CHEK2*1100delC homozygosity in the Netherlands-prevalence and risk of breast and lung cancer
European Journal of Human Genetics , Volume 22 - Issue 1 p. 46- 51
The 1100delC mutation in the CHEK2 gene has a carrier frequency of up to 1.5% in individuals from North-West Europe. Women heterozygous for 1100delC have an increased breast cancer risk (odds ratio 2.7). To explore the prevalence and clinical consequences of 1100delC homozygosity in the Netherlands, we genotyped a sporadic breast cancer hospital-based cohort, a group of non-BRCA1/2 breast cancer families, and breast tumors from a tumor tissue bank. Three 1100delC homozygous patients were found in the cohort of 1434 sporadic breast cancer patients, suggesting an increased breast cancer risk for 1100delC homozygotes (odds ratio 3.4, 95% confidence interval 0.4-32.6, P=0.3). Another 1100delC homozygote was found in 592 individuals from 108 non-BRCA1/2 breast cancer families, and two more were found after testing 1706 breast tumors and confirming homozygosity on their wild-type DNA. Follow-up data was available for five homozygous patients, and remarkably, three of them had developed contralateral breast cancer. A possible relationship between 1100delC and lung cancer risk was investigated in 457 unrelated lung cancer patients but could not be confirmed. Due to the small number of 1100delC homozygotes identified, the breast cancer risk estimate associated with this genotype had limited accuracy but is probably higher than the risk in heterozygous females. Screening for CHEK2 1100delC could be beneficial in countries with a relatively high allele frequency.European Journal of Human Genetics advance online publication, 8 May 2013; doi:10.1038/ejhg.2013.85.
|European Journal of Human Genetics|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Huijts, P, Hollestelle, A, Balliu, B, Houwing-Duistermaat, J.J, Meijers, J.C.M, Blom, J, … van Asperen, C.J. (2014). CHEK2*1100delC homozygosity in the Netherlands-prevalence and risk of breast and lung cancer. European Journal of Human Genetics, 22(1), 46–51. doi:10.1038/ejhg.2013.85