The Glycobiology of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a progressive pulmonary vascular disease of complex etiology. Cases of PAH that do not receive therapy after diagnosis have a low survival rate. Multiple reports have shown that idiopathic PAH, or IPAH, is associated with metabolic dysregulation including alt...

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Main Authors: Shia Vang, Phillip Cochran, Julio Sebastian Domingo, Stefanie Krick, Jarrod Wesley Barnes
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Metabolites
Subjects:
Online Access:https://www.mdpi.com/2218-1989/12/4/316
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author Shia Vang
Phillip Cochran
Julio Sebastian Domingo
Stefanie Krick
Jarrod Wesley Barnes
author_facet Shia Vang
Phillip Cochran
Julio Sebastian Domingo
Stefanie Krick
Jarrod Wesley Barnes
author_sort Shia Vang
collection DOAJ
description Pulmonary arterial hypertension (PAH) is a progressive pulmonary vascular disease of complex etiology. Cases of PAH that do not receive therapy after diagnosis have a low survival rate. Multiple reports have shown that idiopathic PAH, or IPAH, is associated with metabolic dysregulation including altered bioavailability of nitric oxide (NO) and dysregulated glucose metabolism. Multiple processes such as increased proliferation of pulmonary vascular cells, angiogenesis, apoptotic resistance, and vasoconstriction may be regulated by the metabolic changes demonstrated in PAH. Recent reports have underscored similarities between metabolic abnormalities in cancer and IPAH. In particular, increased glucose uptake and altered glucose utilization have been documented and have been linked to the aforementioned processes. We were the first to report a link between altered glucose metabolism and changes in glycosylation. Subsequent reports have highlighted similar findings, including a potential role for altered metabolism and aberrant glycosylation in IPAH pathogenesis. This review will detail research findings that demonstrate metabolic dysregulation in PAH with an emphasis on glycobiology. Furthermore, this report will illustrate the similarities in the pathobiology of PAH and cancer and highlight the novel findings that researchers have explored in the field.
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spelling doaj.art-0bdbc6f25d4145be99f2a85a8950aaba2023-12-03T13:42:55ZengMDPI AGMetabolites2218-19892022-04-0112431610.3390/metabo12040316The Glycobiology of Pulmonary Arterial HypertensionShia Vang0Phillip Cochran1Julio Sebastian Domingo2Stefanie Krick3Jarrod Wesley Barnes4Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USADivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USADivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USADivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USADivision of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USAPulmonary arterial hypertension (PAH) is a progressive pulmonary vascular disease of complex etiology. Cases of PAH that do not receive therapy after diagnosis have a low survival rate. Multiple reports have shown that idiopathic PAH, or IPAH, is associated with metabolic dysregulation including altered bioavailability of nitric oxide (NO) and dysregulated glucose metabolism. Multiple processes such as increased proliferation of pulmonary vascular cells, angiogenesis, apoptotic resistance, and vasoconstriction may be regulated by the metabolic changes demonstrated in PAH. Recent reports have underscored similarities between metabolic abnormalities in cancer and IPAH. In particular, increased glucose uptake and altered glucose utilization have been documented and have been linked to the aforementioned processes. We were the first to report a link between altered glucose metabolism and changes in glycosylation. Subsequent reports have highlighted similar findings, including a potential role for altered metabolism and aberrant glycosylation in IPAH pathogenesis. This review will detail research findings that demonstrate metabolic dysregulation in PAH with an emphasis on glycobiology. Furthermore, this report will illustrate the similarities in the pathobiology of PAH and cancer and highlight the novel findings that researchers have explored in the field.https://www.mdpi.com/2218-1989/12/4/316pulmonary hypertensionglycobiologymetabolism
spellingShingle Shia Vang
Phillip Cochran
Julio Sebastian Domingo
Stefanie Krick
Jarrod Wesley Barnes
The Glycobiology of Pulmonary Arterial Hypertension
Metabolites
pulmonary hypertension
glycobiology
metabolism
title The Glycobiology of Pulmonary Arterial Hypertension
title_full The Glycobiology of Pulmonary Arterial Hypertension
title_fullStr The Glycobiology of Pulmonary Arterial Hypertension
title_full_unstemmed The Glycobiology of Pulmonary Arterial Hypertension
title_short The Glycobiology of Pulmonary Arterial Hypertension
title_sort glycobiology of pulmonary arterial hypertension
topic pulmonary hypertension
glycobiology
metabolism
url https://www.mdpi.com/2218-1989/12/4/316
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