LINC01228 Gene

Name long intergenic non-protein coding RNA 1228
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Long intergenic non‐coding RNA DYNLRB2‐2 (LINC01228) has emerged as an important regulator of cholesterol homeostasis and inflammatory responses in macrophage‐derived foam cells. In vitro studies demonstrate that exposure to oxidized LDL triggers the upregulation of LINC01228, which in turn induces the expression of G protein‐coupled receptor 119 (GPR119) and the cholesterol transporter ABCA1 via glucagon‐like peptide receptor signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Enhanced ABCA1 expression promotes apoA-I–mediated cholesterol efflux, thereby reducing intracellular cholesterol accumulation and mitigating proinflammatory cytokine release in foam cells. Further investigations indicate that modulation of LINC01228 can affect cholesterol metabolism through regulation of toll‐like receptor 2 (TLR2) expression"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ", underscoring its role in the control of lipid metabolism. In addition, LINC01228 is grouped among a broader class of long noncoding RNAs that orchestrate gene networks involved in hepatic lipid regulation and metabolic disease."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Together, these findings suggest that LINC01228 contributes to the maintenance of lipid balance and the attenuation of inflammatory pathways in atherosclerotic pathologies, making it a promising target for therapeutic intervention in cardiovascular and metabolic disorders.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yan-Wei Hu, Jun-Yao Yang, Xin Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A lincRNA-DYNLRB2-2/GPR119/GLP-1R/ABCA1-dependent signal transduction pathway is essential for the regulation of cholesterol homeostasis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Lipid Res (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1194/jlr.M044669"}], "href": "https://doi.org/10.1194/jlr.M044669"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24493833"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24493833"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yongqiang Li, Shuxin Shen, Shoukun Ding, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LincRNA DYN-LRB2-2 upregulates cholesterol efflux by decreasing TLR2 expression in macrophages."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.26352"}], "href": "https://doi.org/10.1002/jcb.26352"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28815701"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28815701"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yulan Zhao, Jianguo Wu, Suthat Liangpunsakul, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long Non-coding RNA in Liver Metabolism and Disease: Current Status."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Liver Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.livres.2017.09.001"}], "href": "https://doi.org/10.1016/j.livres.2017.09.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29576888"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29576888"}]}]}]}
Synonyms LINCRNA-DYNLRB2-2
NCBI Gene ID 104266962
API
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Predicted Functions View LINC01228's ARCHS4 Predicted Functions.
Co-expressed Genes View LINC01228's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View LINC01228's ARCHS4 Predicted Functions.

Functional Associations

LINC01228 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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If available, associations are ranked by standardized value

Dataset Summary