cell-cycle pathway;
single-nucleotide polymorphisms;
oral premalignant lesion;
classification and regression tree analysis;
D O I:
10.1002/cncr.23854
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BACKGROUND. Cell-cycle checkpoint controls regulate cell-cycle progression and proliferation. Alterations in cell-cycle control mechanisms are linked to tumorigenesis. METHODS. 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 polymorphisins from 7 cell-cycle control genes and the risk of oral premalignant lesions (OPLs). They also used classification zinc regression tree analysis to examine high-order gene-gene and gene-smoking interactions. RESULTS. 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 Further 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 snickers (the lowest risk group), the odds ratios for terminal nodes 2 through 5 ranged from 1.21 to 5.40. CONCLUSIONS. The results illustrated the advantage of using it pathway-based approach for analyzing gene-gene and gene-smoking interactions. Specifically, the authors showed that genetic polymorphisms in cell-cycle control pathway genes InaV contribute to the risk of OPL. Cancer 2008; 113:2488-95. (C) 2008 American Cancer Society.
机构:
Hutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Ch'ng, Sydney
;
Sullivan, Michael
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机构:
Christchurch Sch Med & Hlth Sci, Childrens Canc Res Grp, Christchurch, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Sullivan, Michael
;
Yuan, Lan
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h-index: 0
机构:
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Yuan, Lan
;
Davis, Paul
论文数: 0引用数: 0
h-index: 0
机构:
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Davis, Paul
;
Tan, Swee T.
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h-index: 0
机构:
Hutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
机构:
Hutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Ch'ng, Sydney
;
Sullivan, Michael
论文数: 0引用数: 0
h-index: 0
机构:
Christchurch Sch Med & Hlth Sci, Childrens Canc Res Grp, Christchurch, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Sullivan, Michael
;
Yuan, Lan
论文数: 0引用数: 0
h-index: 0
机构:
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Yuan, Lan
;
Davis, Paul
论文数: 0引用数: 0
h-index: 0
机构:
Wellington Sch Med & Hlth Sci, Dept Med, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand
Davis, Paul
;
Tan, Swee T.
论文数: 0引用数: 0
h-index: 0
机构:
Hutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New ZealandHutt Hosp, Wellington Reg Plast Maxillofacial & Burns Unit, Wellington, New Zealand