Indexé dans
  • Ouvrir la porte J
  • Genamics JournalSeek
  • CiteFactor
  • Cosmos SI
  • Scimago
  • Répertoire des périodiques d'Ulrich
  • Bibliothèque des revues électroniques
  • RechercheRef
  • Université Hamdard
  • EBSCO AZ
  • Répertoire d'indexation des résumés pour les revues
  • OCLC - WorldCat
  • Invocation de Proquête
  • érudit
  • ROUTE
  • Bibliothèque virtuelle de biologie (vifabio)
  • Publions
  • Fondation genevoise pour la formation et la recherche médicales
  • Google Scholar
Partager cette page
Dépliant de journal
Flyer image

Abstrait

Advantages and Disadvantages of Targeting the C-erbB Family of Receptors in Cancer Treatment: A Review

Panagiotis Papanastasopoulos

C-erbB (EGFR) signaling is well known to promote cancer invasiveness and metastasis. Several pharmacologic approaches have been used aiming to inhibit its activity, ie monoclonal antibodies, antibody-like molecules (peptidomimetics) and receptor tyrosine kinase inhibitors. Several C-erbB signaling ‘inhibitors’, such as Trastuzumab, Cetuximab, gefitinib, erlotinib and lapatinib are now widely used in clinical practice, having revolutionized the management of certain malignancies, such as HER-2 positive breast cancer. In this review, we present an overview of the mechanism of action, pharmacokinetic properties, mechanism of resistance as well as the relative cost of administration for each group of EGFR inhibitors separately.