The goal of the Tissue Core is to provide investigators in the Pancreas SPORE with high quality patient data,DNA, RNA, serum, circulating tumor cells, and pancreas tissues from pancreatic cancer patients, and tomake these resources available for future studies. The activities of the Tissue Core will be overseen underthe combined leadership of Dr. W. Lingle, Director of the TACMA and Co-Director of the BAP SharedResources of the Mayo Clinic Cancer Center, and Dr. T. Smyrk, anatomic pathologist. The activities of theTissue Core will be conducted in a way that does not compromise patient confidentiality, yet will be ascomprehensive as possible in the materials that are provided. The acquisition of human tissue andsubsequent cellular/molecular analysis of that tissue within the context of pathology and patient data are keyto many laboratory-based studies of cancer. The Mayo Clinic has a strong tradition of ethically sound supportof research that links tissue acquisition and patient data records. Paraffin embedded tissues, histologicalslides, and associated patient charts from surgeries performed since the first decade of the 1900's aremaintained in Mayo's Tissue Registry and the Mayo Archives. The Tissue and Cell Molecular Analysis(TACMA) Shared Resource of the Mayo Clinic Cancer Center is a resource of expertise and service forimmunohistochemistry, laser capture microdissection, tissue microarray preparation, and digital imaging.Likewise, the Biospecimen Accessioning and Processing (BAP) Shared Resource of the Mayo Clinic CancerCenter is the primary site of accessioning and standardized processing of blood, frozen tissue, and othernon-paraffin embedded specimens collected explicitly for research. New methodologies for biospecimencollection, processing, and analysis will be developed in the Tissue Core. These methodologies will beshared with other Mayo SPORE Tissue Cores and integrated with services offered by the BAP and TACMAShared Resources. Tissue Core activities will be closely coordinated with the newly formed ClinicalResearch Core and with the Biostatistics Core to provide seamless linkage of clinical annotations withresearch biospecimens. Core D will be integrated with the existing tissue-oriented Cancer Center sharedresources and the other scientific Cores in this SPORE in order to provide a coordinated, centralized,dedicated program for standardized collection, accessioning, processing, and evaluation of biospecimensand patient data from pancreatic cancer patients. Furthermore, the Tissue Core will make biospecimenscollected for this SPORE available to the pancreas cancer research community in order to stimulatetranslational research with the goal of improving prevention and treatment of pancreatic cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
2P50CA102701-06
Application #
7510940
Study Section
Special Emphasis Panel (ZCA1-GRB-I (M1))
Project Start
2008-07-01
Project End
2013-06-30
Budget Start
2008-07-01
Budget End
2009-08-31
Support Year
6
Fiscal Year
2008
Total Cost
$141,933
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Antwi, Samuel O; Fagan, Sarah E; Chaffee, Kari G et al. (2018) Risk of Different Cancers Among First-degree Relatives of Pancreatic Cancer Patients: Influence of Probands' Susceptibility Gene Mutation Status. J Natl Cancer Inst :
Cobo, Isidoro; Martinelli, Paola; Flández, Marta et al. (2018) Transcriptional regulation by NR5A2 links differentiation and inflammation in the pancreas. Nature 554:533-537
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
Chaker, Mahmoud; Minden, Audrey; Chen, Suzie et al. (2018) Rho GTPase effectors and NAD metabolism in cancer immune suppression. Expert Opin Ther Targets 22:9-17
Sugimoto, Motokazu; Farnell, Michael B; Nagorney, David M et al. (2018) Decreased Skeletal Muscle Volume Is a Predictive Factor for Poorer Survival in Patients Undergoing Surgical Resection for Pancreatic Ductal Adenocarcinoma. J Gastrointest Surg 22:831-839
Danai, Laura V; Babic, Ana; Rosenthal, Michael H et al. (2018) Altered exocrine function can drive adipose wasting in early pancreatic cancer. Nature 558:600-604
Paradise, Brooke D; Barham, Whitney; Fernandez-Zapico, Martín E (2018) Targeting Epigenetic Aberrations in Pancreatic Cancer, a New Path to Improve Patient Outcomes? Cancers (Basel) 10:
Hogan, Kelly A; Cho, Dong Seong; Arneson, Paige C et al. (2018) Tumor-derived cytokines impair myogenesis and alter the skeletal muscle immune microenvironment. Cytokine 107:9-17
Tarragó, Mariana G; Chini, Claudia C S; Kanamori, Karina S et al. (2018) A Potent and Specific CD38 Inhibitor Ameliorates Age-Related Metabolic Dysfunction by Reversing Tissue NAD+ Decline. Cell Metab 27:1081-1095.e10
Chini, Eduardo N; Chini, Claudia C S; Espindola Netto, Jair Machado et al. (2018) The Pharmacology of CD38/NADase: An Emerging Target in Cancer and Diseases of Aging. Trends Pharmacol Sci 39:424-436

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