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A genome-wide association study of survival in small-cell lung cancer patients treated with irinotecan plus cisplatin chemotherapy.
Han, J-Y; Lee, Y-S; Shin, E Soon; Hwang, J-A; Nam, S; Hong, S-H; Ghang, H Young; Kim, J Young; Yoon, S Jin; Lee, J Soo.
Afiliação
  • Han JY; Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Lee YS; Functional Genomic Branch, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Shin ES; DNALink, Seoul, Republic of Korea.
  • Hwang JA; Functional Genomic Branch, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Nam S; Functional Genomic Branch, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Hong SH; Functional Genomic Branch, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Ghang HY; Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.
  • Kim JY; Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Yoon SJ; Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
  • Lee JS; Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Pharmacogenomics J ; 14(1): 20-7, 2014 Feb.
Article em En | MEDLINE | ID: mdl-23478653
ABSTRACT
We conducted a genome-wide association study (GWAS) to identify single nucleotide polymorphisms (SNPs) influencing overall survival (OS) of small-cell lung cancer (SCLC) patients. We prospectively collected blood samples from 139 SCLC patients who participated in phase II studies of irinotecan and cisplatin (IP) chemotherapy as first-line therapy. Among 334 127 SNPs, which passed quality control, seven showed significant association with OS. The rs16950650CT, rs7186128AG or GG, rs17574269AG, rs8020368CC, rs4655567CC, rs2166219TT or rs2018683TT showed shorter OS compared with control alleles. Among the seven SNPs, rs4655567, rs8020368 and rs2018683 were significantly associated with a resistant relapse (RR). In the multivariate analysis, rs8020368CC was significantly associated with higher risk of RR (odds ratio=16.7, P=0.007). In vitro and in silico analysis showed that SNPs in C14orf49 might be associated with epithelial-to-mesenchymal transition. This exploratory GWAS identified candidate SNPs that may be predictive of the clinical outcome of SCLC patients receiving IP.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Polimorfismo de Nucleotídeo Único / Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pharmacogenomics J Assunto da revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Polimorfismo de Nucleotídeo Único / Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pharmacogenomics J Assunto da revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Ano de publicação: 2014 Tipo de documento: Article