Rajesh Chopra
Team Leader
Translational Cancer Discovety
The Institute Of Cancer Research
United Kingdom
Biography
Professor Raj Chopra trained in Medicine at University College London. He then completed his training in general medicine at major teaching hospitals in London, gaining Membership of the Royal College of Physicians. He undertook a PhD in cell signaling and growth receptors followed by a postdoctoral fellowship at the Walter and Eliza Hall Institute of Medical Research in Melbourne, Australia. Subsequently, he set up his own research group in Stem Cell and Leukemia Biology at the Paterson Institute of Cancer Research in Manchester, UK. He was also appointed Director of Hematological Oncology, leading one of the largest Bone Marrow Transplant and Leukemia Programs in Europe at the Christie Hospital in Manchester. From 2004–09, he was part of the leadership team for the largest Oncology group in AstraZeneca and established Translational Medicine for AstraZeneca in Boston, Massachusetts, US. He was involved in taking six small molecules and two antibodies from discovery into clinical trials. From 2009–16, he was a leader within the Executive R&D Team and Corporate Vice President of Translational and Early Drug Development at Celgene Corporation, Summit, New Jersey, US, where he led a team of over 100 scientists in San Diego, San Francisco and Seville, and a team of clinicians involved in taking agents from discovery to proof-of-concept clinical trials in oncology and immune/inflammatory disease, as well as stem cell therapies.
Research Interest
These teams were responsible for taking nine small molecule and one antibody projects into early clinical trials in healthy volunteers and patients. Professor Chopra was also involved in the New Drug Applications for pomalidomide (a second generation IMiD agent) and a premilast (a PDE4 inhibitor). Both drugs were approved in 2013 and 2014 respectively. He also led the team that worked the mechanism of action of thalidomide and its analogues leading to the discovery of Aiolos, Ikaros and Caosin kinase1a as neo-substrates of the CUL4CRBN E-3 ligase family. He has been a member of the Medical Research Council (MRC) Molecular and Cell Biology Board and the MRC Stem Cell Committee. He has extensive experience of successful partnering with biotech. In addition, he has been a Non-Executive Director for e-Therapeutics (Oxford, UK) and has been on the Board of Agios (Boston, Massachusetts, US). In January 2016, he moved back to the UK to take up the position as Director of the Cancer Research UK Cancer Therapeutics Unit and Head of the Division of Cancer Therapeutics. He is currently a member of the Cancer Research UK Drug Discovery Committee and of the Scientific Board of the California Institute of Regenerative Medicine (CIRM).
Publications
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van der Velden, J.L., Ye, Y., Nolin, J.D., Hoffman, S.M., Chapman, D.G., Lahue, K.G., Abdalla, S., Chen, P., Liu, Y., Bennett, B., et al. (2016). JNK inhibition reduces lung remodeling and pulmonary fibrotic systemic markers. Clinical and translational medicine, Vol.5(1), p. 36
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Wei, W., Shin, Y.S., Xue, M., Matsutani, T., Masui, K., Yang, H., Ikegami, S., Gu, Y., Herrmann, K., Johnson, D., et al. (2016). Single-Cell Phosphoproteomics Resolves Adaptive Signaling Dynamics and Informs Targeted Combination Therapy in Glioblastoma. Cancer cell, Vol.29(4), pp. 563-573.
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Rychak, E., Mendy, D., Shi, T., Ning, Y., Leisten, J., Lu, L., Miller, K., Narla, R.K., Orlowski, R.Z., Raymon, H.K., et al. (2016). Pomalidomide in combination with dexamethasone results in synergistic anti-tumour responses in pre-clinical models of lenalidomide-resistant multiple myeloma. British journal of haematology, Vol.172(6), pp. 889-901.
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Collins, I., wang, H., caldwell, J. & chopra, R. (2017). Chemical approaches to targeted protein degradation through modulation of the ubiquitin proteasome pathway. Biochemical journal, Vol.474(7), pp. 1127-1147.
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Ear, J., Huang, H., Wilson, T., Tehrani, Z., Lindgren, A., Sung, V., Laadem, A., Daniel, T.O., Chopra, R. & Lin, S., et al. (2015). RAP-011 improves erythropoiesis in zebrafish model of Diamond-Blackfan anemia through antagonizing lefty1. Blood, Vol.126(7), pp. 880-890.