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EDG4 (show LPAR2 Proteins) and EDG7 map to q2.1 of pig chromosome 2 (SSC2 (show ELOVL2 Proteins)) and q2.6-3.2 of pig chromosome6 (SSC6), respectively
EDG7 was regulated by pregnancy stage and status. EDG7 expression was highest on d 12 pregnancy, and localized to the luminal and glandular epithelium, and EDG7 mRNA levels were elevated by estrogen in the endometrium.
myeloma cells stimulate mesenchymal stem cells (MSCs to produce autotaxin (show ENPP2 Proteins), an indispensable enzyme for the biosynthesis of lysophosphatidic acid, and LPA receptor 1 (LPA1 (show LPAR1 Proteins)) and 3 (LPA3) transduce opposite signals to MSCs to determine the fate of MSCs.
Expression profiles reveal LPAR3 (lysophosphatidic acid receptor 3) as a mediator for mitotic phosphorylation-driven pancreatic cell motility and invasion. Together, this work identifies YAP (show YAP1 Proteins) as a novel regulator of pancreatic cancer cell motility, invasion and metastasis.
These data indicated that the expression of LPA receptor 3 was increased in human triple-negative breast cancers and is associated with tumor metastatic ability.
Suggest that LPA2 (show LPAR2 Proteins) and LPA3 may function as a molecular switch and play opposing roles during megakaryopoiesis of K562 cells.
The results demonstrate LPA (show APOA Proteins)-stimulated migration in oral carcinoma cells through LPAR3, mediated further by PKC (show PRRT2 Proteins), which acts either in concert with or independently of EGFR (show EGFR Proteins) transactivation
Findings indicate lysophosphatidic acid (LPA (show APOA Proteins))-lysophosphatidic acid receptor-Galpha13 (show GNA13 Proteins) signaling node as a therapeutic target for pancreatic cancer treatment and control.
LPA3 mRNA is clearly expressed in human PANC-1 tumor cells.
Lysophosphatidic acid (LPA) increased hepatocellular carcinoma cells cell invasion, which was LPA-receptor dependent.
in the normal human menstrual cycle, lysophosphatidic acid receptor 3 messenger RNA and protein expression change, indicating that this gene may be related to the function of the endometrium.
The results indicated that LPA(3) acts as a positive regulator of cell motility and invasion in sarcoma cells, suggesting that LPA (show APOA Proteins) signaling pathway via LPA(3) may be involved in the progression of sarcoma cells.
These results indicate that ATX (show ENPP2 Proteins)-lysophosphatidic acid-LPA3 signaling at the embryo-epithelial boundary induces decidualization via the canonical HB-EGF (show HBEGF Proteins) and COX-2 pathways.
Lpar3(-/-) female mice had delayed embryo implantation.
These results suggest that LPA3 receptor-mediated amplification of spinal LPA production is required for the development of paclitaxel-induced neuropathic pain.
These results suggest that LPA signaling through LPA3 may inhibit angiogenesis and fibroblast activation in mouse lung cancer cells
The thromboxane A(2) receptor agonist 11-deoxy PGF (show PTGFR Proteins)(2alpha) can partially alleviate embryo crowding in the Lpar3((-/-)) females and embryo crowding likely contributes to reduced litter size in the Lpar3((-/-)) females.
Lysophosphatidic acid, via LPA(1 (show LPAR1 Proteins)) and LPA(3) receptors, may play a significant role in inducing and/or sustaining the massive infiltration of leukocytes during inflammation
Luminal epithelium localization and up-regulation by progesterone differentiate LPA3 from the other nine LP receptors and may underlie its essential role in embryo implantation.
LPA(1 (show LPAR1 Proteins)-3) are differentially expressed in the central nervous system and their expression is upregulated in response to injury.
Lysophosphatidic acid receptors LPA3 and LPA1 (show LPAR1 Proteins) promote CXCL12 (show CXCL12 Proteins)-mediated smooth muscle progenitor cell recruitment.
LPA3 receptor-mediated signalling has an influence on embryo implantation, and there is a linkage between LPA signalling and prostaglandin biosynthesis.
This gene encodes a member of the G protein-coupled receptor family, as well as the EDG family of proteins. This protein functions as a cellular receptor for lysophosphatidic acid and mediates lysophosphatidic acid-evoked calcium mobilization. This receptor couples predominantly to G(q/11) alpha proteins.
endothelial differentiation, lysophosphatidic acid G-protein-coupled receptor, 7
, lysophosphatidic acid receptor 3
, LPA receptor 3
, LPA receptor EDG7
, calcium-mobilizing lysophosphatidic acid receptor LP-A3
, endothelial cell differentiation gene 7
, lysophosphatidic acid receptor Edg-7
, endothelial differentiation, lysophosphatidic acid G-protein-coupled receptor 7
, putative G protein-coupled receptor snGPCR32