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http://purl.uniprot.org/citations/33045131http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33045131http://www.w3.org/2000/01/rdf-schema#comment"This study detected the expression pattern of miR-1471 in non-small-cell lung cancer (NSCLC) tissues, and analyzed the prognostic significance of miR-1471 in NSCLC. Subsequently, potential targets of miR-1471 were screened for assessing the potential molecular mechanism in NSCLC. A total of 47 primary NSCLC cases treated by radical resection and systematic lymphadenectomy in the department of thoracic surgery were collected, as well as their clinical data. MiR-1471 levels in NSCLC tissues were detected by quantitative real-time polymerase chain reaction. The prognostic potential of miR-1471 in NSCLC was assessed by Kaplan-Meier method, followed by log-rank test. Potential target genes of miR-1471 and the binding sites were predicted by bioinformatics analysis, and screened for the optimal one. The binding relationship between miR-1471 and the target FOXL1 was examined by dual-luciferase reporter assay. Subsequently, biological functions of miR-1471 and FOXL1 in NSCLC cell functions were explored by cell counting kit-8 (CCK-8), 5-ethynyl-2'-deoxyuridine (EdU) assay and flow cytometry. MiR-1471 was downregulated in NSCLC tissues and its level was correlated to TNM staging in NSCLC patients. Overall survival was poor in NSCLC patients expressing low level of miR-1471. Overexpression of miR-1471 attenuated proliferative ability and arrested cell cycle progression in G1/S phase. FOXL1 was confirmed to be the target gene binding miR-1471. Its expression pattern and biological functions in NSCLC cells were contrary to those of miR-1471. MiR-1471 is downregulated in NSCLC samples, which is related to TNM staging and prognosis in NSCLC patients. Therefore, miR-1471 suppresses the malignant aggravation of NSCLC via inhibiting the translation of FOXL1 mRNA. In addition, it could be used as an effective biomarker for predicting the prognosis in NSCLC."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.org/dc/terms/identifier"doi:10.1002/biof.1661"xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/author"Li G."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/author"Shi D."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/author"Zhao Y."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/author"Zhang K."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/name"Biofactors"xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/pages"734-742"xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/title"MiR-1471 protects the aggravation of non-small-cell lung carcinoma by targeting FOXL1."xsd:string
http://purl.uniprot.org/citations/33045131http://purl.uniprot.org/core/volume"46"xsd:string
http://purl.uniprot.org/citations/33045131http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33045131
http://purl.uniprot.org/citations/33045131http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33045131
http://purl.uniprot.org/uniprot/#_Q12952-mappedCitation-33045131http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33045131
http://purl.uniprot.org/uniprot/#_Q498Y4-mappedCitation-33045131http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33045131
http://purl.uniprot.org/uniprot/Q498Y4http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33045131
http://purl.uniprot.org/uniprot/Q12952http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33045131