粘蛋白
可药性
化学
糖蛋白
受体酪氨酸激酶
信号转导
酪氨酸激酶
细胞生物学
受体
生物化学
计算生物学
生物
基因
作者
Maxime Liberelle,Nicolas Jonckheere,Patricia Melnyk,Isabelle Van Seuningen,Nicolas Lebègue
标识
DOI:10.1021/acs.jmedchem.9b02001
摘要
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.
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