Ye Yuanqing, Lippman Scott M, Lee J Jack, Chen Meng, Frazier Marsha L, Spitz Margaret R, Wu Xifeng
Department of Epidemiology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2008 Nov 1;113(9):2488-95. doi: 10.1002/cncr.23854.
Cell-cycle checkpoint controls regulate cell-cycle progression and proliferation. Alterations in cell-cycle control mechanisms are linked to tumorigenesis.
This case-control study included 147 cases and 147 controls. The authors used a pathway-based approach to assess the association between 10 potential functional single-nucleotide polymorphisms from 7 cell-cycle control genes and the risk of oral premalignant lesions (OPLs). They also used classification and regression tree analysis to examine high-order gene-gene and gene-smoking interactions.
Compared with the homozygous wild-type GG genotype of CCND1 P241P, individuals with the AG genotype exhibited an increased risk of OPL (odds ratio, 1.58; 95% confidence interval, 0.89-2.83), and carriers of the AA genotype had a significantly increased risk of OPL (odds ratio, 2.75; 95% confidence interval, 1.33-5.71), with risk increasing significantly with the increasing number of variant alleles (P= .006). The risk of OPL increased significantly as the number of unfavorable genotypes in the pathway increased (P= .002). The final decision tree in the classification and regression tree analysis contained 5 terminal nodes. Compared with the never smokers (the lowest risk group), the odds ratios for terminal nodes 2 through 5 ranged from 1.21 to 5.40.
The results illustrated the advantage of using a pathway-based approach for analyzing gene-gene and gene-smoking interactions. Specifically, the authors showed that genetic polymorphisms in cell-cycle control pathway genes may contribute to the risk of OPL.
细胞周期检查点控制调节细胞周期进程和增殖。细胞周期控制机制的改变与肿瘤发生有关。
本病例对照研究纳入了147例病例和147例对照。作者采用基于通路的方法来评估来自7个细胞周期控制基因的10个潜在功能性单核苷酸多态性与口腔癌前病变(OPL)风险之间的关联。他们还使用分类和回归树分析来研究高阶基因-基因和基因-吸烟相互作用。
与CCND1 P241P的纯合野生型GG基因型相比,AG基因型个体患OPL的风险增加(优势比,1.58;95%置信区间,0.89 - 2.83),AA基因型携带者患OPL的风险显著增加(优势比,2.75;95%置信区间,1.33 - 5.71),风险随着变异等位基因数量的增加而显著增加(P = 0.006)。随着通路中不利基因型数量的增加,OPL的风险显著增加(P = 0.002)。分类和回归树分析中的最终决策树包含5个终端节点。与从不吸烟者(风险最低组)相比,终端节点2至5的优势比范围为1.21至5.40。
结果说明了使用基于通路的方法分析基因-基因和基因-吸烟相互作用的优势。具体而言,作者表明细胞周期控制通路基因中的遗传多态性可能导致OPL的风险。