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Over 100 years have passed since the first observation of the notched wing phenotype in Drosophila melanogaster, and significant progress has been made to characterize the role of the Notch receptor, its ligands, downstream targets, and cross-talk with other signaling pathways. The canonical Notch pathway with four Notch receptors (Notch1-4) and five ligands (DLL1, 3-4, Jagged 1-2) is an evolutionarily conserved cell signaling pathway that plays critical roles in cell-fate determination, differentiation, development, tissue patterning, cell proliferation, and death. In cancer, these roles have a critical impact on tumor behavior and response to therapy. Because the role of Notch remains tissue and context dependent, alterations within this pathway may lead to tumor suppressive or oncogenic phenotypes. Although no FDA-approved therapies currently exist for the Notch pathway, multiple therapeutics (e.g., demcizumab, tarextumab, GSI MK-0752, R04929097, and PF63084014) have been developed to target different aspects of this pathway for both hematologic and solid malignancies. Understanding the context-specific effects of the Notch pathway will be important for individualized therapies targeting this pathway.

Original publication

DOI

10.1158/1078-0432.CCR-14-0809

Type

Journal article

Journal

Clin Cancer Res

Publication Date

01/03/2015

Volume

21

Pages

955 - 961

Keywords

Animals, Antineoplastic Agents, Antineoplastic Combined Chemotherapy Protocols, Drug Discovery, Humans, Molecular Targeted Therapy, Neoplasms, Oncogene Proteins, Patient Selection, Receptors, Notch, Signal Transduction, Translational Medical Research, Tumor Suppressor Proteins