| Literature DB >> 32027502 |
Maxime Liberelle1,2, Nicolas Jonckheere1,3, Patricia Melnyk1,2, Isabelle Van Seuningen1,3, Nicolas Lebègue1,2.
Abstract
Membrane-bound mucins belong to a heterogeneous family of large O-glycoproteins involved in numerous cancers and inflammatory diseases of the epithelium. Some of them are also involved in protein-protein interactions, with receptor tyrosine kinase ErbB2, and fundamental and clinical data showed that these complexes have a detrimental impact on cancer outcome, thus raising interest in therapeutic targeting. This paper aims to demonstrate that MUC3, MUC4, MUC12, MUC13, and MUC17 have a common evolutionary origin and share a common structural organization with EGF-like and SEA domains. Theoretical structure-function relationship analysis of the conserved domains indicated that the studied membrane-bound mucins share common biological properties along with potential specific functions. Finally, the potential druggability of these complexes is discussed, revealing ErbB2-related pathways of cell signaling to be targeted.Entities:
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Year: 2020 PMID: 32027502 DOI: 10.1021/acs.jmedchem.9b02001
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446