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http://purl.uniprot.org/citations/30287284http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30287284http://www.w3.org/2000/01/rdf-schema#comment"Integrin-interacting protein Kindlin-2, as a focal adhesion protein, promotes growth and progression of breast cancer. However, the precise mechanism that underlie the role of Kindlin-2 in breast cancer is elusive. Here, we report that the expression of Kindlin-2 positively correlated with DNA methyltransferase 1(DNMT1) in breast cancer patients. Further, we found that DNMT1 was upregulated in mammary gland tissues of mammary specific Kindlin-2 transgenic mice. More importantly, high expression of DNMT1 was observed in mammary tumors formed by Kindlin-2 transgenic mice. On the basis of these observations, DNMT inhibitor 5-aza-CdR was used and found its treatment strongly decreased Kindlin-2-induced breast cancer cell proliferation and migration. Mechanistically, Kindlin-2 increased the stability of DNA methyltransferase DNMT1 through interaction with DNMT1 and methylated CpG islands in the E-cadherin promoter. Kindlin-2 increased the occupancy of DNMT1 at E-cadherin promoter, thereby suppressing E-cadherin expression. Taken together, our data reveal that Kindlin-2 promotes breast cancer development by enhancing the stability of DNMT1."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.org/dc/terms/identifier"doi:10.1016/j.biocel.2018.09.022"xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Li B."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Qi L."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Wu J."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Zhang X."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Zhang H."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Yu Y."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Wang P."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/author"Chu W."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/name"Int J Biochem Cell Biol"xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/pages"41-51"xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/title"Kindlin-2 interacts with and stabilizes DNMT1 to promote breast cancer development."xsd:string
http://purl.uniprot.org/citations/30287284http://purl.uniprot.org/core/volume"105"xsd:string
http://purl.uniprot.org/citations/30287284http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30287284
http://purl.uniprot.org/citations/30287284http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30287284
http://purl.uniprot.org/uniprot/#_A8K6S3-mappedCitation-30287284http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30287284
http://purl.uniprot.org/uniprot/#_Q96AC1-mappedCitation-30287284http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30287284
http://purl.uniprot.org/uniprot/A8K6S3http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30287284
http://purl.uniprot.org/uniprot/Q96AC1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30287284