HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Eph receptors as cancer targets for antibody-based therapy.

Abstract
Receptor tyrosine kinases (RTKs) are integral membrane sensors that govern cell differentiation, proliferation and mobility, and enable rapid communication between cells and their environment. Of the 20 RTK subfamilies currently known, Eph receptors are the largest group. Together with their corresponding ephrin ligands, Eph receptors regulate a diverse array of physiologic processes including axonal guidance, bone remodeling, and immune cell development and trafficking. Deregulation of Eph signaling pathways is linked to cancer and other proliferative diseases and, because RTKs play critical roles in cancer development, the specific targeting of these molecules in malignancies provides a promising treatment approach. Monoclonal antibodies targeting RTKs represent a potentially attractive modality for pharmaceutical development due to their relatively high target specificity and low off-target binding rates. Therefore, new technologies to generate antibodies able to target RTKs in their native in vivo context are likely to facilitate pre-clinical and clinical development of antibody-based therapies. Our group has recently reported a platform discovery methodology termed Selection of Phage-displayed Accessible Recombinant Targeted Antibodies (SPARTA). SPARTA is a novel and robust stepwise method, which combines the attributes of in vitro screenings of a naïve human recombinant antibody library against known tumor targets with those features of in vivo selections based on tumor-homing capabilities of a pre-enriched antibody pool. This unique approach overcomes several rate-limiting challenges to generate human monoclonal antibodies amenable to rapid translation into medical applications.
AuthorsFenny H F Tang, Deodate Davis, Wadih Arap, Renata Pasqualini, Fernanda I Staquicini
JournalAdvances in cancer research (Adv Cancer Res) Vol. 147 Pg. 303-317 ( 2020) ISSN: 2162-5557 [Electronic] United States
PMID32593404 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Copyright© 2020 Elsevier Inc. All rights reserved.
Chemical References
  • Antibodies, Monoclonal
  • Antineoplastic Agents, Immunological
  • Receptors, Eph Family
Topics
  • Animals
  • Antibodies, Monoclonal (pharmacology, therapeutic use)
  • Antineoplastic Agents, Immunological (pharmacology, therapeutic use)
  • Humans
  • Molecular Targeted Therapy
  • Neoplasms (drug therapy, enzymology, pathology)
  • Receptors, Eph Family (antagonists & inhibitors, metabolism)
  • Signal Transduction

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: