Ruth A. Gjerset - San Diego CA, US Keya Bandyopadhyay - San Diego CA, US
Assignee:
RG Biopharma LLC - San Diego CA
International Classification:
G01N 33/574 C12Q 1/00 A01N 43/42
US Classification:
435 723, 435 4, 514283
Abstract:
Disclosed herein are methods and compositions for determining the sensitivity or enhancing the sensitivity of cells to the effects of topoisomerase I inhibitors. Also disclosed are methods and compositions for inducing cell death, apoptosis and/or growth arrest which may be used for tumor suppression.
Enhancing The Sensitivity Of Tumor Cells To Therapies
Robert Sobol - Rancho Santa Fe CA, US Ruth Gjerset - San Diego CA, US
International Classification:
A61K048/00
US Classification:
514/044000
Abstract:
A method for enhancing the effect of a cancer therapy by introducing wild-type therapy-sensitizing gene activity into tumor cells having mutant therapy-sensitizing gene activity and subjecting the tumor cells to a cancer therapy such as chemotherapy, radiotherapy, biological therapy including immunotherapy, cryotherapy and hyperthermia.
Enhancing The Sensitivity Of Tumor Cells To Therapies
Robert Sobol - Rancho Santa Fe CA, US Ruth Gjerset - San Diego CA, US
International Classification:
A61K048/00
US Classification:
514/044000
Abstract:
A method for enhancing the effect of a cancer therapy by introducing wild-type therapy-sensitizing gene activity into tumor cells having mutant therapy-sensitizing gene activity and subjecting the tumor cells to a cancer therapy such as chemotherapy, radiotherapy, biological therapy including immunotherapy, cryotherapy and hyperthermia.
Enhancing The Sensitivity Of Tumor Cells To Therapies
Robert Sobol - Rancho Santa Fe CA, US Ruth Gjerset - San Diego CA, US
International Classification:
A61K048/00
US Classification:
514/044000
Abstract:
A method for enhancing the effect of a cancer therapy by introducing wild-type therapy-sensitizing gene activity into tumor cells having mutant therapy-sensitizing gene activity and subjecting the tumor cells to a cancer therapy such as chemotherapy, radiotherapy, biological therapy including immunotherapy, cryotherapy and hyperthermia.
Tumor Suppression Through Bicistronic Co-Expression Of P53 And P14Arf
Ruth Gjerset - San Diego CA, US Yinghui Huang - San Diego CA, US Neshat Saadatmandi - San Diego CA, US
International Classification:
A61K048/00 A61K009/127 C12N015/86
US Classification:
514044000, 424450000, 435320100, 435456000
Abstract:
A bicistronic construct of pand pARF, vectors and other delivery vehicles which include the bicistronic construct, and methods of treating cancer using the vectors and bicistronic construct.
Down-Regulation Of Dna Repair To Enhance Sensitivity To P53-Mediated Suppression
The present invention details methods for the treatment of cancer. In particular, it concerns the induction of apoptosis in cancer cells following treatment with inhibitors of DNA repair in combination with p53 gene therapy. Treatment of glioblastoma and breast tumor cells with inhibitors of DNA repair induced growth suppression that was a result of p53-mediated apoptosis. Thus it appears that inhibitors of DNA repair in combination with p53 gene therapy is involved in restoration of p53-mediated apoptosis.
Methods And Compositions For Topoisomerase I Modulated Tumor Suppression
Disclosed herein are methods and compositions for enhancing the sensitivity of cells to the effects of topoisomerase I inhibitors. Also disclosed are methods and compositions for inducing apoptosis and/or growth arrest which may be used for tumor suppression.
Down-Regulation Of Dna Repair To Enhance Sensitivity To P53-Mediated Apoptosis
The present invention details methods for the treatment of cancer. In particular it concerns the induction of apoptosis in cancer cells following treatment with inhibitors of DNA repair in combination with p53. Treatment of glioblastoma and breast tumor cells with inhibitors of DNA repair induced growth suppression that was a result of p53-mediated apoptosis. Thus it appears that inhibitors of DNA repair in combination with p53 is involved in restoration of p53-mediated apoptosis.
Torrey Pines Institute For Molecular Studies Mar 2009 - Jun 2014
Member and Head of Cancer Cell Biology
Rg Biopharma Mar 2009 - Jun 2014
Chief Executive Officer
Sidney Kimmel Cancer Center Aug 1991 - Mar 2009
Associate Professor
Education:
Uc San Diego 1986 - 1990
University of California, San Francisco
Doctorates, Doctor of Philosophy, Biochemistry, Biophysics, Philosophy
Uc San Diego
Bachelors, Bachelor of Arts, Biology