John McDonald - Arnoldsville GA, US Nathan John Bowen - Atlanta GA, US LiJuan Wang - Smyrna GA, US
Assignee:
Georgia Tech Research Corporation - Atlanta GA
International Classification:
A61K 31/7105 A61K 9/51 A61K 45/06
US Classification:
424497, 514 44 A
Abstract:
The present invention provides a method of treating an ovarian cancer, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to treat the ovarian cancer. Also provided are methods of preventing metastasis of an ovarian cancer, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to prevent metastasis. Further provided are methods of sensitizing an ovarian cancer to a cytotoxic therapy, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to sensitize the ovarian cancer to the cytotoxic therapy. The invention also contemplates methods of reducing epithelial-to-mesenchymal transition (EMT) in an ovarian cancer or cancer cell as well as methods of inducing mesenchymal-to-epithelial transition (MET).
Metabolomics-Based Identification Of Disease-Causing Agents
Jeffrey Skolnick - Roswell GA, US Adrian K. Arakaki - Marietta GA, US Susana Noemi Do Brito Afonso - Santa Fe, AR John McDonald - Arnoldsville GA, US Roman Mezencev - Atlanta GA, US Nathan Bowen - Atlanta GA, US
Assignee:
GEORGIA TECH RESEARCH CORPORATION - Atlanta GA
International Classification:
G06F 19/00 A61K 38/14
US Classification:
702 20, 514 209
Abstract:
A method, computer-readable medium, and system for identifying one or more metabolites associated with a disease, comprising: comparing gene expression data from diseased cells to gene expression data from control cells in order to deduce genes that are differentially-regulated in the diseased cells relative to the control cells; based on enzyme function and pathway data for all human metabolites that utilize the genes that are differentially-regulated in the disease cells, identifying one or more metabolites whose intracellular levels are higher or lower in diseased cells than in control cells, and thereby associating the one or more metabolites with the disease.
- Atlanta GA, US Nathan John Bowen - Atlanta GA, US
International Classification:
C07K 14/47 C12N 15/11 C12N 9/22 C12N 15/85
Abstract:
Human cell lines mutant for ZIC2 with altered cellular phenotype are disclosed, including HEK 293T, LN prostate cancer, and PC-3 cell lines. Method of making the human cell lines mutant for ZIC2 using gene editing tools such as CRISPR/Cas9 is also disclosed herein. Phenotypic characterization of the clonal mutant lines revealed altered cellular phenotypes relative to the parental lines. For example, ZIC2 protein expression is lost or lowered in these cell lines by western blot analyses. The human cell lines mutant for ZIC2 have various utilities including cancer diagnosis and prognosis.
Mir-200 Family Induces Mesenchymal-To-Epithelial Transition (Met) In Ovarian Cancer Cells
The present invention provides a method of treating an ovarian cancer, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to treat the ovarian cancer. Also provided are methods of preventing metastasis of an ovarian cancer, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to prevent metastasis. Further provided are methods of sensitizing an ovarian cancer to a cytotoxic therapy, the method comprising delivering one or more miR-200 family members to a mammalian subject in need thereof in an amount effective to sensitize the ovarian cancer to the cytotoxic therapy. The invention also contemplates methods of reducing epithelial-to-mesenchymal transition (EMT) in an ovarian cancer or cancer cell as well as methods of inducing mesenchymal-to-epithelial transition (MET).
Metabolomics-Based Identification Of Disease-Causing Agents
A method, computer-readable medium, and system for identifying one or more metabolites associated with a disease, comprising: comparing gene expression data from diseased cells to gene expression data from control cells in order to deduce genes that are differentially-regulated in the diseased cells relative to the control cells; based on enzyme function and pathway data for all human metabolites that utilize the genes that are differentially-regulated in the disease cells, identifying one or more metabolites whose intracellular levels are higher or lower in diseased cells than in control cells, and thereby associating the one or more metabolites with the disease.
Handelin Law, LLC - Carson City, Nevada since Aug 2013
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Education:
University of Nevada 2009 - 2012
Bachelor's degree, Criminal Justice; Pre-Law
Arbor View High School 2004 - 2008
High School Diploma
Laboratory of Cancer Development and Evolution @ CCRTD at Clark Atlanta University
Location:
Greater Atlanta Area
Industry:
Higher Education
Work:
Clark Atlanta University since Jan 2011
Laboratory of Cancer Development and Evolution @ CCRTD
Georgia Institute of Technology 2004 - 2010
SENIOR RESEARCH SCIENTIST
University of Georgia 2002 - 2004
SENIOR RESEARCH SCIENTIST
National Institutes of Health 2000 - 2002
POSTDOCTORAL FELLOW
USDA Plant Genetic Resources Conservation Unit Jan 1993 - Jan 1994
RESEARCH COORDINATOR
Education:
The University of Georgia 1994 - 2000
PHD, Genetics
Georgia Institute of Technology 1990 - 1992
BACHELOR OF SCIENCE, Applied Biology
Gordon College (GA) 1988 - 1990
ASSOCIATE OF SCIENCE, Chemistry
Skills:
Genomics Cell Biology Translational Research Molecular Evolution Cancer Cancer Research Molecular Biology PCR Computational Biology Sequencing Bioinformatics Higher Education Genetics Transposable Elements
Interests:
Prostate and Ovarian Cancer Basic and Translational Research
Manager, Application Support At Mckesson Corporation
Carbondale Elementary School Carbondale CO 1987-1991, Nisley Elementary School Grand Junction CO 1991-1993, Bookcliff Middle School Grand Junction CO 1993-1996, Howe High School Howe OK 1999-2001