http://purl.uniprot.org/citations/20351547 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/20351547 | http://www.w3.org/2000/01/rdf-schema#comment | "Background and objectiveDNA repair capacity is correlated with sensitivity of cancer cells toward platinum-based chemotherapy. The aim of this study was to investigate whether single nucleotide polymorphisms (SNPs) in polymorphisms of DNA repair gene ERCC1 (excision repair cross-complementation group 1) and XPD (ERCC2, excision repair cross-complementation group 2) were associated with the tumor response in advanced non-small-cell lung cancer (NSCLC) patients received platinum-based chemotherapy in Chinese population.MethodsTotally 115 patients with advanced NSCLC were routinely treated with cisplatin- or carboplatin-based chemotherapy, and clinical response was evaluated after 2 cycles. Three dimensions (3-D) polyacrylamide gel-based DNA microarray method was used to evaluate the genotypes of ERCC1 Asn118Asn (354 CT), Gln504Lys (8092 CA) and XPD Lys751Gln (35931 AC).ResultsThe C→T change of ERCC1 Asn118Asn polymorphism and the C→A change of ERCC1 Gln504Lys polymorphism have statistically significant association with elevated or descendent platinum-based chemotherapy response respectively.ConclusionThe polymorphic status of ERCC1 might be the promising ancillary marker for predicting treatment response of advanced stage NSCLC patients. The DNA microarray-based method is accurate, high-throughput and inexpensive, suitable for SNP genotyping in a large number of individuals."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.org/dc/terms/identifier | "doi:10.1097/coc.0b013e3181b9cedc"xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Cheng H."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Chen B."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Cheng L."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Ji J."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Li F."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Lu Z."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Sun X."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Qin S."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Zhou Y."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Feng J."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/author | "Sun N."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/date | "2010"xsd:gYear |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/name | "Am J Clin Oncol"xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/pages | "489-494"xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/title | "Association between polymorphisms of ERCC1 and XPD and clinical response to platinum-based chemotherapy in advanced non-small cell lung cancer."xsd:string |
http://purl.uniprot.org/citations/20351547 | http://purl.uniprot.org/core/volume | "33"xsd:string |
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