This renewal application involves synthesis, computer modeling, mechanistic/mode of action, biological and medicinal studies focused on compounds of demonstrated or potential importance in cancer research and chemotherapy. A special emphasis is placed on compounds possessing novel structures, novel or unique modes of action, and significant clinical potential. It is the objective of this program to develop fundamentally new methods and strategies for the synthesis and modification of such compounds, to elucidate the structural basis for their mode of action, and to exploit these new findings in the rational design of novel cancer chemotherapeutic agents or compounds of interest in cancer research and chemotherapy. Section D.1 describes a continuation of studies on the computer assisted design, synthesis, biological evaluation, and pre-clinical advancement of a new and therapeutically promising family of bryostatin analogues that exhibit superior in vitro potency relative to bryostatin, a promising chemotherapeutic agent now in clinical trials. Section D.2 describes studies on the isolation, characterization, derivatization, semi-synthesis, mode of action, and biological evaluation of the apoptolidins, a promising new family of novel therapeutic leads, that exhibit exceptional and therapeutically desirable selectivity in inducing apoptosis in oncogenically transformed cells relative to normal cells. Section D.3 describes studies on the use of new catalyzed reactions to incorporate pharmacophoric subunits into new scaffolds to generate novel cancer therapeutic leads based on the modulation of kinase activity. Section D.4 describes studies on molecular transporters designed to enable or enhance uptake into cells and tissues of drug candidates or drugs that do not enter cells or do so only poorly. These studies will focus on mechanism of uptake with an emphasis on single molecule studies and the synthesis and evaluation of new transporters including their ability to enter cells and tissue (transgenic mice) and release drugs or probes at therapeutic levels.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
3R37CA031845-29S1
Application #
7916866
Study Section
Synthetic and Biological Chemistry B Study Section (SBCB)
Program Officer
Ogunbiyi, Peter
Project Start
1981-07-01
Project End
2011-05-31
Budget Start
2009-09-01
Budget End
2010-05-31
Support Year
29
Fiscal Year
2009
Total Cost
$67,848
Indirect Cost
Name
Stanford University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
McKinlay, Colin J; Benner, Nancy L; Haabeth, Ole A et al. (2018) Enhanced mRNA delivery into lymphocytes enabled by lipid-varied libraries of charge-altering releasable transporters. Proc Natl Acad Sci U S A 115:E5859-E5866
Fernandes-Cunha, Gabriella M; McKinlay, Colin J; Vargas, Jessica R et al. (2018) Delivery of Inorganic Polyphosphate into Cells Using Amphipathic Oligocarbonate Transporters. ACS Cent Sci 4:1394-1402
Haabeth, Ole A W; Blake, Timothy R; McKinlay, Colin J et al. (2018) mRNA vaccination with charge-altering releasable transporters elicits human T cell responses and cures established tumors in mice. Proc Natl Acad Sci U S A 115:E9153-E9161
Khan, Tapan K; Wender, Paul A; Alkon, Daniel L (2018) Bryostatin and its synthetic analog, picolog rescue dermal fibroblasts from prolonged stress and contribute to survival and rejuvenation of human skin equivalents. J Cell Physiol 233:1523-1534
Marsden, Matthew D; Wu, Xiaomeng; Navab, Sara M et al. (2018) Characterization of designed, synthetically accessible bryostatin analog HIV latency reversing agents. Virology 520:83-93
Ryckbosch, Steven M; Wender, Paul A; Pande, Vijay S (2017) Molecular dynamics simulations reveal ligand-controlled positioning of a peripheral protein complex in membranes. Nat Commun 8:6
McKinlay, Colin J; Vargas, Jessica R; Blake, Timothy R et al. (2017) Charge-altering releasable transporters (CARTs) for the delivery and release of mRNA in living animals. Proc Natl Acad Sci U S A 114:E448-E456
Wender, Paul A; Ebner, Christian; Fennell, Brandon D et al. (2017) Ynol Ethers as Ketene Equivalents in Rhodium-Catalyzed Intermolecular [5 + 2] Cycloaddition Reactions. Org Lett 19:5810-5813
Staveness, Daryl; Abdelnabi, Rana; Near, Katherine E et al. (2016) Inhibition of Chikungunya Virus-Induced Cell Death by Salicylate-Derived Bryostatin Analogues Provides Additional Evidence for a PKC-Independent Pathway. J Nat Prod 79:680-4
Pavlovic, Igor; Thakor, Divyeshsinh T; Vargas, Jessica R et al. (2016) Cellular delivery and photochemical release of a caged inositol-pyrophosphate induces PH-domain translocation in cellulo. Nat Commun 7:10622

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