http://purl.uniprot.org/citations/25927928 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/25927928 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundThe emergence of drug resistance in cancer patients limits the success rate of clinical chemotherapy. MicroRNAs (miRNAs) may play a role in chemoresistance and may be involved in modulating of some drug resistance-related pathways in cancer cells. In this study, the involvement of microRNA-148b (miR-148b) and its roles in the development of chemoresistance in lung cancer are determined.MethodsThis study was performed in two lung cancer cell lines (A549 and SPC-A1). The levels of miR-148b and DNMT1 mRNA expression were determined by using Quantitative Real-Time PCR. Proteins of DNMTs are represented by western blot assay. Cell viability was assessed by MTT assay. Cell apoptosis was evaluated using flow cytometry.ResultsThe data showed a down-regulated of miR-148b expression and evaluated methyltransferases (DNMTs) expression in cisplatin-resisted human non-small cell lung cancer (NSCLC) cell line-A549/DDP and SPC-A1/DDP compared with their parental A549 and SPC-A1 cell line. In transfection experiments, miR-148b mimics reduced the DNMT1 expression, as well as enhanced the sensitivity of cells to cisplatin and cisplatin-induced apoptosis in A549/DDP or SPC-A1/DDP cells. While miR-148b inhibitor increased DNMT1 expression, as well as attenuated the sensitivity of cells to cisplatin in A549 and SPC-A1 cells. miR-148b was showed to exert negative effect on DNMT1 expression by targeting its 3'UTR in A549/DDP and A549 cells. Importantly, silenced DNMT1 increases cisplatin sensitivity of A549/DDP cells and over-expressed DNMT1 reverses pro-apoptosis effect of miR-148b mimic.ConclusionsmiR-148b reverses cisplatin-resistance in non-small cell cancer cells via negatively regulating DNMT1 expression."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.org/dc/terms/identifier | "doi:10.1186/s12967-015-0488-y"xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/author | "Jiang Y."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/author | "Li Y."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/author | "Meng F."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/author | "Sui C."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/date | "2015"xsd:gYear |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/name | "J Transl Med"xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/pages | "132"xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/title | "miR-148b reverses cisplatin-resistance in non-small cell cancer cells via negatively regulating DNA (cytosine-5)-methyltransferase 1(DNMT1) expression."xsd:string |
http://purl.uniprot.org/citations/25927928 | http://purl.uniprot.org/core/volume | "13"xsd:string |
http://purl.uniprot.org/citations/25927928 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/25927928 |
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