Pulmonary artery smooth muscle cell phenotypic switching: A key event in the early stage of pulmonary artery hypertension

Drug Discov Today. 2023 May;28(5):103559. doi: 10.1016/j.drudis.2023.103559. Epub 2023 Mar 22.

Abstract

Pulmonary arterial hypertension (PAH) is a currently incurable pulmonary vascular disease. Since current research on PAH is mainly aimed at the middle and late stages of disease progression, no satisfactory results have been achieved. This has led researchers to focus on the early stages of PAH. This review highlights for the first time a key event in the early stages of PAH progression, namely, the occurrence of pulmonary arterial smooth muscle cell (PASMC) phenotypic switching. Summarizing the related reports of phenotypic switching provides new perspectives and directions for the early pathological progression and treatment strategies for PAH.

Keywords: early stage; phenotypic switching; pulmonary arterial hypertension; pulmonary smooth muscle cells; signaling pathways; small molecular regulators.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation / physiology
  • Humans
  • Hypertension, Pulmonary* / drug therapy
  • Myocytes, Smooth Muscle / pathology
  • Pulmonary Arterial Hypertension* / pathology
  • Pulmonary Artery / pathology
  • Signal Transduction / physiology