Trace Elements The chemistry of inorganic elements is linked inextricably with the study of cancer. This is especially true for our catchment area, given the high level of inorganic element exposures typical of ?the Granite State?. Whether studying known carcinogens, such as arsenic, the potential antagonistic effects of elements, such as selenium, or the therapeutic uses of platinum or iron nanoparticles, there is a clear need for both routine and advanced trace element analytical methods to support NCCC research. The Trace Elements (TE) Shared Resource provides access to low-level inorganic elemental analysis to all four research programs within the Cancer Center. TE uses state-of-the-art ICP-MS instruments to quantify multiple elements and, when coupled with chromatography, multiple contaminant compounds (species) in a variety of biological and environmental media. Cutting-edge ICP-MS instrumentation (e.g., triple-quadrupole ICP-QQQ) provides rapid, interference- free analysis of established and emerging contaminants and macro- and micro-nutrient elements. The breadth of sample types handled by TE spans water, soil, sediment, invertebrates, fish and animal tissues and organs, cell lysates, human hair, toenail, blood, urine, placenta, foodstuffs, and beverages. The ability to handle such a broad array of sample types is a unique feature of TE. In some cases, the sample mass available for analysis is <10 mg, and methods often are adapted to account for small sample masses on a case-by-case basis. Analytical data must be collected according to accepted protocols for sample preparation, analysis, and quality control. TE has established protocols and a Quality Assurance program, uses methods based on those of the CDC, FDA, EPA, and USGS; and participates in national and international proficiency testing programs to ensure accurate, precise, and defensible data. TE has very strong links to the Cancer Population Sciences (CPS) Program. TE is an internationally-recognized center for low-level analysis of chemical elements and their compounds in biological tissues. TE has provided services for 27 other US academic institutions over the past funding cycle and fulfills a unique niche in providing state-of-the-art analytical services in trace elemental analysis. Over the last funding cycle, TE has run 6,721 samples for 12 NCCC Members from all 4 NCCC Programs (CPS [1], CBT [1], ICI [2], and TEC [8]). Funded NCCC Members have represented 15% (10) of Total Users, and we are requesting only 3% of the Total TE Budget from CCSG support. One focus of the CPS Program is early life exposure to arsenic, and TE is integral to the determination and speciation of arsenic for this project. This work has directly informed state and national public health policy. For example, the US FDA announced a proposed limit for inorganic arsenic in infant cereal of 100 ppb in 2016. For the TEC Program, TE provided a method for measuring iron nanoparticles in animal tissue. TE has contributed to CBT investigators monitoring the therapeutic effects of platinum. TE is demonstrably an essential, efficient and high-impact resource that continues to play a pivotal role in NCCC research.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA023108-41
Application #
9855311
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
41
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Soneji, Samir S; Sung, Hai-Yen; Primack, Brian A et al. (2018) Quantifying population-level health benefits and harms of e-cigarette use in the United States. PLoS One 13:e0193328
Durand, Marie-Anne; Yen, Renata West; O'Malley, A James et al. (2018) What matters most: protocol for a randomized controlled trial of breast cancer surgery encounter decision aids across socioeconomic strata. BMC Public Health 18:241
Molodtsov, Aleksey; Turk, Mary Jo (2018) Tissue Resident CD8 Memory T Cell Responses in Cancer and Autoimmunity. Front Immunol 9:2810
Courtney, Andrea L; Rapuano, Kristina M; Sargent, James D et al. (2018) Brain Reward Responses Are Behaviorally Relevant: The Authors Respond. J Stud Alcohol Drugs 79:41-42
Tosteson, Anna N A; Yang, Qian; Nelson, Heidi D et al. (2018) Second opinion strategies in breast pathology: a decision analysis addressing over-treatment, under-treatment, and care costs. Breast Cancer Res Treat 167:195-203
Lin, Anping; Yin, Juan; Cheng, Chao et al. (2018) Decreased expression of FOXA2 promotes eutopic endometrial cell proliferation and migration in patients with endometriosis. Reprod Biomed Online 36:181-187
Elder, David E; Piepkorn, Michael W; Barnhill, Raymond L et al. (2018) Pathologist characteristics associated with accuracy and reproducibility of melanocytic skin lesion interpretation. J Am Acad Dermatol 79:52-59.e5
Rutter, Carolyn M; Kim, Jane J; Meester, Reinier G S et al. (2018) Effect of Time to Diagnostic Testing for Breast, Cervical, and Colorectal Cancer Screening Abnormalities on Screening Efficacy: A Modeling Study. Cancer Epidemiol Biomarkers Prev 27:158-164
Kumar, Nishant; Tafe, Laura J; Higgins, John H et al. (2018) Identifying Associations between Somatic Mutations and Clinicopathologic Findings in Lung Cancer Pathology Reports. Methods Inf Med 57:63-73
Punshon, Tracy; Jackson, Brian P (2018) Essential micronutrient and toxic trace element concentrations in gluten containing and gluten-free foods. Food Chem 252:258-264

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