Trace Elements (TE) Shared Resource The Trace Element (TE) Shared Resource is a specialized facility dedicated to determining trace element concentration, and form of trace elements, in a wide variety of biological and environmental media. The chemistry of inorganic elements inextricably is linked with the study of cancer. Whether determining the fate and effects of known carcinogens (such as arsenic), the potential antagonistic effects of elements (such as selenium), or the therapeutic effects of platinum or Fe nanoparticles, there is a clear need for routine advanced trace element analytical methods to support cancer research. The critical nature of these services for the Norris Cotton Cancer Center (NCCC) research program has led to designation of TE as an NCCC-supported Shared Resource and to a request for future CCSG funding. In the TE core, Inductively Coupled Plasma Mass Spectrometry (ICP-MS) methodologies have been developed to provide analysis of trace metals in solids, solution, blood, and toenails. TE services include arsenic speciation in solutions, mercury speciation in solution, and ICP-MS tuning and operation for routine analysis. There have been notable examples of cancer research using TE resources. For example, the TE core developed innovative methods for determining Arsenic species in rice, juice, and toddler formulae. Also TE-developed spatial analyses show the distribution of a trace element within tissue sections, which is determined 'in situ' at pre-determined resolution, creating a 2-dimensional elemental image map from biological thin sections using laser ablation-ICP-MS. Using this technology, the TE core developed methods for detecting Fe, Cu, and Zn in rat brain sections. Analytical expertise is provided by the TE Core Director and a staff consisting of a PhD level scientist and an advanced Research Technician. The TE core has collaborated with NCCC researchers in 5 of the NCCC Programs (Cancer Epidemiology, Cancer Mechanisms, Molecular Therapeutics, Cancer Imaging & Radiobiology, and Immunology & Cancer Immunotherapy) to determine the concentration or form of trace elements in biological samples.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA023108-39
Application #
9404358
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2017-12-01
Budget End
2018-11-30
Support Year
39
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
Ji, Xuemei; Bossé, Yohan; Landi, Maria Teresa et al. (2018) Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nat Commun 9:3221
Ferreiro-Iglesias, Aida; Lesseur, Corina; McKay, James et al. (2018) Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity. Nat Commun 9:3927
Bronson, Mackenzie R; Kapadia, Nirav S; Austin, Andrea M et al. (2018) Leveraging Linkage of Cohort Studies With Administrative Claims Data to Identify Individuals With Cancer. Med Care 56:e83-e89
Gorlov, Ivan; Orlow, Irene; Ringelberg, Carol et al. (2018) Identification of gene expression levels in primary melanoma associated with clinically meaningful characteristics. Melanoma Res 28:380-389
Hancock, D B; Guo, Y; Reginsson, G W et al. (2018) Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Mol Psychiatry 23:1-9
Li, Yafang; Xiao, Xiangjun; Han, Younghun et al. (2018) Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis 39:336-346
Wu, Wenting; 23andMe Research Team; Amos, Christopher I et al. (2018) Inverse Relationship between Vitiligo-Related Genes and Skin Cancer Risk. J Invest Dermatol 138:2072-2075
Downey-Kopyscinski, Sondra; Daily, Ellen W; Gautier, Marc et al. (2018) An inhibitor of proteasome ?2 sites sensitizes myeloma cells to immunoproteasome inhibitors. Blood Adv 2:2443-2451
Shiner, Brian; Westgate, Christine Leonard; Gui, Jiang et al. (2018) A Retrospective Comparative Effectiveness Study of Medications for Posttraumatic Stress Disorder in Routine Practice. J Clin Psychiatry 79:
Patel, Mickey V; Shen, Zheng; Wira, Charles R (2018) Poly (I:C) and LPS induce distinct immune responses by ovarian stromal fibroblasts. J Reprod Immunol 127:36-42

Showing the most recent 10 out of 1911 publications