Improving drug discovery using image-based multiparametric analysis of the epigenetic landscape

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.

[1]  M. Guenther,et al.  Histone Deacetylase Is a Direct Target of Valproic Acid, a Potent Anticonvulsant, Mood Stabilizer, and Teratogen* , 2001, The Journal of Biological Chemistry.

[2]  Tariq Parvez,et al.  Present Trend in the Primary Treatment of Aggressive Malignant Glioma: Glioblastoma Multiforme , 2008, Technology in cancer research & treatment.

[3]  Stefan Prechtl,et al.  Quantification of Histone H3 Lys27 Trimethylation (H3K27me3) by High-Throughput Microscopy Enables Cellular Large-Scale Screening for Small-Molecule EZH2 Inhibitors , 2015, Journal of biomolecular screening.

[4]  Kun-Yong Kim,et al.  Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome , 2011, Proceedings of the National Academy of Sciences.

[5]  Anne E Carpenter,et al.  Multiplex Cytological Profiling Assay to Measure Diverse Cellular States , 2013, PloS one.

[6]  W. Figg,et al.  Using Epigenetic Therapy to Overcome Chemotherapy Resistance. , 2016, Anticancer research.

[7]  M. Sanson,et al.  Dose optimization of MK-8628 (OTX015), a small molecule inhibitor of bromodomain and extra-terminal (BET) proteins, in patients (pts) with recurrent glioblastoma (GB). , 2016 .

[8]  Ling-Zhi Wang,et al.  Targetable BET proteins- and E2F1-dependent transcriptional program maintains the malignancy of glioblastoma , 2018, Proceedings of the National Academy of Sciences.

[9]  D. Botstein,et al.  Gene expression profiling reveals molecularly and clinically distinct subtypes of glioblastoma multiforme. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[10]  Anton Simeonov,et al.  Cell-based assays to support the profiling of small molecules with histone methyltransferase and demethylase modulatory activity. , 2015, Drug discovery today. Technologies.

[11]  Marissa Friedman,et al.  Glioblastoma: Molecular Pathways, Stem Cells and Therapeutic Targets , 2015, Cancers.

[12]  Lit-Hsin Loo,et al.  An approach for extensibly profiling the molecular states of cellular subpopulations , 2009, Nature Methods.

[13]  Dario Strbenac,et al.  Combining BET and HDAC inhibitors synergistically induces apoptosis of melanoma and suppresses AKT and YAP signaling , 2015, Oncotarget.

[14]  G. Peterson,et al.  Valproate: a simple chemical with so much to offer , 2005, Journal of clinical pharmacy and therapeutics.

[15]  Allan H Friedman,et al.  Phase II trial of temozolomide plus o6-benzylguanine in adults with recurrent, temozolomide-resistant malignant glioma. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[16]  Alan Ashworth,et al.  PARP inhibitors: Synthetic lethality in the clinic , 2017, Science.

[17]  Allan H Friedman,et al.  Phase I trial of temozolomide plus O6-benzylguanine 5-day regimen with recurrent malignant glioma. , 2009, Neuro-oncology.

[18]  Alan J. Tackett,et al.  Identification of Small Molecule Inhibitors of Jumonji AT-rich Interactive Domain 1B (JARID1B) Histone Demethylase by a Sensitive High Throughput Screen* , 2013, The Journal of Biological Chemistry.

[19]  R. McLendon,et al.  Phase 1 trial of temozolomide plus irinotecan plus O6‐benzylguanine in adults with recurrent malignant glioma , 2009, Cancer.

[20]  Hee Jin Cho,et al.  FoxM1 Promotes Stemness and Radio-Resistance of Glioblastoma by Regulating the Master Stem Cell Regulator Sox2 , 2015, PloS one.

[21]  A. Stark,et al.  Transcriptional enhancers: from properties to genome-wide predictions , 2014, Nature Reviews Genetics.

[22]  Georg Karpel-Massler,et al.  BH3-mimetics and BET-inhibitors elicit enhanced lethality in malignant glioma , 2017, Oncotarget.

[23]  T. Mikkelsen,et al.  Genome-wide maps of chromatin state in pluripotent and lineage-committed cells , 2007, Nature.

[24]  Simon Kasif,et al.  Reconstructing and Reprogramming the Tumor-Propagating Potential of Glioblastoma Stem-like Cells , 2014, Cell.

[25]  Andrew E. Teschendorff,et al.  Glioblastoma Stem Cells Respond to Differentiation Cues but Fail to Undergo Commitment and Terminal Cell-Cycle Arrest , 2015, Stem cell reports.

