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Cancer Chemical and Structural Biology

$54,277P30FY2022CANIH

Johns Hopkins University, Baltimore MD

Investigators

Linked publications, trials & patents

Trial NCT02989636Trial NCT02516670Trial NCT02491411Trial NCT02489357Trial NCT02029950Trial NCT01935947Trial NCT01870596Trial NCT01783171Trial NCT01757639Trial NCT01578109Trial NCT01349972Trial NCT01349959Trial NCT01330173Trial NCT01264432Trial NCT01207726Trial NCT01207687Trial NCT01139970Trial NCT01132573Trial NCT01061749Trial NCT00971737Trial NCT00963807Trial NCT00899951Trial NCT00899548Trial NCT00898482Trial NCT00897338Trial NCT00897273Trial NCT00847171Trial NCT00795002Trial NCT00727441Trial NCT00673569Trial NCT00670917Trial NCT00660348Trial NCT00641303Trial NCT00641147Trial NCT00631137Trial NCT00616967Trial NCT00602771Trial NCT00588991Trial NCT00566098Trial NCT00524017Trial NCT00499733Trial NCT00499486Trial NCT00493025Trial NCT00492921Trial NCT00489281Trial NCT00478062Trial NCT00478010Trial NCT00471653Trial NCT00470093Trial NCT00469820Trial NCT00445484Trial NCT00433472Trial NCT00425477Trial NCT00407966Trial NCT00401024Trial NCT00389610Trial NCT00387465Trial NCT00381550Trial NCT00373191Trial NCT00369681Trial NCT00368914Trial NCT00363649Trial NCT00361296Trial NCT00356928Trial NCT00354640Trial NCT00343447Trial NCT00336063Trial NCT00334542Trial NCT00324870Trial NCT00313560Trial NCT00311623Trial NCT00305760Trial NCT00303927Trial NCT00293410Trial NCT00293397Trial NCT00293280Trial NCT00290732Trial NCT00287989Trial NCT00287872Trial NCT00281970Trial NCT00281866Trial NCT00278200Trial NCT00278161Trial NCT00278109Trial NCT00276744Trial NCT00276601Trial NCT00276588Trial NCT00274768Trial NCT00265915Trial NCT00265837Trial NCT00262834Trial NCT00258206Trial NCT00258180Trial NCT00255775Trial NCT00255710Trial NCT00245115Trial NCT00244959Trial NCT00242996Trial NCT00238368Trial NCT00238277

Abstract

PROJECT SUMMARY/ABSTRACT The major goals of the Sidney Kimmel Comprehensive Cancer Center (SKCCC) Cancer Chemical and Structural Biology (CCSB) Program are to: 1) discover, validate and characterize novel molecular targets for prospective therapeutic agents against human cancers; 2) identify and optimize new small molecules with anticancer potential; and 3) provide tools for targeting and assessing therapeutic delivery. To achieve these goals, CCSB fosters significant interactivity among its 31 Program Members and other SKCCC Members. The program is composed of 31 Members (28 Full Members and three Associate Members) (Table 1), across twelve departments and four schools. Of the 31 members, 26 have cancer-relevant peer-reviewed funding. The program brings together cross-disciplinary expertise throughout the university, including the School of Medicine, the Whiting School of Engineering, the Bloomberg School of Public Health, and the Krieger School of Arts and Sciences. The total direct cancer-relevant peer-reviewed funding is $8.9 million (Data Table 2A), with $2.1 million from the National Cancer Institute. The success of CCSB is evidenced by a robust pipeline of over 19 novel lead compounds in various stages of preclinical (14) and clinical (five) development. The scholarship, including 355 publications, demonstrates broad interactions of which 46 (13%) were Intra- Programmatic, 162 (45.6%) were Inter-Programmatic and 244 (68.7%) were external collaborations. Activities for the next project period focus on three synergistic aims: Aim 1: To accelerate anticancer target discovery and validation. Aim 2: To develop novel small-molecule screening platforms, and identify and optimize novel compounds against cancer targets. Aim 3: To develop methods for monitoring, predicting and optimizing anticancer drug delivery and immunomodulation. Aim 1 uses discovery-driven approaches to identify and validate targets along with proof-of-principle experiments to assess merit and feasibility for translational approaches. These activities include molecular, structural and cell biology studies, coupled with biological and preclinical therapeutic studies, and pharmacokinetic analyses. Aim 2 is focused on developing new small-molecule libraries and screening both existing and novel chemical libraries against identified cancer targets. Aim 3 centers on developing new methods for small-molecule and nucleic acid delivery (prodrugs, encapsulation methods), and for antibody design and use (immunoengineering). CCSB efforts will provide new preclinical drug candidates, along with the biology of pertinent molecular targets. These will support clinical translation and development by investigators across all SKCCC Programs. CCSB deliverables will have a broad and powerful impact on translational and clinical research, expediting basic science discoveries to promote the development of new cancer therapeutics.

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