A narrative review of the role of Eph receptors in head and neck squamous cell carcinoma

Publikation: Beitrag in FachzeitschriftÜbersichtsartikel (Review)BeigetragenBegutachtung

Beitragende

  • Aisha A H Al-Jamaei - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Ramadugula V Subramanyam - , K M Shah Dental College and Hospital (Autor:in)
  • Marco N Helder - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Tymour Forouzanfar - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Erik H van der Meij - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Sayida Al-Jamei - , OncoRay - Nationales Zentrum für Strahlenforschung in der Onkologie, Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Jan G A M de Visscher - , Amsterdam University Medical Centers (UMC) (Autor:in)

Abstract

Tyrosine kinase receptors (TKR) coordinate a variety of pathological processes in head and neck squamous cell carcinoma (HNSCC), and eventually play a role in patient outcomes. In this review, the role of Eph receptors in HNSCC progression and the possibility of targeting these receptors are illustrated. All relevant studies were identified through a comprehensive search of four electronic databases, including PubMed, Scopus, web of science, and Embase till August 2022. EphA2 and EphB4, along with ephrin-B2, were the most extensively studied proteins in this family. However, overexpression of EphB4 and its ligand ephrin-B2 were the only proteins that consistently showed association with a poor outcome, indicating that these proteins might serve as valuable prognostic markers in HNSCC. High expression of EphA3 and EphB4 was found to play a crucial role in radioresistance of HNSCC. EphB4 loss, in particular, was observed to induce an immunosuppression phenotypic HNSCC. Currently, ongoing clinical trials are investigating the benefits of EphB4-ephrin-B2 blockade in combination with standard of care treatment in HNSCC. Further efforts are needed to explore the biological role and behavioral complexity of this family of TKR in HNSCC with great attention to avoid heterogeneity of HNSCC subsites.

Details

OriginalspracheEnglisch
Seiten (von - bis)833-845
Seitenumfang13
FachzeitschriftOral diseases
Jahrgang30
Ausgabenummer3
Frühes Online-Datum6 Juni 2023
PublikationsstatusVeröffentlicht - Apr. 2024
Peer-Review-StatusJa

Externe IDs

Scopus 85161612324
Mendeley a8565ae1-9494-350e-93b1-bced4a352745

Schlagworte

Bibliotheksschlagworte