Lee Rubin | Director of Translational Medicine
Harvard Stem Cell Institute

Lee Rubin, Director of Translational Medicine, Harvard Stem Cell Institute

Dr. Rubin received his Ph.D. in Neuroscience from The Rockefeller University and completed postdoctoral fellowships in Pharmacology from Harvard Medical School and in Neurobiology from Stanford University School of Medicine. He has worked both in academia and in industry. Notably, at Athena Neurosciences (now Elan Pharmaceuticals), he initiated a project that lead to the discovery of an antibody that blocks lymphocyte trafficking across the BBB. This work culminated in the development of an anti-integrin antibody, now known as Tysabri, which has been approved for treatment of multiple sclerosis. Subsequently, he became Chief Scientific Officer of Ontogeny, Inc (now Curis, Inc), a biotechnology company in Cambridge, MA, founded by Dr. Douglas Melton. Dr. Rubin's work there centered on the hedgehog (Hh) pathway and its involvement in cancer and neurodegenerative disease. Potent small molecule Hh antagonists were identified by his group and partnered with Genentech for clinical development. Numerous clinical trials to test the effects of hedgehog antagonists on different types of solid tumors are currently underway. Dr. Rubin is currently Professor of Stem Cell and Regenerative Biology at Harvard University and Director of Translational Medicine at the Harvard Stem Cell Institute. Much of his effort is devoted to identifying therapeutics for orphan neural disorders such as Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis, using new kinds of stem cell-based screens. His lab also explores different chemical biology approaches for manipulating cell fate. Some of this work has been published recently in Cell, Cell Stem Cell, Nature Chemical Biology and Science.

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Appearances at this years' conference:

DAY ONE: Stream B: Stem Cells for Drug Discovery


@ 15.00
Drug discovery using disease-specific iPS models

  • What are the challenges of generating iPS cells using a diseased model?
  • What are the benefits promised?
  • Should cell types not targeted by drugs be tested for side effects?
  • Could this be the ultimate in personalised medicine?

  • › Lee Rubin, Director of Translational Medicine, Harvard Stem Cell Institute
@ 17.35
Panel discussion: understanding the appropriate stem cell type as a platform for your drug discovery protocol

  • Comparing iPS cells, hES cells, and cancer stem cells as effective drug discovery tools
  • What are the benefits of using these cell types?
  • How are stem cells incorporated into existing paradigms of drug development?
  • What is the potential for stem cell-based drug discovery in personalised medicine?

  • › Lee Rubin, Director of Translational Medicine, Harvard Stem Cell Institute
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