Recent advances of the Ephrin and Eph family in cardiovascular development and pathologies.

Cardiovascular medicine Cell biology

Journal

iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038

Informations de publication

Date de publication:
16 Aug 2024
Historique:
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: epublish

Résumé

Erythropoietin-producing hepatoma (Eph) receptors, comprising the largest family of receptor tyrosine kinases (RTKs), exert profound influence on diverse biological processes and pathological conditions such as cancer. Interacting with their corresponding ligands, erythropoietin-producing hepatoma receptor interacting proteins (Ephrins), Eph receptors regulate crucial events like embryonic development, tissue boundary formation, and tumor cell survival. In addition to their well-established roles in embryonic development and cancers, emerging evidence highlights the pivotal contribution of the Ephrin/Eph family to cardiovascular physiology and pathology. Studies have elucidated their involvement in cardiovascular development, atherosclerosis, postnatal angiogenesis, and, more recently, cardiac fibrosis and calcification, suggesting a promising avenue for therapeutic interventions in cardiovascular diseases. There remains a need for a comprehensive synthesis of their collective impact in the cardiovascular context. By exploring the intricate interactions between Eph receptors, ephrins, and cardiovascular system, this review aims to provide a holistic understanding of their roles and therapeutic potential in cardiovascular health and diseases.

Identifiants

pubmed: 39188984
doi: 10.1016/j.isci.2024.110556
pii: S2589-0042(24)01781-4
pmc: PMC11345580
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

110556

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare no competing interests.

Auteurs

Yuan Zhu (Y)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Sheng-An Su (SA)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Jian Shen (J)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Hong Ma (H)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Jixie Le (J)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Yao Xie (Y)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Meixiang Xiang (M)

Department of Cardiology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
State Key Laboratory of Transvascular Implantation Devices, Hangzhou 310009, China.

Classifications MeSH