The DWPF: Results of full scale qualification runs leading to radioactive operations

The Defense Waste Processing Facility (DWPF) at the Savannah River Site in Aiken, SC will immobilize high-level radioactive liquid waste, currently stored in underground carbon steel tanks, in borosilicate glass. The radioactive waste is transferred to the DWPF in two forms: precipitate slurry and sludge slurry. The radioactive waste is pretreated and then combined with a borosilicate glass frit in the DWPF. This homogeneous slurry is fed to a Joule-heated melter which operates at approximately 1150 degrees C. The glass is poured into stainless steel canisters for eventual disposal in a geologic repository. The DWPF product (i.e. the canistered waste form) must comply with the Waste Acceptance Product Specifications (WAPS) in order to be acceptable for disposal. The DWPF has completed Waste Qualification Runs which demonstrate the facility`s ability to comply with the waste acceptance specifications. During the Waste Qualification Runs seventy-one canisters of simulated waste glass were produced in preparation for Radioactive Operations. These canisters of simulated waste glass were produced during five production campaigns which also exercised the facility prior to beginning Radioactive Operations. The results of the Waste Qualification Runs are presented

The effect on melanoma risk of genes previously associated with telomere length.

Telomere length has been associated with risk of many cancers, but results are inconsistent. Seven single nucleotide polymorphisms (SNPs) previously associated with mean leukocyte telomere length were either genotyped or well-imputed in 11108 case patients and 13933 control patients from Europe, Israel, the United States and Australia, four of the seven SNPs reached a P value under .05 (two-sided). A genetic score that predicts telomere length, derived from these seven SNPs, is strongly associated (P = 8.92x10(-9), two-sided) with melanoma risk. This demonstrates that the previously observed association between longer telomere length and increased melanoma risk is not attributable to confounding via shared environmental effects (such as ultraviolet exposure) or reverse causality. We provide the first proof that multiple germline genetic determinants of telomere length influence cancer risk.This is the final version of the article. It first appeared from Oxford University Press via http://dx.doi.org/10.1093/jnci/dju26

Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas

Although the MYC oncogene has been implicated in cancer, a systematic assessment of alterations of MYC, related transcription factors, and co-regulatory proteins, forming the proximal MYC network (PMN), across human cancers is lacking. Using computational approaches, we define genomic and proteomic features associated with MYC and the PMN across the 33 cancers of The Cancer Genome Atlas. Pan-cancer, 28% of all samples had at least one of the MYC paralogs amplified. In contrast, the MYC antagonists MGA and MNT were the most frequently mutated or deleted members, proposing a role as tumor suppressors. MYC alterations were mutually exclusive with PIK3CA, PTEN, APC, or BRAF alterations, suggesting that MYC is a distinct oncogenic driver. Expression analysis revealed MYC-associated pathways in tumor subtypes, such as immune response and growth factor signaling; chromatin, translation, and DNA replication/repair were conserved pan-cancer. This analysis reveals insights into MYC biology and is a reference for biomarkers and therapeutics for cancers with alterations of MYC or the PMN. We present a computational study determining the frequency and extent of alterations of the MYC network across the 33 human cancers of TCGA. These data, together with MYC, positively correlated pathways as well as mutually exclusive cancer genes, will be a resource for understanding MYC-driven cancers and designing of therapeutics