In the last decade there has been an exponential growth in nanotechnology research in cancer demonstrating that nanotechnology could provide unique and otherwise unattainable solutions to cancer management including very early cancer detection, accurate molecular specific diagnosis and treatment that diminishes side effects. However, achieving this promise is extremely challenging because it requires overcoming multiple constraints imposed by translational barriers in clinical applications of nanomaterials that is multiplied by complexity of cancer biology. Currently, there is a growing gap between new discoveries coming at a fast pace from academic labs and their translation into clinic. Therefore, there is an urgent need in addressing this gap in cancer nanotechnology translational pipeline. To this end, we have designed a novel training program to educate future leaders in the broad field of nanotechnology with specific interests in cancer-related applications, who are keenly aware of the needs and demands of clinical environment as well as of major challenges of translational research. We believe that the only way to train cancer translation minded Ph.D. researchers is to insert them into the environment of an outstanding cancer center. Therefore, our program is based on a close collaboration between The University of Texas MD Anderson Cancer Center and Rice University. As part of our program, we have developed a comprehensive plan for recruiting trainees from underrepresented minority groups that are historically underrepresented in health-related research, including women, minority individuals, and individuals with disabilities. Our training program includes multidisciplinary mentorship of translational research projects combined with multidisciplinary, hands-on coursework and seminar experiences. All trainees will work with at least two program faculty mentors (one from Rice and one from MD Anderson) to define and carry out an independent research problem. Didactic coursework will prepare them to contribute to research projects that directly address barriers to translation of nanotechnology-based approaches and to develop the skills needed to define and lead such projects. Incoming trainees will participate in a unique 2-week-long boot camp in Cancer Management and Nanotechnology that provides an overview of current opportunities and barriers in the field. Trainees will develop foundational background in the field by taking four courses related to translational cancer or nanotechnology topics. Trainees will gain an appreciation for federal resources to assist in cancer nanotechnology research by taking a trip to the NCI Nanotechnology Characterization Lab. Finally, trainees will gain important lab management skills by participating in a short hands-on course providing an introduction to laboratory and project management. At the end of the program, fellows will have a deep understanding of translational research in cancer nanotechnology, with the most important component being the demonstrated ability to carry out independent translational research in this challenging multidisciplinary field.
Currently, there is a growing gap between new discoveries in cancer nanotechnology and their translation into clinic. To address this problem, we have designed a novel training program to prepare Ph.D. scientists who will transfer the many promises of cancer nanotechnology into clinical reality of the future.
| Evans, Emily Reiser; Bugga, Pallavi; Asthana, Vishwaratn et al. (2018) Metallic Nanoparticles for Cancer Immunotherapy. Mater Today (Kidlington) 21:673-685 |
| Thomas, Jonathan G; Parker Kerrigan, Brittany C; Hossain, Anwar et al. (2018) Ionizing radiation augments glioma tropism of mesenchymal stem cells. J Neurosurg 128:287-295 |
| Samson, Edward B; Tsao, David S; Zimak, Jan et al. (2017) The coordinating role of IQGAP1 in the regulation of local, endosome-specific actin networks. Biol Open 6:785-799 |
| Parker Kerrigan, Brittany C; Shimizu, Yuzaburo; Andreeff, Michael et al. (2017) Mesenchymal stromal cells for the delivery of oncolytic viruses in gliomas. Cytotherapy 19:445-457 |
| Srinivasan, Visish M; Ferguson, Sherise D; Lee, Sungho et al. (2017) Tumor Vaccines for Malignant Gliomas. Neurotherapeutics 14:345-357 |
| Yaghi, Nasser K; Wei, Jun; Hashimoto, Yuuri et al. (2017) Immune modulatory nanoparticle therapeutics for intracerebral glioma. Neuro Oncol 19:372-382 |
| Figueroa, Elizabeth; Bugga, Pallavi; Asthana, Vishwaratn et al. (2017) A mechanistic investigation exploring the differential transfection efficiencies between the easy-to-transfect SK-BR3 and difficult-to-transfect CT26 cell lines. J Nanobiotechnology 15:36 |
| Poulose, Aby Cheruvathoor; Veeranarayanan, Srivani; Mohamed, M Sheikh et al. (2016) Multifunctional Cu2-xTe Nanocubes Mediated Combination Therapy for Multi-Drug Resistant MDA MB 453. Sci Rep 6:35961 |
| Chen, Allen L; Jackson, Meredith A; Lin, Adam Y et al. (2016) Changes in Optical Properties of Plasmonic Nanoparticles in Cellular Environments are Modulated by Nanoparticle PEGylation and Serum Conditions. Nanoscale Res Lett 11:303 |
| Wolfe, Adam R; Trenton, Nicholaus J; Debeb, Bisrat G et al. (2016) Mesenchymal stem cells and macrophages interact through IL-6 to promote inflammatory breast cancer in pre-clinical models. Oncotarget 7:82482-82492 |
