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SIRT1 基因多态性与肺癌化疗敏感性的关系
引用本文:符一岚,王瑛,尹继业,等. SIRT1 基因多态性与肺癌化疗敏感性的关系[J]. 肿瘤药学, 2013, 0(6): 426-431
作者姓名:符一岚  王瑛  尹继业  
作者单位:[1]中南大学药学院,湖南长沙410013 [2]中南大学临床药理研究所,遗传药理学湖南省重点实验室,湖南长沙410078 [3]中南大学湘雅医学院附属肿瘤医院,湖南长沙410013
基金项目:国家高技术发展计划重大专项(863项目)(NO:2012AA02A517),国家自然科学基金项目(NO:81173129,81373490).
摘    要:目的探讨S1RTl基因多态性与肺癌对以铂类为基础的化疗敏感性的关系。方法选取338名肺癌患者(其中184名对化疗耐药和154名对化疗敏感)为研究对象,所有患者均接受以铂类(顺铂、卡铂)为基础的化疗。分析其SIRTl的所有单核苷酸多态性,最后筛选出4个tagSNPs进行基因分型。OR和CI用来评估SIRTl基因多态性与肺癌患者化疗效果的相关性。结果在〉60岁的肺癌患者中,rs3758391的基因多态性与铂类化疗疗效显著相关(OR=0.38,P=0.049)。rs3740051、rsl2778366的遗传多态性与铂类化疗疗效之间无显著相关性。结论SIRTlrs3758391基因多态性可以显著影响肺癌患者铂类化疗的敏感性,SIRTl可能作为肺癌铂类化疗疗效评估的标志物。

关 键 词:S1RTl  单核苷酸多态性  肺癌  化疗敏感性

Effect of SIRT1 Genes Polymorphisms on the Chemosensitivity of Patients with Lung Cancer
Fu Yilan,Wang Ying,Yin Jiye,et al.. Effect of SIRT1 Genes Polymorphisms on the Chemosensitivity of Patients with Lung Cancer[J]. Anti-Tumor Pharmacy, 2013, 0(6): 426-431
Authors:Fu Yilan  Wang Ying  Yin Jiye  et al.
Affiliation:2" (School of Pharmaceutical Sciences, Central South University, Changsha, Hunan, 410013, China; 21nstitute of Clini- cal Pharmacology, Hunan Key Laboratory of Pharmncogencties, Central South University, Changsha, Hunan, 410078, China; 3Tumor Hospital Xiangya School of Medicine of Central South University, Changsha, Hunan, 410013, China)
Abstract:Objective To explore the relationship between the SIRT1 genetic polymorphisms and chemosensitivity to plati- num-based chemotherapy in lung cancer patients. Methods A total of 338 lung cancer patients (184 resistant and 154 sensitive) were selected and treated by platinum-based chemotherapy in this study. All single nucleotide polymorphisms in SIRT1 gene were analyzed and four tagging SNPs were finally screened for genotyped. The odds ratios (OIL) with 95 % confidence intervals (CI) were used to assess the effect of S1RT1 Genes Polymorphisms on the chemosensitivity of patients with lung cancer. Results We found a significant association of SIRT1 rs3758391 polymorphism with platinum-based chemotherapy effectiveness in lung cancer patients who were older than 60 years (OR=0.38, P = 0.049). While no significant correlation was discovered between rs3740051, rs12778366 genetic polymorphism and platinum-based chemotherapy effect . Conclusion Our findings suggest that the SIRT1 rs3758391 genetic polymorphism can affect platinum-based chemotherapy sensitivity in lung cancer patients, and SIRT1 may be act as a potential biomarker on lung cancer chemotherapy response.
Keywords:SIRT1  Single nucleotide polymorphism  Lung cancer  Chemosensitivity
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