Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States
Santosh Hariharan
Biological Sciences Platform, Sunnybrook Research Institute, University of Toronto, Ontario, Canada; Department of Medical Biophysics, University of Toronto, Ontario, Canada
Jarkko Ylanko
Biological Sciences Platform, Sunnybrook Research Institute, University of Toronto, Ontario, Canada; Department of Medical Biophysics, University of Toronto, Ontario, Canada
Luis Orozco
Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States
Fu-Yue Zeng
Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States
Ian Pass
Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States
Fernando Ugarte
Department of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, United States; Institute for the Biology of Stem Cells, University of California, Santa Cruz, Santa Cruz, United States
E Camilla Forsberg
Department of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, United States; Institute for the Biology of Stem Cells, University of California, Santa Cruz, Santa Cruz, United States
Chun-Teng Huang
Sanford Burnham Prebys Medical Discovery Institute, La Jolla, United States
Biological Sciences Platform, Sunnybrook Research Institute, University of Toronto, Ontario, Canada; Department of Medical Biophysics, University of Toronto, Ontario, Canada; Department of Biochemistry, University of Toronto, Ontario, Canada
High-content phenotypic screening has become the approach of choice for drug discovery due to its ability to extract drug-specific multi-layered data. In the field of epigenetics, such screening methods have suffered from a lack of tools sensitive to selective epigenetic perturbations. Here we describe a novel approach, Microscopic Imaging of Epigenetic Landscapes (MIEL), which captures the nuclear staining patterns of epigenetic marks and employs machine learning to accurately distinguish between such patterns. We validated the MIEL platform across multiple cells lines and using dose-response curves, to insure the fidelity and robustness of this approach for high content high throughput drug discovery. Focusing on noncytotoxic glioblastoma treatments, we demonstrated that MIEL can identify and classify epigenetically active drugs. Furthermore, we show MIEL was able to accurately rank candidate drugs by their ability to produce desired epigenetic alterations consistent with increased sensitivity to chemotherapeutic agents or with induction of glioblastoma differentiation.