摘要
目的:研究乳腺癌化疗患者CYP3A4*1G基因多态性与紫杉醇血药浓度的关系。方法:采用高效液相色谱(HPLC)法测定紫杉醇血药浓度,以聚合酶链式反应-限制性片段长度多态性法(PCR-RFLP)检测CYP3A4*1G基因多态性,探讨使用紫杉醇化疗患者CYP3A4*1G基因型与紫杉醇血药浓度的关系。结果:不同基因型患者紫杉醇血药浓度分别为:CC型(0.097 6±0.042 9)μg/ml、CT型(0.102 4±0.046 6)μg/ml、TT型(0.106 5±0.036 7)μg/ml。3种基因型之间,紫杉醇血药浓度差异无统计学意义(P>0.05)。结论:CYP3A4*1G基因突变对紫杉醇血药浓度无影响。
OBJECTIVE:To investigate the relationship between the genetic polymorphism of CYP3A4*1G and the plasma concentrations of Paclitaxel in the chemotherapy patients with breast cancer. METHODS:The plasma concentrations of paclitaxel were detected with high performance liquid chromatography(HPLC),and the genetic polymorphism of CYP3A4*1G was determined using polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) to analysis the relationship between the genotypes of CYP3A4*1G and the plasma concentrations of paclitaxel in the chemotherapy patients with breast cancer. RESULTS:The plasma concentrations of paclitaxel in patients with different genotypes were CC allele(0.097 6±0.042 9)μg/ml,CT allele(0.102 4±0.046 6)μg/ml and TT allele(0.106 5±0.036 7)μg/ml. There were no significant differences of the plasma concentrations of paclitaxel among these 3 genotypes(P〉0.05). CONCLUSION:There are no relation between the gene mutation of CYP3A4*1G and the plasma concentrations of Paclitaxel.
出处
《中国药房》
CAS
北大核心
2015年第8期1063-1065,共3页
China Pharmacy
基金
黑龙江省教育厅2013年度科学技术研究项目(No.12531683)