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http://purl.uniprot.org/citations/35130633http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/35130633http://www.w3.org/2000/01/rdf-schema#comment"Centromere protein M (CENPM) is essential for chromosome separation during mitosis. However, its roles in lung adenocarcinoma (LUAD) progression and metastasis remain unknown. In this study, we aimed to explore the effects of CENPM on LUAD progression as well as the underlying mechanisms. We analyzed the expression of CENPM and its correlation with clinicopathological characteristics using GEO LUAD chip datasets and TCGA dataset. We further investigated the impact of CENPM on LUAD and . In silico analysis and qRT-PCR revealed that CENPM is upregulated in LUAD compared with that in normal lung tissues. Via gain/loss-of-function assays, we further found that CENPM promotes the LUAD cell cycle, cell proliferation, migration and invasion, and inhibits cell apoptosis. The study showed that loss of CENPM inhibits the growth of A549 xenografts. Furthermore, we found that CENPM can promote the phosphorylation of mTOR rather than directly affect the mTOR content. Inhibition of mTOR activity abrogates the promoting effects of CENPM on cell cycle progression, cell proliferation, migration and invasion. Taken together, these results show that CENPM plays an important role in the growth and metastasis of LUAD and may be a promising therapeutic target in LUAD."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.org/dc/terms/identifier"doi:10.3724/abbs.2021013"xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Deng Z."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Liu C."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Li G."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Liu P."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Wang S."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Yang Z."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Zhou Y."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Lv L."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Hou F."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Lv J."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/author"Dao Y."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/name"Acta Biochim Biophys Sin (Shanghai)"xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/pages"99-112"xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/title"Upregulation of CENPM facilitates lung adenocarcinoma progression via PI3K/AKT/mTOR signaling pathway."xsd:string
http://purl.uniprot.org/citations/35130633http://purl.uniprot.org/core/volume"54"xsd:string
http://purl.uniprot.org/citations/35130633http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/35130633
http://purl.uniprot.org/citations/35130633http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/35130633
http://purl.uniprot.org/uniprot/#_B1AHQ6-mappedCitation-35130633http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35130633
http://purl.uniprot.org/uniprot/#_B1AHQ7-mappedCitation-35130633http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35130633
http://purl.uniprot.org/uniprot/#_B1AHQ8-mappedCitation-35130633http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35130633