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Pharmacology Shared Resource

$204,344P30FY2016CANIH

Mayo Clinic Rochester, Rochester MN

Investigators

Linked publications, trials & patents

Trial NCT06508463Trial NCT06387979Trial NCT06381154Trial NCT06353191Trial NCT06315595Trial NCT06271291Trial NCT06238648Trial NCT06207188Trial NCT06160206Trial NCT06115772Trial NCT06078709Trial NCT06075524Trial NCT06073951Trial NCT06058663Trial NCT05917145Trial NCT05910801Trial NCT05720624Trial NCT05717153Trial NCT05704283Trial NCT05703399Trial NCT05674123Trial NCT05653661Trial NCT05640765Trial NCT05612100Trial NCT05591092Trial NCT05584449Trial NCT05575440Trial NCT05560009Trial NCT05557877Trial NCT05556525Trial NCT05549661Trial NCT05547386Trial NCT05547347Trial NCT05541016Trial NCT05530759Trial NCT05526417Trial NCT05523154Trial NCT05518903Trial NCT05512767Trial NCT05507879Trial NCT05507541Trial NCT05497804Trial NCT05465954Trial NCT05465941Trial NCT05447923Trial NCT05447910Trial NCT05443971Trial NCT05438563Trial NCT05417867Trial NCT05416983Trial NCT05412953Trial NCT05411523Trial NCT05411497Trial NCT05410977Trial NCT05407038Trial NCT05407025Trial NCT05403580Trial NCT05399004Trial NCT05393713Trial NCT05392946Trial NCT05388877Trial NCT05388851Trial NCT05388058Trial NCT05388006Trial NCT05356897Trial NCT05294367Trial NCT05288062Trial NCT05269381Trial NCT05246670Trial NCT05232851Trial NCT05224271Trial NCT05222620Trial NCT05212428Trial NCT05199285Trial NCT05194293Trial NCT05176223Trial NCT05168163Trial NCT05130060Trial NCT05112627Trial NCT05112614Trial NCT05111314Trial NCT05077735Trial NCT05075980Trial NCT05053100Trial NCT05045066Trial NCT05033288Trial NCT05030298Trial NCT05018208Trial NCT05005182Trial NCT04999826Trial NCT04975516Trial NCT04967196Trial NCT04926948Trial NCT04925817Trial NCT04917744Trial NCT04906369Trial NCT04897009Trial NCT04895735Trial NCT04892277Trial NCT04892264

Abstract

The Developmental Therapeutics Program, an established program of the Cancer Center, contributes to more effective treatment of malignant disease through e spectrum of basic end translational research. The AIMS ere to 1) define cellular pathways involved in survival end proliferation in order to improve understanding of response to established treatments end identify new therapeutic targets; 2) elucidate the mechanisms of action of novel anticancer agents end identify biochemical changes resulting in resistance to these agents; 3) evaluate potential genetic contributions to efficacy and toxicity of anticancer treatments; end 4) assess the toxicity end initial activity of selected treatments in early phase clinical trials, with an emphasis on correlative studies that assess pharmacokinetics, pharmacogenetics end biological effects of agents in tumor cells. Forty-five members from 17 departments end divisions contribute to this effort, with total funding of $23.3M ($11.9M peer-reviewed, with 60.3% from NCI and 89.3% from the NIH overall). Since the lest competitive renewal, the program has generated 724 publications, 19% end 57% reflecting intra- end inter-programmatic collaborations, respectively. Notable accomplishments include demonstration that 1) the temoxifen metabolite endoxifen, which bypasses an important metabolic block in some patients, has activity in preclinical studies end early phase clinical trials; 2) PARP inhibitors kill BRCA1/2-mutent cells through e process that involves activation of the nonhomologous end-joining pathway, yielding e unique responder/no responder hypothesis that is being tested clinically; end 3) FKBP51, MMSET end cereblon ere important determinants of response to various therapies. Leadership of the program is provided by Scott Keufmenn, MD, PhD, end Zhenkun Lou, PhD. The program makes extensive use of Shared Resources, especially the cell analysis, proteomics, pathology research, gene analysis, pharmacology end pharmacy facilities, as well as the Clinical Research Office. Future goals of the program include the establishment of e focus on oncogene-induced metabolic changes as therapeutic targets in cancer, growth of a nascent screening/drug discovery effort, end encouragement of additional genomically guided trials to follow recently opened studies.

View original record on NIH RePORTER →