Personal profile
Personal profile
Dr. Richard Hurwitz received his M.D. degree from Albany Medical College. After graduating from medical school, Dr. Hurwitz completed his residency and fellowship at the University of Minnesota. He studies the potential use of gene therapy for the treatment of ocular diseases.
He has developed a treatment for retinoblastoma using suicide gene therapy that is currently in clinical trials. To further refine this therapeutic option, Dr. Hurwitz is studying the cellular origin of retinoblastoma and the differences between invasive and non-invasive forms of the disease.
In addition, he is also using in vivo models of retinitis pigmentosa and macular degeneration to develop gene therapy treatments for retinal degenerative diseases. The mechanism of adenoviral-mediated transgene expression in the ocular environment is being explored with the goals of identifying molecular targets to modulate adenoviral-mediated gene therapy for both retinoblastoma and retinal degenerative diseases.
Research interests
The Hurwitz laboratory studies the use of gene therapy in the treatment of ocular disease. Retinoblastoma is the most common malignant intraocular tumor of children and is caused by mutations in the retinoblastoma gene.
Using a model of this disease, they have shown that suicide gene therapy using an adenoviral vector to deliver the herpes thymidine kinase gene followed by treatment with ganciclovir can ablate tumors. Based on these studies, an FDA- and RAC-approved clinical trial was opened to investigate the use of this therapy for children with retinoblastoma.
Free-text keywords
- Hematology
- Retinoblastoma
- Gene therapy
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Inhibitors of metalloprotease, γ-sectretase, protein kinase C and Rho kinase inhibit wild-type adenoviral replication
Liu, A., Ildefonso, C. J., Bond, W. S., Hurwitz, M. Y. & Hurwitz, R. L., Jul 2020, In: PLoS ONE. 15, 7, e0236175.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
Novel dose escalation to predict treatment with hydroxyurea (NDEPTH): A randomized controlled trial of a dose-prediction equation to determine maximum tolerated dose of hydroxyurea in pediatric sickle cell disease
George, A., Dinu, B., Estrada, N., Minard, C. G., Hurwitz, R., Mahoney, D. H., Yates, A. M., Vaughan, M., Carmouche, A., Airewele, G., Kirk, S. E., Fasipe, T., Uwaezuoke, P. & Ware, R. E., Sep 1 2020, In: American Journal of Hematology. 95, 9, p. E242-E244Research output: Contribution to journal › Letter › peer-review
4 Link opens in a new tab Scopus citations -
Versican G1 domain enhances adenoviral-mediated transgene expression and can be modulated by inhibitors of the Janus kinase (JAK)/STAT and Src family kinase pathways
Akinfenwa, P. Y., Bond, W. S., Ildefonso, C. J., Hurwitz, M. Y. & Hurwitz, R., Sep 1 2017, In: Journal of Biological Chemistry. 292, 35, p. 14381-14390 10 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Link opens in a new tab Scopus citations -
Intravenous injection of oncolytic picornavirus SVV-001 prolongs animal survival in a panel of primary tumor-based orthotopic xenograft mouse models of pediatric glioma
Liu, Z., Zhao, X., Mao, H., Baxter, P. A., Huang, Y., Yu, L., Wadhwa, L., Su, J. M., Adesina, A., Perlaky, L., Hurwitz, M., Idamakanti, N., Police, S. R., Hallenbeck, P. L., Hurwitz, R. L., Lau, C. C., Chintagumpala, M., Blaney, S. M. & Li, X. N., Sep 2013, In: Neuro-oncology. 15, 9, p. 1173-1185 13 p.Research output: Contribution to journal › Article › peer-review
77 Link opens in a new tab Scopus citations -
Tumorspheres but Not Adherent Cells Derived from Retinoblastoma Tumors Are of Malignant Origin
Bond, W. S., Akinfenwa, P. Y., Perlaky, L., Hurwitz, M. Y., Hurwitz, R. & Chévez-Barrios, P., Jun 24 2013, In: PLoS ONE. 8, 6, e63519.Research output: Contribution to journal › Article › peer-review
20 Link opens in a new tab Scopus citations