The Pathology Research Core (PRC) provides high quality histology-related services, performed within a quality system based on CLIA standards, including preparation of microscopy slides, tissue microarray construction, immunostaining, digital image capture and analysis, laser capture microdissection, and preparation of tissues for subsequent nucleic acid or protein extraction. Most services are performed using clinical diagnostic tissues, allowing Mayo Clinic Cancer Center (MCCC) investigators to take advantage of the wealth of clinical materials for biomarker discovery and validation. PRC is a critical asset in the translation of basic biology to clinical relevance by MCCC members. The Shared Resource Advisory Committee-B reviews with the PRC Director the operations, fee structure, budget, utilization, and user-satisfaction on an annual basis. MCCC leadership works with the Institutional Research Core Subcommittee to provide financial support to PRC. Dr. Flotte has 30 years' experience with research pathology as an NIH funded investigator and as research laboratory director. He has been a principal investigator, a pathology core director, space committee chair, and SPORE executive committee member. The PRC supervisor has a 4-year college degree in molecular biology and extensive management training courses through Mayo Office of Leadership and Organization Development. In 2012, PRC completed 1,122 requests for work from 173 users, 116 (67%) of whom were MCCC members. Fifty-one members had peer-reviewed support. Access to services provided by PRC is open to all Mayo investigators, including MCCC members, on a first come, first served basis. Chargebacks are structured to ensure that federally funded Mayo investigators, including MCCC members, have the lowest rates, as is required by federal regulations. Antibody optimization is fully subsidized by the MCCC for Cancer Center members. In comparison of PRC rates with 5 other academic institutions, PRC rates are significantly less than average for 9 of 11 services and within range for the other 2 services. Hours of operation are from 7:00 am to 6:00 pm Monday through Friday. Work requests can be submitted electronically at any time. Technical staff includes 9 FTE. The PRC is now located at MCR, MCA, and MCF.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA015083-42
Application #
9097581
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2016-03-01
Budget End
2017-02-28
Support Year
42
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Lu, Yingchang; Beeghly-Fadiel, Alicia; Wu, Lang et al. (2018) A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk. Cancer Res 78:5419-5430
Dasari, Surendra; Newsom, Sean A; Ehrlicher, Sarah E et al. (2018) Remodeling of skeletal muscle mitochondrial proteome with high-fat diet involves greater changes to ?-oxidation than electron transfer proteins in mice. Am J Physiol Endocrinol Metab 315:E425-E434
Nowsheen, Somaira; Aziz, Khaled; Aziz, Asef et al. (2018) L3MBTL2 orchestrates ubiquitin signalling by dictating the sequential recruitment of RNF8 and RNF168 after DNA damage. Nat Cell Biol 20:455-464
Razidlo, Gina L; Burton, Kevin M; McNiven, Mark A (2018) Interleukin-6 promotes pancreatic cancer cell migration by rapidly activating the small GTPase CDC42. J Biol Chem 293:11143-11153
Wu, Dongyan; Yang, Haitao; Winham, Stacey J et al. (2018) Mediation analysis of alcohol consumption, DNA methylation, and epithelial ovarian cancer. J Hum Genet 63:339-348
Leon-Ferre, Roberto A; Polley, Mei-Yin; Liu, Heshan et al. (2018) Impact of histopathology, tumor-infiltrating lymphocytes, and adjuvant chemotherapy on prognosis of triple-negative breast cancer. Breast Cancer Res Treat 167:89-99
Jahanseir, Khadijeh; Xing, Deyin; Greipp, Patricia T et al. (2018) PDGFB Rearrangements in Dermatofibrosarcoma Protuberans of the Vulva: A Study of 11 Cases Including Myxoid and Fibrosarcomatous Variants. Int J Gynecol Pathol 37:537-546
Painter, Jodie N; O'Mara, Tracy A; Morris, Andrew P et al. (2018) Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Med 7:1978-1987
Yu, Jia; Qin, Bo; Moyer, Ann M et al. (2018) DNA methyltransferase expression in triple-negative breast cancer predicts sensitivity to decitabine. J Clin Invest 128:2376-2388
Sugihara, Takaaki; Werneburg, Nathan W; Hernandez, Matthew C et al. (2018) YAP Tyrosine Phosphorylation and Nuclear Localization in Cholangiocarcinoma Cells Are Regulated by LCK and Independent of LATS Activity. Mol Cancer Res 16:1556-1567

Showing the most recent 10 out of 1129 publications