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1000 Titel
  • The Regulatory Network and Potential Role of LINC00973-miRNA-mRNA ceRNA in the Progression of Non-Small-Cell Lung Cancer
1000 Autor/in
  1. Guo, Qiang |
  2. Li, Dan |
  3. Luo, Xiangyu |
  4. Yuan, Ye |
  5. Li, Tian |
  6. Liu, Huasong |
  7. Wang, Xinju |
1000 Verlag
  • Frontiers Media S.A.
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-29
1000 Erschienen in
1000 Quellenangabe
  • 12:684807
1000 Copyrightjahr
  • 2021
1000 Embargo
  • 2022-01-31
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fimmu.2021.684807 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358408/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Abstract/Summary
  • <jats:sec><jats:title>Background</jats:title><jats:p>The occurrence and development of cancer could be promoted by abnormally competing endogenous RNAs (ceRNA) network. This article aims to determine the prognostic biomarker of ceRNA for non-small-cell lung cancer (NSCLC) prognosis.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The expression and clinical significance of LINC00973 in NSCLC tissues were analyzed <jats:italic>via</jats:italic> the The Cancer Genome Atlas (TCGA), Gene Expression Profiling Interactive Analysis (GEPIA), lnCAR, and clinical samples in Taihe Hospital. The biological functions and signaling pathways involved in target genes of ceRNA network were analyzed <jats:italic>via</jats:italic> Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). Survival analysis, univariate and multivariate Cox regression analysis were used for prognostic-related mRNA.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Expression of LINC00973 was increased in NSCLC tissues. High expression of LINC00973 was associated with poor prognosis of NSCLC patients. There were 15 miRNA and 238 differential mRNA in the INC00973-miRNA-mRNA ceRNA network, involving cell migration, endothelial cell proliferation, tumor growth factor (TGF)-β, cellular senescence, phosphatidylinositol 3-hydroxy kinase (PI3K)-Akt, Hippo, Rap1, mitogen-activated protein kinase (MAPK), cell cycle signaling pathway, etc. The expression levels of RTKN2, NFIX, PTX3, BMP2 and LOXL2 were independent risk factors for the poor prognosis of NSCLC patients.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>LINC00973-miRNA-mRNA ceRNA network might be the basis for determining pivotal post-translational regulatory mechanisms in the progression of NSCLC. BMP2, LOXL2, NFIX, PTX3 and RTKN2 might be valuable prognostic markers and potential therapeutic targets.</jats:p></jats:sec>
1000 Sacherschließung
lokal Gene Expression Regulation, Neoplastic [MeSH]
lokal Carcinoma, Non-Small-Cell Lung/genetics [MeSH]
lokal Lung Neoplasms/genetics [MeSH]
lokal ceRNA
lokal prognosis
lokal RNA, Long Noncoding/genetics [MeSH]
lokal RNA, Messenger/genetics [MeSH]
lokal LINC00973
lokal Gene Ontology [MeSH]
lokal NFI Transcription Factors/genetics [MeSH]
lokal MicroRNAs/genetics [MeSH]
lokal Carcinoma, Non-Small-Cell Lung/pathology [MeSH]
lokal Immunology
lokal Amino Acid Oxidoreductases/genetics [MeSH]
lokal Bone Morphogenetic Protein 2/genetics [MeSH]
lokal biomarker
lokal Humans [MeSH]
lokal C-Reactive Protein/genetics [MeSH]
lokal Survival Analysis [MeSH]
lokal Serum Amyloid P-Component/genetics [MeSH]
lokal Intracellular Signaling Peptides and Proteins/genetics [MeSH]
lokal Gene Regulatory Networks [MeSH]
lokal Biomarkers, Tumor/genetics [MeSH]
lokal Lung Neoplasms/pathology [MeSH]
lokal non-small cell lung cancer
lokal Signal Transduction [MeSH]
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