The purpose of the Animal Model and Therapeutics Evaluation Core (AMTEC) is to enhance the peer reviewed funded research activities of KCI members whose research needs involve the use of animal models. Our goal is to provide expert scientific consultation, technical expertise and access to a wide breadth of relevant tumor models and associated animal-related services. AMTEC is grouped in the Basic Research Core Cluster which, in addition to AMTEC, includes the Proteomics Core and the Microscopy, Imaging and Cytometry Resources Core (MICR). Established in 2012, the services provided by the AMTEC Core have already contributed to 14 peer-reviewed publications. AMTEC maintains and distributes cancer models and authenticated cell lines originally developed at KCI; conducts in vivo testing of novel therapeutics; and assists investigators in many aspects of small animal research. AMTEC also makes it easier for an investigator to utilize other appropriate cores for follow-up analysis, i.e. provides assistance with administration of anesthesia, study drugs, contrast agents and radioactive tracers, to post?procedure recovery and health care monitoring for small animal imaging; and generates in vivo derived tissues and samples for analysis in the Proteomics, Biobanking and Correlative Sciences (BCS), Pharmacology and Genomics Cores. Core operations are currently centered within the conveniently located Prentis Cancer Research Building animal facility, allowing AMTEC personnel to be within two-three blocks of the primary laboratory locations of most Cancer Center members and all on-site animal studies. Our resources include barrier animal holding rooms for immuno-compromised or transgenic mice, and biosafety Level-2 areas for carcinogen and chemotherapeutic experiments, manipulations and necropsy. Each AMTEC staff member has extensive small animal expertise (with a minimum 25 years of training and experience) and possesses a high level of proficiency in small animal techniques and procedures. Core staff members have not only successfully completed all Institutional Animal Care and Use Committee (IACUC) mandated small animal and surgery training courses; they also possess on-site certifications to handle radioactive materials, blood-borne pathogens, hazardous agents and operate x-ray generating equipment. Certifications are reviewed and updated annually and supplemented with ongoing ad-hoc training to expand expertise in various techniques and procedures so that AMTEC can knowledgeably and competently assist Cancer Center members with design and execution of their in vivo studies. A major strength of AMTEC is the extensive expertise in testing novel therapeutic agents in syngeneic and xenogeneic tumor systems. All animal work is carried out solely under protocols approved by the IACUC and upon completion of animal care training. AMTEC can also augment and assist investigators in meeting these requirements and in developing competent proficiency.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA022453-37
Application #
9605738
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
37
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Wayne State University
Department
Type
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Su, Yongwei; Li, Xinyu; Ma, Jun et al. (2018) Targeting PI3K, mTOR, ERK, and Bcl-2 signaling network shows superior antileukemic activity against AML ex vivo. Biochem Pharmacol 148:13-26
Bonomi, Robin; Popov, Vadim; Laws, Maxwell T et al. (2018) Molecular Imaging of Sirtuin1 Expression-Activity in Rat Brain Using Positron-Emission Tomography-Magnetic-Resonance Imaging with [18F]-2-Fluorobenzoylaminohexanoicanilide. J Med Chem 61:7116-7130
Paximadis, Peter; Beebe-Dimmer, Jennifer L; George, Julie et al. (2018) Comparing Treatment Strategies for Stage I Small-cell lung Cancer. Clin Lung Cancer 19:e559-e565
Modi, Dipenkumar; Al-Kadhimi, Zaid; Chen, Wei et al. (2018) A phase II study of tacrolimus and thymoglobulin as graft-versus-host-disease prophylaxis in related donor allogeneic hematopoietic cell transplantation. Am J Hematol 93:E96-E98
Patki, Mugdha; McFall, Thomas; Rosati, Rayna et al. (2018) Chronic p27Kip1 Induction by Dexamethasone Causes Senescence Phenotype and Permanent Cell Cycle Blockade in Lung Adenocarcinoma Cells Over-expressing Glucocorticoid Receptor. Sci Rep 8:16006
Teslow, Emily A; Bao, Bin; Dyson, Greg et al. (2018) Exogenous IL-6 induces mRNA splice variant MBD2_v2 to promote stemness in TP53 wild-type, African American PCa cells. Mol Oncol 12:1138-1152
Rathinam, Rajamani; Rosati, Rita; Jamesdaniel, Samson (2018) CRISPR/Cas9-mediated knockout of Lim-domain only four retards organ of Corti cell growth. J Cell Biochem 119:3545-3553
Munkanatta Godage, Dhanushka N P; VanHecke, Garrett C; Samarasinghe, Kusal T G et al. (2018) SMYD2 glutathionylation contributes to degradation of sarcomeric proteins. Nat Commun 9:4341
Han, Jing; Li, Yue; Liu, Xiuli et al. (2018) Metformin suppresses retinal angiogenesis and inflammation in vitro and in vivo. PLoS One 13:e0193031
Kim, Seongho; Wong, Weng Kee (2018) Discussion on Optimal treatment allocations in space and time for on-line control of an emerging infectious disease. J R Stat Soc Ser C Appl Stat 67:778-779

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