Tag Archives: EBR2A

The 1100delC mutation in the gene includes a carrier frequency of

The 1100delC mutation in the gene includes a carrier frequency of up to 1. data was available for five homozygous patients and three of them had developed contralateral breast tumor remarkably. A possible romantic relationship between 1100delC and lung tumor risk was looked into in 457 unrelated lung tumor individuals but cannot be confirmed. Because of the few 1100delC homozygotes determined the breasts EBR2A cancer risk estimation connected with this genotype got limited precision but is most likely higher than the chance in heterozygous females. Testing for 1100delC could possibly be beneficial in countries with a higher allele frequency relatively. gene on chromosome 22 can be a tumor-suppressor gene encoding the proteins kinase CHEK2 which can be involved with cell-cycle control and DNA restoration in response to DNA double-strand breaks.1 2 3 A deletion of the cytosine at placement 1100 (1100delC) in are available in individuals from North-West European countries having a heterozygous carrier frequency as high as 1.5% in a few populations. In additional geographical areas the mutation is a lot rarer or absent even.3 4 5 The 1100delC frameshift mutation causes a early prevent codon which activates nonsense-mediated decay producing a lower expression of mRNA in heterozygous carriers.6 7 8 Although a minimal degree of mutant mRNA continues to FTY720 be detectable the current presence of the mutated FTY720 proteins cannot be demonstrated in lymphoblastoid cell lines from human beings heterozygous for the 1100delC mutation.9 Heterozygous female carriers from the 1100delC mutation possess an increased breasts cancer risk with an odds ratio (OR) of 2.7 (95% confidence interval (95% CI): 2.1-3.4) in sporadic breasts cancer instances and an OR of 4.8 (95% CI: 3.3-7.2) in familial breasts cancer instances.3 10 11 FTY720 12 13 Breasts cancer individuals heterozygous for 1100delC likewise have an increased threat of developing contralateral breasts cancer in comparison to wild-type breasts cancer individuals.5 13 14 15 16 17 18 19 20 The contralateral breast cancer risk may be even higher when radiotherapy has been given to treat the first tumor.15 19 It must be noted that in women FTY720 who also carry a pathogenic mutation the 1100delC allele does not seem to modify breast cancer risk.3 14 21 An association of the 1100delC allele with increased colon cancer and prostate cancer risk has been described while an association with melanoma could not be found.22 23 24 25 Other variants in have been associated with lung cancer but a possible association of 1100delC with lung cancer has never been investigated.26 27 28 29 30 31 Homozygosity for 1100delC is expected to be rare and until recently there had only been two reports on homozygous carriers a male who developed colon cancer at age 52 years32 and a female who developed bilateral breast cancer at ages 47 and 61 years and uterine sarcoma at age 58 years.33 Recently Adank breast cancer families.11 The phenotypes of homozygous 1100delC carriers were studied. Materials and methods Cohorts The ORIGO cohort is a Dutch hospital-based cohort of 1434 breast cancer patients diagnosed with a first primary breast cancer between 1996 and 2005 in two academic hospitals in the South-West area of the Netherlands.17 35 Patients FTY720 were included regardless of family history of breast cancer. Average age at diagnosis was 53.4 years (SD 11.2 years). A subset of the ORIGO cohort had been genotyped for the 1100delC mutation before17 but with a genotyping technique that precluded the identification of homozygous 1100delC individuals. Female family members (breast cancer families (range 1-24 individuals per family) were ascertained through the Departments of Clinical Genetics in Leiden Rotterdam and Nijmegen as well as through the Netherlands Foundation for the Detection of Hereditary Tumors. Families were included if there were at least three cases of breast cancer diagnosed before the age of 60 years from whom genotypes could be determined or could be inferred by genotyping close relatives. Mutations in or were excluded in these families as described previously.11 A total of 325 affected and 267 unaffected females were genotyped for the 1100delC mutation. The Rotterdam Medical Oncology Tumorbank (RMOT) has been described previously.36 37 DNA samples from 1706 breast tumor specimens from the three study cohorts were available for analysis. The first series of 503 samples was drawn from a consecutive series of unselected breast cancer cases diagnosed in the year 1990 median age at diagnosis of these cases was 62.1 years (range 22.7-89.6 years). The second.