摘要
本文对等位基因特异性PCR(Alelespecific,AS)和多重差别(Multiplexdiferential,MD)PCR技术进行了优化,并用此法联合检测了105例江苏地区健康人群及68例肺癌患者CYP1A1、GSTM1的等位基因型。结果表明:ASPCR及MDPCR采用的设立双参照扩增体系,可一次同时检测CYP1A1和GSTM1的等位基因型。在肺癌患者组中,CYP1A1的突变型Val/Val的频率12/68(17.6%)约为健康组9/105(8.57%)的205倍,而GSTM1纯合缺失的频率,肺癌组为39/68(573%),与健康对照组42/105(40%)相比,亦有显著增加(P<0.05)。
Allelespecific PCR(ASPCR) and multiplex differential PCR (MDPCR) were used to identify the genotypes of CYP1A1 and GSTM1 in 68 lung cancer patients and 105 healthy controls. The results showed that genotypes of CYP1A1 and GSTM1 could be detected simultaneously with ASPCR and MDPCR; The frequency of CYP1A1Val/Val in lung cancer patients group was 12/68(17.6%), about 2.05fold than that in healthy controls 9/105(8.57%), and the frequency of GSTM1 0/0 was 39/68(57.4%), remarkably higher compared with 42/105(40%) in healthy controls ( P <0.05)
出处
《癌变.畸变.突变》
CAS
CSCD
1999年第3期119-122,共4页
Carcinogenesis,Teratogenesis & Mutagenesis
基金
江苏省卫生厅科研基金