DNA was genotyped using GeneChip Human Mapping 500 K Arrays or Genome-Wide Human SNP Arrays 6.0. To increase genomic coverage, genotypes of additional SNPs were imputed using data from HapMap Phase II. After quality control filtering of genotype data, 1367 cases (9 men) and 1658 controls (1156 men) were analyzed on a total of 2,067,645 SNPs. Results: Overall, 33 genomic regions (67 candidate SNPs) were associated with breast cancer Androgen Receptor Antagonist libraries risk at the p smaller than 10(-6) level. Twenty of these regions contained defined genes, including one already associated with breast cancer risk: TOX3.

With a lower threshold for preliminary significance to p smaller than 10(-5), we identified 11 additional SNPs in FGFR2, a well-established breast cancer-associated gene. Ten candidate SNPs were selected, excluding those already associated with breast cancer, for technical validation as well as replication in 1668 samples from the same ON-01910 price population. Only SNP rs345299, located in intron 1 of VAV3, remained suggestively associated (p-value, 1.16×10(-5)), but it did not associate with breast cancer risk in pooled data from two large, mixed-population cohorts. Conclusions: This study indicated the role of TOX3 and FGFR2 as breast cancer susceptibility genes in BRCA1/2-wild-type

breast cancer patients from Sardinian population.”
“To see more better understand the relevance of environmental factors to the changing patterns of bone cancer subtypes, we examine the incidence of osteosarcoma (OS), Ewing sarcoma (ES), and chondrosarcoma (CS) using data from cancer incidence in five continents. Age-specific and age-standardized incidence rates (ASRs) per 100,000 person-years were computed

and stratified by country (n = 43), subtype, and sex during 2003-2007. Temporal patterns of ASRs were examined during 1988-2007 (12 countries). Age-period-cohort models were fitted for the USA and UK by subtype. For most countries, OS represented 20-40 % of all bone cancers, ES smaller than 20 %, while CS proportions varied more considerably. Overall ASRs of bone cancers were 0.8-1.2/100,000 in men and 0.5-1.0 in women (0.20-0.35/100,000 for OS and 0.10-0.30/100,000 for CS in both men and women, and smaller than 0.10-0.25/100,000 in men and 0.05-0.25/100,000 in women for ES). The age-specific incidence rates revealed a bimodal peak of OS, one peak of ES in childhood, and a more heterogeneous pattern for CS. The overall bone cancer incidence trends are generally flat, but more heterogeneous for ES and CS. A declining OS incidence was observed in the UK and USA (men), an increase in CS in the UK and USA (female), and an apparent increase in ES, followed by a leveling off in successive US and UK cohorts.