Protein Lipidation by Palmitoylation and Myristoylation in Cancer

被引：45

作者：

Fhu, Chee Wai ^{[1
]}

Ali, Azhar ^{[1
]}

机构：

[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore

来源：

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 9卷

关键词：

protein lipidation; palmitoylation; myristoylation; depalmitoylation; metabolism; cancer; TRIS DIBENZYLIDENEACETONE DIPALLADIUM; N-MYRISTOYLTRANSFERASE; MEMBRANE-BINDING; DYNAMIC PALMITOYLATION; POTENT INHIBITORS; S-PALMITOYLATION; THIOESTERASES; DBA PALLADIUM; PALMOSTATIN B; FATTY-ACIDS;

D O I：

10.3389/fcell.2021.673647

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Posttranslational modification of proteins with lipid moieties is known as protein lipidation. The attachment of a lipid molecule to proteins endows distinct properties, which affect their hydrophobicity, structural stability, localization, trafficking between membrane compartments, and influences its interaction with effectors. Lipids or lipid metabolites can serve as substrates for lipidation, and the availability of these lipid substrates are tightly regulated by cellular metabolism. Palmitoylation and myristoylation represent the two most common protein lipid modifications, and dysregulation of protein lipidation is strongly linked to various diseases such as metabolic syndromes and cancers. In this review, we present recent developments in our understanding on the roles of palmitoylation and myristoylation, and their significance in modulating cancer metabolism toward cancer initiation and progression.

引用

页数：15

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