| Name | long intergenic non-protein coding RNA 1963 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent investigations have highlighted the significance of long noncoding RNAs in cancer biology. In one study, lncRNA LINC01963 was shown to play a role in the progression of pancreatic carcinoma. The research focused on unveiling the molecular mechanisms by which LINC01963 contributes to tumorigenesisâpotentially by influencing cell proliferation, invasion, and other oncogenic processes that underlie pancreatic cancer development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn a related exploration of gene regulation mechanisms, another study analyzed the transcriptional control of a PKC inhibitor, PKI55. Although this work did not directly investigate LINC01963, it detailed how transcription factors such as AP1 and GAGA bind to specific promoter elements to modulate gene expression in human tissues, notably within the brain. This research underscores the broader context in which precise regulatory networks maintain cellular homeostasis and may influence disease states."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nTaken together, these studies illustrate the layered complexity of gene regulation in human diseases. On one hand, LINC01963 emerges as a potentially critical factor in pancreatic carcinoma progression, suggesting that its dysregulation could be a driver of oncogenesis. On the other, the detailed understanding of transcription factor interactions with promoter regions in the regulation of PKI55 reinforces the importance of coordinated control at both the transcriptional and postâtranscriptional levels. Such insights establish a foundation for future research aimed at therapeutically targeting these regulatory processes in cancer and other pathologies."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kailiang Li, Hongchao Han, Wenjing Gu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long non-coding RNA LINC01963 inhibits progression of pancreatic carcinoma by targeting miR-641/TMEFF2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Pharmacother (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopha.2020.110346"}], "href": "https://doi.org/10.1016/j.biopha.2020.110346"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32559621"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32559621"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Monica Borgatti, Alessia Finotti, Sofia Falzarano, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structural characterization of promoter sequences of the gene coding human PKI55 protein, a protein kinase C inhibitor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochimie (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biochi.2008.11.007"}], "href": "https://doi.org/10.1016/j.biochi.2008.11.007"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19095038"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19095038"}]}]}]}
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| NCBI Gene ID | 150967 |
| 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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LINC01963 has 446 functional associations with biological entities spanning 2 categories (chemical, cell line, cell type or tissue) extracted from 2 datasets.
Click the + buttons to view associations for LINC01963 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GTEx Tissue-Specific Aging Signatures | tissue samples with high or low expression of LINC01963 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. | |
| LINCS L1000 CMAP Chemical Perturbation Consensus Signatures | small molecule perturbations changing expression of LINC01963 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset. | |