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. 2010 Feb;3(2):246-53.
doi: 10.1158/1940-6207.CAPR-08-0228. Epub 2010 Jan 19.

The six-nucleotide deletion/insertion variant in the CASP8 promoter region is inversely associated with risk of squamous cell carcinoma of the head and neck

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The six-nucleotide deletion/insertion variant in the CASP8 promoter region is inversely associated with risk of squamous cell carcinoma of the head and neck

Chunying Li et al. Cancer Prev Res (Phila). 2010 Feb.

Abstract

Caspase 8 (CASP8) is an apoptosis-related cysteine peptidase involved in the death receptor pathway and likely in the mitochondrial pathway. A CASP8 promoter region six-nucleotide deletion/insertion (-652 6N ins/del) variant and a coding region D302H polymorphism are reportedly important in cancer development, but no reported study has assessed the associations of these genetic variations with risk of head and neck cancer. In a hospital-based study of non-Hispanic whites, we genotyped CASP8 -652 6N del and 302H variants in 1,023 patients with squamous cell carcinoma of the head and neck (SCCHN) and 1,052 cancer-free controls. Crude and adjusted odds ratios (OR) and 95% confidence intervals (CI) were estimated using unconditional logistic regression models. The CASP8 -652 6N del variant genotypes or haplotypes were inversely associated with SCCHN risk (adjusted OR, 0.70; 95% CI, 0.57-0.85 for the ins/del + del/del genotypes compared with the ins/ins genotype; adjusted OR, 0.73; 95% CI, 0.55-0.97 for the del-D haplotype compared with the ins-D haplotype). Furthermore, the number of the CASP8 -652 6N del (but not 302H) variant allele tended to correlate with increased levels of camptothecin-induced p53-mediated apoptosis in T lymphocytes from 170 cancer-free controls. We concluded that the CASP8 -652 6N del variant allele may contribute to the risk of developing SCCHN in non-Hispanic white populations. Further validation by population-based case-control studies and rigorous mechanistic studies is warranted.

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Figure 1
Figure 1. Graphic presentation of apoptotic index by age and CASP8 genotypes
A, Scatter plot for correlation between apoptotic index (%) and age of 170 cancer-free subjects: the apoptotic index increases as age increases. B, Boxplot for apoptotic index by CASP8 H302D genotypes: there is no trend of decreased apoptotic index as the number of the variant C allele increases. C, Boxplot for apoptotic index by CASP8 -652 6N genotypes: these is an insignificant trend of increased apoptotic index as the number of the D (deletion) allele increased, which is consistent with its observed inverse association, assuming the lymphocytes serve as the surrogates for target cells.

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