Ontology highlight
ABSTRACT: Background
Restenosis poses a significant challenge for individuals afflicted with peripheral artery diseases, often leading to considerable morbidity and necessitating repeated interventions. The primary culprit behind the pathogenesis of restenosis is intimal hyperplasia (IH), in which the hyperproliferative and migratory vascular smooth muscle cell (VSMC) accumulate excessively in the tunica intima. 6-Phosphogluconate dehydrogenase (6PGD), sometimes referred to as PGD, is one of the critical enzymes in pentose phosphate pathway (PPP). In this study, we sought to probe whether 6PGD is aberrantly regulated in IH and contributes to VSMC phenotypic switching.Methods
We used clinical specimens of diseased human coronary arteries with IH lesions and observed robust upregulatio
SUBMITTER: Lu AL
PROVIDER: S-EPMC11420449 | biostudies-literature | 2024
REPOSITORIES: biostudies-literature