| Name | long intergenic non-protein coding RNA 1415 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Although none of the three abstracts explicitly mention LINC01415 by name, the collective data from these studies suggest that long non‐coding RNAs (lncRNAs) such as LINC01415 may play important regulatory roles in cancer. In the study of esophageal squamous cell carcinoma (ESCC), an integrated analysis combining different types of RNA (including lncRNAs, mRNAs, and miRNAs) identified prognostic lncRNAs involved in complex co‐expression networks that likely modulate gene expression and signaling pathways relevant to tumor progression and clinical outcome."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Similarly, the second study used bioinformatics analyses to distinguish differentially expressed lncRNAs in ESCC and incorporated protein–protein interaction networks and survival analyses to pinpoint candidate prognostic markers; in this context, LINC01415 could represent one of the functionally significant lncRNAs that participates in carcinogenesis through regulation of coding genes and interactions within these molecular networks."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Furthermore, differences in lncRNA expression identified between lung squamous cell carcinoma and lung adenocarcinoma, including construction of competing endogenous RNA (ceRNA) networks, underscore the potential for lncRNAs like LINC01415 to modulate key pathways—such as those involving cell adhesion and PI3K‐Akt signaling—that influence tumor behavior and patient survival."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In summary, LINC01415 is implicated as a regulatory molecule that may contribute to tumor progression by participating in lncRNA–mRNA co‐expression and ceRNA networks, thereby affecting key signaling cascades and cellular processes. Its differential expression and integration within prognostic models highlight its potential utility as both a biomarker for clinical outcomes and a candidate for targeted therapeutic intervention.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Xiaobo Shi, You Li, Yuchen Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genome-wide analysis of lncRNAs, miRNAs, and mRNAs forming a prognostic scoring system in esophageal squamous cell carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PeerJ (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.7717/peerj.8368"}], "href": "https://doi.org/10.7717/peerj.8368"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32095316"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32095316"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Lu Tang, Yuqiao Chen, Xiong Peng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification and Validation of Potential Pathogenic Genes and Prognostic Markers in ESCC by Integrated Bioinformatics Analysis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Front Genet (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3389/fgene.2020.521004"}], "href": "https://doi.org/10.3389/fgene.2020.521004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33362844"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33362844"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Yingxuan Tian, Min Yu, Li Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Distinct Patterns of mRNA and lncRNA Expression Differences Between Lung Squamous Cell Carcinoma and Adenocarcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Comput Biol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/cmb.2019.0164"}], "href": "https://doi.org/10.1089/cmb.2019.0164"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31750732"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31750732"}]}]}]}
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| Synonyms | TCONS_00026208 |
| NCBI Gene ID | 100132501 |
| 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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LINC01415 has 107 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 LINC01415 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of LINC01415 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |