypertension, diabetes, and chronic obstructive lung disease. Although angiotensin-converting enzyme 2 (ACE2) is crucial for SARS-CoV2 to bind and enter host cells, no study has systematically assessed the ACE2 expression in the lungs of patients with these diseases. Here, we analyzed over 700 lung transcriptome samples of patients with comorbidities associated with severe COVID-19 and found that ACE2 was highly expressed in these patients, compared to control individuals. This finding suggests that patients with such comorbidities may have higher chances of developing severe COVID-19. Correlation and network analyses revealed many potential regulators of ACE2 in the human lung, including genes related to histone modifications, such as HAT1, HDAC2, and KDM5B. Our systems biology approach offers a possible explanation for increase of COVID-19 severity in patients with certain comorbidities.
format Online
Article
Text
id pubmed-7377288
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-73772882020-09-11 ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19 Pinto, Bruna G G Oliveira, Antonio E R Singh, Youvika Jimenez, Leandro Gonçalves, Andre N A Ogava, Rodrigo L T Creighton, Rachel Peron, Jean Pierre Schatzmann Nakaya, Helder I J Infect Dis Major Article Patients who died from COVID-19 often had comorbidities, such as hypertension, diabetes, and chronic obstructive lung disease. Although angiotensin-converting enzyme 2 (ACE2) is crucial for SARS-CoV2 to bind and enter host cells, no study has systematically assessed the ACE2 expression in the lungs of patients with these diseases. Here, we analyzed over 700 lung transcriptome samples of patients with comorbidities associated with severe COVID-19 and found that ACE2 was highly expressed in these patients, compared to control individuals. This finding suggests that patients with such comorbidities may have higher chances of developing severe COVID-19. Correlation and network analyses revealed many potential regulators of ACE2 in the human lung, including genes related to histone modifications, such as HAT1, HDAC2, and KDM5B. Our systems biology approach offers a possible explanation for increase of COVID-19 severity in patients with certain comorbidities. Oxford University Press 2020-06-11 /pmc/articles/PMC7377288/ /pubmed/32526012 http://dx.doi.org/10.1093/infdis/jiaa332 Text en © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Major Article
Pinto, Bruna G G
Oliveira, Antonio E R
Singh, Youvika
Jimenez, Leandro
Gonçalves, Andre N A
Ogava, Rodrigo L T
Creighton, Rachel
Peron, Jean Pierre Schatzmann
Nakaya, Helder I
ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title_full ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title_fullStr ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title_full_unstemmed ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title_short ACE2 Expression is Increased in the Lungs of Patients with Comorbidities Associated with Severe COVID-19
title_sort ace2 expression is increased in the lungs of patients with comorbidities associated with severe covid-19
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377288/
https://www.ncbi.nlm.nih.gov/pubmed/32526012
http://dx.doi.org/10.1093/infdis/jiaa332
work_keys_str_mv AT pintobrunagg ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT oliveiraantonioer ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT singhyouvika ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT jimenezleandro ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT goncalvesandrena ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT ogavarodrigolt ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT creightonrachel ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT peronjeanpierreschatzmann ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19
AT nakayahelderi ace2expressionisincreasedinthelungsofpatientswithcomorbiditiesassociatedwithseverecovid19