| Literature DB >> 24753754 |
Juan Ren1, Yuelang Zhang2, Hui Cai3, Hongbing Ma4, Dongli Zhao1, Xiaozhi Zhang1, Zongfang Li4, Shufeng Wang1, Jiangsheng Wang1, Rui Liu1, Yi Li1, Jiansheng Qian1, Hongxia Wei1, Liying Niu1, Yan Liu1, Lisha Xiao3, Muyang Ding3, Shiwen Jiang5.
Abstract
G-protein coupled receptor 4 (GPR4) belongs to a protein family comprised of 3 closely related G protein-coupled receptors. Recent studies have shown that GPR4 plays important roles in angiogenesis, proton sensing, and regulating tumor cells as an oncogenic gene. How GPR4 conducts its functions? Rare has been known. In order to detect the genes related to GPR4, microarray technology was employed. GPR4 is highly expressed in human vascular endothelial cell HMEC-1. Small interfering RNA against GPR4 was used to knockdown GPR4 expression in HMEC-1. Then RNA from the GPR4 knockdown cells and control cells were analyzed through genome microarray. Microarray results shown that among the whole genes and expressed sequence tags, 447 differentially expressed genes were identified, containing 318 up-regulated genes and 129 down-regulated genes. These genes whose expression dramatically changed may be involved in the GPR4 functions. These genes were related to cell apoptosis, cytoskeleton and signal transduction, cell proliferation, differentiation and cell-cycle regulation, gene transcription and translation and cell material and energy metabolism.Entities:
Keywords: GPR4; RNAi; microarray
Year: 2014 PMID: 24753754 PMCID: PMC3992399
Source DB: PubMed Journal: Int J Clin Exp Med ISSN: 1940-5901