| Name | PABPC5 antisense RNA 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough the presented abstracts focus extensively on lysophosphatidic acid (LPA) signaling and its receptors in processes such as fibrosis, cellular proliferation, migration, neurogenesis, and tissue remodeling, none of the studies make any mention of PABPC5‐AS1. In these reports, LPA–LPA receptor pathways are shown to contribute to aberrant wound‐healing responses leading to pulmonary and renal fibrosis, to the regulation of adipogenesis through LPA1‐mediated inhibition of PPARγ expression, and to the modulation of neurogenic and myelination processes in the central and peripheral nervous systems."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": " \n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional abstracts document the roles of LPA receptors in orchestrating cytoskeletal reorganization for cell migration, survival, and invasion in settings as diverse as cancer progression, diabetic nephropathy, and atherosclerotic plaque development. They provide detailed insights into downstream signaling mechanisms including activation of pathways such as ERK/MAPK, PI3K/AKT, and Rho–ROCK, as well as emphasize the importance of receptor‐mediated effects on neurobehavioral outcomes and vascular remodeling."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "6"}]}, {"type": "t", "text": " \n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nDespite the wealth of data on the impact of LPA signaling in both normal physiology and pathology outlined across these studies, there is no information provided regarding the function or regulation of the long non‐coding RNA PABPC5‐AS1. Thus, while these investigations elucidate multiple facets of LPA receptor biology—from mediating tissue fibrosis to influencing neurodevelopment and metabolic regulation—they do not establish any role for PABPC5‐AS1. Future studies would be required to determine if PABPC5‐AS1 interacts with, or modulates, any components of the LPA signaling cascade or whether it has distinct functions in these or other contexts."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "7", "end_ref": "9"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Andrew M Tager, Peter LaCamera, Barry S Shea, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The lysophosphatidic acid receptor LPA1 links pulmonary fibrosis to lung injury by mediating fibroblast recruitment and vascular leak."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Med (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nm1685"}], "href": "https://doi.org/10.1038/nm1685"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18066075"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18066075"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Norihiko Sakai, Jerold Chun, Jeremy S Duffield, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LPA1-induced cytoskeleton reorganization drives fibrosis through CTGF-dependent fibroblast proliferation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FASEB J (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1096/fj.12-219378"}], "href": "https://doi.org/10.1096/fj.12-219378"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23322166"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23322166"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Marie Françoise Simon, Danièle Daviaud, Jean Philippe Pradère, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Lysophosphatidic acid inhibits adipocyte differentiation via lysophosphatidic acid 1 receptor-dependent down-regulation of peroxisome proliferator-activated receptor gamma2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M412585200"}], "href": "https://doi.org/10.1074/jbc.M412585200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15710620"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15710620"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Guillermo Estivill-Torrús, Pedro Llebrez-Zayas, Elisa Matas-Rico, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Absence of LPA1 signaling results in defective cortical development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cereb Cortex (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/cercor/bhm132"}], "href": "https://doi.org/10.1093/cercor/bhm132"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17656621"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17656621"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "S M Harrison, C Reavill, G Brown, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LPA1 receptor-deficient mice have phenotypic changes observed in psychiatric disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Neurosci (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mcn.2003.09.001"}], "href": "https://doi.org/10.1016/j.mcn.2003.09.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14697676"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14697676"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Manuela Funke, Zhenwen Zhao, Yan Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The lysophosphatidic acid receptor LPA1 promotes epithelial cell apoptosis after lung injury."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Respir Cell Mol Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1165/rcmb.2010-0155OC"}], "href": "https://doi.org/10.1165/rcmb.2010-0155OC"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22021336"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22021336"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Anna Hoerder-Suabedissen, Zoltán Molnár "}, {"type": "b", "children": [{"type": "t", "text": "Molecular diversity of early-born subplate neurons."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cereb Cortex (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/cercor/bhs137"}], "href": "https://doi.org/10.1093/cercor/bhs137"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22628460"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22628460"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Elisa Matas-Rico, Beatriz García-Diaz, Pedro Llebrez-Zayas, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Deletion of lysophosphatidic acid receptor LPA1 reduces neurogenesis in the mouse dentate gyrus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Neurosci (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mcn.2008.07.014"}], "href": "https://doi.org/10.1016/j.mcn.2008.07.014"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18708146"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18708146"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Jun Xu, Yun-Ju Lai, Weei-Chin Lin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "TRIP6 enhances lysophosphatidic acid-induced cell migration by interacting with the lysophosphatidic acid 2 receptor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M311891200"}], "href": "https://doi.org/10.1074/jbc.M311891200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14688263"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14688263"}]}]}]}
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| Synonyms | CXORF46 |
| NCBI Gene ID | 102724167 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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PABPC5-AS1 has 4 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 1 datasets.
Click the + buttons to view associations for PABPC5-AS1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of PABPC5-AS1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |