Jonathan E. McDunn - University City MO, US William G. Hawkins - Olivette MO, US Robert H. Mach - Eureka MO, US Richard A. Hotchkiss - Chesterfield MO, US
Pharmaceutical compounds, pharmaceutical compositions and methods of treatment are disclosed, wherein a compound comprises a targeting moiety which, in free form, binds a cell receptor with a dissociation constant Kof less than about 10M, and a pharmaceutically active moiety, wherein the targeting moiety is other than an oligopeptide, a polypeptide, a peptidomimetic, a protein or a protein domain, and wherein the targeting moiety and the pharmaceutically active moiety are covalently attached. In some aspects, the targeting moiety binds a sigma-2 receptor with high affinity and high specificity, and the pharmaceutically active moiety is a pro-apoptotic peptide moiety. Methods of cancer treatment are disclosed comprising administering a disclosed pharmaceutical compound to a subject in need of thereof. The treatments selectively induce apoptosis in cancer cells. These methods can further comprise co-administration of radiation therapy and/or an additional chemotherapeutic agent.
Membrane-Permeant Peptide Complexes For Treatment Of Sepsis
Richard Hotchkiss - Chesterfield MO, US David Piwnica-Worms - Ladue MO, US Jonathan McDunn - University City MO, US
International Classification:
A61K 48/00 C07K 14/475
US Classification:
514012000, 514044000, 530352000
Abstract:
Methods and compositions for treating sepsis using cell membrane-permeant peptide conjugate covalent compounds having target cell specificity are provided.
Membrane-Permeant Peptide Complexes For Treatment Of Sepsis
Richard Hotchkiss - Chesterfield MO, US David Piwnica-Worms - Ladue MO, US Jonathan McDunn - University City MO, US
International Classification:
A61K 39/00
US Classification:
424185100
Abstract:
Methods and compositions for treating sepsis and diseases and conditions involving cellular apoptosis using cell membrane-permeant peptide conjugates of a cell membrane permeant peptide together with anti-apoptotic domains of the TCL1 protein are provided.
Richard Hotchkiss - Chesterfield MO, US Jonathan McDunn - University City MO, US David Piwnica-Worms - St. Louis MO, US Steven Schwulst - St. Louis MO, US
International Classification:
A61K 31/7105 A61P 31/04
US Classification:
514 44
Abstract:
Methods of treatment of sepsis are disclosed. These methods comprise administering to a subject a composition comprising at least one siRNA directed against at least one gene encoding a pro-apoptotic polypeptide. The pro-apoptotic polypeptide, in some aspects, can be other than Fas or caspase-8. In some embodiments, an siRNA can be directed against a pro-apoptotic component of the mitochondrial pathway, such as a pro-apoptotic bcl-2 protein. In some aspects, an siRNA can be directed against a BH3-only bcl-2 protein, while in other aspects, siRNAs can be directed against multi BH domain Bcl-2 family members such as bax and bak. In some embodiments, an siRNA can be directed against a death receptor pathway molecule such as FADD. In various configurations, a composition can also comprise a cationic lipid such as DOTAP, or nanoparticles comprising a cyclodextrin-containing polycation and a polymer such as a poly(ethylene glycol).
Membrane-Permeant Peptide Complexes For Treatment Of Sepsis
Richard Hotchkiss - Chesterfield MO, US David Piwnica-Worms - Ladue MO, US Jonathan McDunn - University City MO, US
Assignee:
WASHINGTON UNIVERSITY - St. Louis MO
International Classification:
C07K 14/435
US Classification:
530350
Abstract:
Methods and compositions for treating sepsis and diseases and conditions involving cellular apoptosis using cell membrane-permeant peptide conjugates of a cell membrane permeant peptide together with anti-apoptotic domains of the TCL1 protein are provided.
Biomarkers For Prostate Cancer And Methods Using The Same
Jeffrey R. Shuster - Chapel Hill NC, US Matthew W. Mitchell - Durham NC, US Jonathan E. McDunn - Cary NC, US Bruce Neri - Cary NC, US
Assignee:
METABOLON, INC. - Durham NC
International Classification:
G01N 33/574 A61K 31/7072 A61K 31/685
US Classification:
514 51, 436501, 435 792, 435 71, 514114
Abstract:
Biomarkers (and suites of biomarkers) relating to prostate cancer are provided, as well as methods for using such biomarkers (ans suites thereof), including early prediction of prostate cancer, disease grading, target identification/validation, and monitoring of drug efficacy.
Methods of preparing nitric oxide-releasing silica particles are provided, including the steps of functionalizing a silica particle with a linker moiety; and reacting a functional group on a nitric oxide storage/release compound with the linker moiety to attach the nitric oxide storage/release compound to the silica particle via the linker moiety. The disclosure also provides certain nitric oxide-releasing silica particles and precursors thereof, as well as compositions containing such particles.
2011 to 2000 Adjunct Associate Professor of Biomedical EngineeringMetabolon, Inc
2011 to 2000 Associate Director, Diagnostic Development Project ManagementMetabolon, Inc. Durham, NC 2009 to 2010 Senior Study DirectorWashington University School of Medicine St. Louis, MO 2006 to 2009 Research Assistant Professor of AnesthesiologyWashington University Office of Technology Management
2003 to 2006 Postdoctoral Research FellowIncyte Genomics Palo Alto, CA 1996 to 1999 Senior Research AssociateCombion, Inc Pasadena, CA 1996 to 1996 Research Scientist
Education:
The Scripps Research Institute 2003 Ph.D. in BiologyCalifornia Institute of Technology 1996 B.S. in Chemistry