G-Protein-Coupled Lysophosphatidic Acid Receptors and Their Regulation of AKT Signaling

被引:53
|
作者
Riaz, Anjum [1 ]
Huang, Ying [2 ]
Johansson, Staffan [2 ]
机构
[1] Univ Punjab, Inst Biochem & Biotechnol, Lahore 54590, Pakistan
[2] Uppsala Univ, Dept Med Biochem & Microbiol, Biomed Ctr, S-75123 Uppsala, Sweden
关键词
G-protein coupled receptors (GPCR); lysophosphatidic acid (LPA); PI3K; AKT; LPA RECEPTORS; EDG FAMILY; CELL-MIGRATION; BIOACTIVE LYSOPHOSPHOLIPIDS; BIOLOGICAL ROLES; CANCER CELLS; AUTOTAXIN; ACTIVATION; EXPRESSION; IDENTIFICATION;
D O I
10.3390/ijms17020215
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A hallmark of G-protein-coupled receptors (GPCRs) is their ability to recognize and respond to chemically diverse ligands. Lysophospholipids constitute a relatively recent addition to these ligands and carry out their biological functions by activating G-proteins coupled to a large family of cell-surface receptors. This review aims to highlight salient features of cell signaling by one class of these receptors, known as lysophosphatidic acid (LPA) receptors, in the context of phosphatidylinositol 3-kinase (PI3K)-AKT pathway activation. LPA moieties efficiently activate AKT phosphorylation and activation in a multitude of cell types. The interplay between LPA, its receptors, the associated Gi/o subunits, PI3K and AKT contributes to the regulation of cell survival, migration, proliferation and confers chemotherapy-resistance in certain cancers. However, detailed information on the regulation of PI3K-AKT signals induced by LPA receptors is missing from the literature. Here, some urgent issues for investigation are highlighted.
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收藏
页数:13
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