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http://purl.uniprot.org/citations/33267708http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33267708http://www.w3.org/2000/01/rdf-schema#comment"To explore the role and mechanism of CERS1 in hypophysoma and investigate whether CERS1 overexpression can change the autophagy process of hypophysoma, and then to explore whether CERS1's effect was regulated by the PI3K/AKT signaling pathway. Western blot and RT-PCR were used to analyze the expression or mRNA level of CERS1 at different tissues or cell lines. Afterwards, the occurrence and development of hypophysoma in vivo and in vitro, respectively, was observed by using CERS1 overexpression by lentivirus. Finally, MK-2206 and LY294002 were applied to discuss whether the role of CERS1 was regulated by the PI3K/AKT signaling pathway. Results show that the CERS1 expression and mRNA level in tumor or AtT-20 cells were decreased. CERS1 over-expressed by lentivirus could inhibit hypophysoma development in vivo and in vitro by reducing tumor volume and weight, weakening tumor proliferation and invasion, and enhancing apoptosis. In addition, shCERS1 could reverse the process. The above results indicate that CERS1 is possibly able to enhance autophagy in hypophysoma through the PI3K/AKT signaling pathway."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.org/dc/terms/identifier"doi:10.1177/1533033820977536"xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/author"Li X."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/author"Ma D."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/author"Wang J."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/author"Zhang J."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/name"Technol Cancer Res Treat"xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/pages"1533033820977536"xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/title"The Potential Role of CERS1 in Autophagy Through PI3K/AKT Signaling Pathway in Hypophysoma."xsd:string
http://purl.uniprot.org/citations/33267708http://purl.uniprot.org/core/volume"19"xsd:string
http://purl.uniprot.org/citations/33267708http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33267708
http://purl.uniprot.org/citations/33267708http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33267708
http://purl.uniprot.org/uniprot/#_B4DE47-mappedCitation-33267708http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/#_P27539-mappedCitation-33267708http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/#_P27544-mappedCitation-33267708http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/#_Q5XG75-mappedCitation-33267708http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/P27539http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/Q5XG75http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/B4DE47http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33267708
http://purl.uniprot.org/uniprot/P27544http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/33267708