BIOREPOSITORY AND MOLECULAR PATHOLOGY SHARED RESOURCE ABSTRACT The Biorepository and Molecular Pathology (BMP) Shared Resource, established in 2000, seamlessly integrates exceptional expertise in biorepository, histology, and molecular diagnostic services for research at Huntsman Cancer Institute (HCI). The College of American Pathologists (CAP)-accredited Biorepository Section provides researchers with high quality, richly annotated fresh tumor, blood, and other body fluids with patient-matched normal controls, using adept procurement, processing, storage, and prioritized distribution. The biorepository is responsible for managing patient consent and IRB approval. Data entry, searches, and annotation of biospecimens with pathology, electronic medical record, genealogical (via the Utah Population Database Shared Resource), genomic (via the High-Throughput Genomics and Bioinformatic Shared Resource), and tumor registry data are all provided via the itBioPath software system used by the BMP Shared Resource (and built by the Research Informatics Shared Resource). The Research Histology Section is separate from hospital histology, facilitating dedicated and rapid turnaround for research. Research Histology performs all manner of expert histology on Biorepository frozen and fixed human and animal tissues, including tissue microarray work, processing, frozen and paraffin sectioning, and special staining from a catalogue of over 175 immuno- and histochemical options. The Molecular Diagnostic Section provides an essential bridge from scientific discovery to patient trials prior to CLIA test certification. It uses biospecimens and histologic preparations from the other two BMP sections for nucleic acid isolation and genetic analysis via Sequenom MassArray and Illumina MiSeq technologies. Data are uploaded to GNomEx, HCI's centralized genomics database. The BMP Shared Resource is directed by Evin Gulbahce, MD, who oversees daily operations and provides essential, pathologist-specific expertise to the Resource. The BMP resides partially in the Cancer Hospital adjacent to pathology/operating rooms to facilitate rapid fresh tissue banking, with the Biorepository section on the third floor of the research building directly adjacent to laboratories. The BMP Shared Resource markedly advances efficiency and cost savings for cancer research at HCI, providing precious, highly annotated biospecimens, histology, and molecular diagnostics which add substantial value to HCI's research efforts and advance HCI?s goals to improve cancer diagnosis, treatment, and cure. The importance of the Resource is demonstrated by its wide array of users and its contributions to numerous publications. In 2013, use of the Resource by Cancer Center investigators with peer-reviewed funding exceeded 43%, while the CCSG budget request is only 6% ($61,944) of the total proposed budget.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA042014-28
Application #
9273912
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
28
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Vahrenkamp, Jeffery M; Yang, Chieh-Hsiang; Rodriguez, Adriana C et al. (2018) Clinical and Genomic Crosstalk between Glucocorticoid Receptor and Estrogen Receptor ? In Endometrial Cancer. Cell Rep 22:2995-3005
Gupta, Sumati; Albertson, Daniel; Gaston, David et al. (2018) Comprehensive Genomic Sequencing of Urothelial Tumors Identifies Rare SMARCB1 (INI-1)-Deficient Carcinomas of the Urinary System. Clin Genitourin Cancer 16:e373-e382
Yazdimamaghani, Mostafa; Moos, Philip J; Ghandehari, Hamidreza (2018) Global gene expression analysis of macrophage response induced by nonporous and porous silica nanoparticles. Nanomedicine 14:533-545
Al-Agha, Abdulmoein Eid; Ahmed, Ihab Abdulhamed; Nuebel, Esther et al. (2018) Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation. J Clin Endocrinol Metab 103:555-563
Petersen, Jenna; Koptiuch, Cathryn; Wu, Yelena P et al. (2018) Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis. Patient Educ Couns 101:2011-2017
Flack, Caralyn E; Parkinson, John S (2018) A zipped-helix cap potentiates HAMP domain control of chemoreceptor signaling. Proc Natl Acad Sci U S A 115:E3519-E3528
Pishas, Kathleen I; Drenberg, Christina D; Taslim, Cenny et al. (2018) Therapeutic Targeting of KDM1A/LSD1 in Ewing Sarcoma with SP-2509 Engages the Endoplasmic Reticulum Stress Response. Mol Cancer Ther 17:1902-1916
Blackburn, Brenna E; Ganz, Patricia A; Rowe, Kerry et al. (2018) Reproductive and gynecological complication risks among thyroid cancer survivors. J Cancer Surviv 12:702-711
Wu, Yelena P; Aspinwall, Lisa G; Nagelhout, Elizabeth et al. (2018) Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma. J Cancer Educ 33:774-781
Kim, Hyung-Seok; McKnite, Autumn; Xie, Yuanyuan et al. (2018) Fibronectin type III and intracellular domains of Toll-like receptor 4 interactor with leucine-rich repeats (Tril) are required for developmental signaling. Mol Biol Cell 29:523-531

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