[26]  Z. Herceg,et al.  The Promises and Challenges of Toxico-Epigenomics: Environmental Chemicals and Their Impacts on the Epigenome , 2020, Environmental health perspectives.

[27]  Yirong Wang,et al.  DNMT1 mediates chemosensitivity by reducing methylation of miRNA-20a promoter in glioma cells , 2015, Experimental & Molecular Medicine.

[28]  Aaron A. Cohen-Gadol,et al.  Glioblastoma stem cells (GSCs) epigenetic plasticity and interconversion between differentiated non-GSCs and GSCs , 2015, Genes & diseases.

[29]  Fred H. Gage,et al.  A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells , 2010, Cell.

[30]  Yonghong Shi,et al.  High-content screening identifies kinase inhibitors that overcome venetoclax resistance in activated CLL cells. , 2016, Blood.

[31]  Mark W. Dewhirst,et al.  Glioma stem cells promote radioresistance by preferential activation of the DNA damage response , 2006, Nature.

[32]  Claes Wahlestedt,et al.  BET bromodomain proteins are required for glioblastoma cell proliferation , 2014, Epigenetics.

[33]  K. V. von Wangenheim,et al.  Control of cell proliferation by progress in differentiation: clues to mechanisms of aging, cancer causation and therapy. , 1998, Journal of theoretical biology.

[34]  Stephan Saikali,et al.  Prognostic value of O6-methylguanine-DNA methyltransferase status in glioblastoma patients, assessed by five different methods , 2010, Journal of Neuro-Oncology.

[35]  Florian Heigwer,et al.  Machine learning and image-based profiling in drug discovery , 2018, Current opinion in systems biology.

[36]  Alan J Tackett,et al.  Disruption of BRD4 at H3K27Ac-enriched enhancer region correlates with decreased c-Myc expression in Merkel cell carcinoma , 2015, Epigenetics.

[37]  R. Mirimanoff,et al.  MGMT gene silencing and benefit from temozolomide in glioblastoma. , 2005, The New England journal of medicine.

[38]  L. Ouafik,et al.  OTX015 (MK‐8628), a novel BET inhibitor, displays in vitro and in vivo antitumor effects alone and in combination with conventional therapies in glioblastoma models , 2016, International journal of cancer.

[39]  S. Rees,et al.  Principles of early drug discovery , 2011, British journal of pharmacology.

[40]  K. V. von Wangenheim,et al.  A mechanism of intracellular timing and its cooperation with extracellular signals in controlling cell proliferation and differentiation, an amended hypothesis. , 2001, Journal of theoretical biology.

[41]  Barbara Banelli,et al.  Epigenetic Targeting of Glioblastoma , 2018, Front. Oncol..

[42]  Shawn M. Gillespie,et al.  Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma , 2014, Science.

[43]  Reid C Thompson,et al.  Inhibition of BET Bromodomain Targets Genetically Diverse Glioblastoma , 2013, Clinical Cancer Research.

[44]  Li Wang,et al.  Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy , 2017, Scientific Reports.

[45]  Mark Bernstein,et al.  Glioma stem cell lines expanded in adherent culture have tumor-specific phenotypes and are suitable for chemical and genetic screens. , 2009, Cell stem cell.

[46]  R. Schneider,et al.  Lateral Thinking: How Histone Modifications Regulate Gene Expression. , 2016, Trends in genetics : TIG.

[47]  Y. Pommier,et al.  Trapping of PARP1 and PARP2 by Clinical PARP Inhibitors. , 2012, Cancer research.

[48]  Anushya Muruganujan,et al.  PANTHER version 11: expanded annotation data from Gene Ontology and Reactome pathways, and data analysis tool enhancements , 2016, Nucleic Acids Res..

[49]  Ian F. Parney,et al.  A novel enhancer regulates MGMT expression and promotes temozolomide resistance in glioblastoma , 2018, Nature Communications.

[50]  S B Green,et al.  Patient age, histologic features, and length of survival in patients with glioblastoma multiforme , 1987, Cancer.

[51]  S. Kwon,et al.  Advances in epigenetic glioblastoma therapy , 2017, Oncotarget.

[52]  S. Berger The complex language of chromatin regulation during transcription , 2007, Nature.

[53]  Yuri Kotliarov,et al.  Tumor stem cells derived from glioblastomas cultured in bFGF and EGF more closely mirror the phenotype and genotype of primary tumors than do serum-cultured cell lines. , 2006, Cancer cell.

[54]  Scar,et al.  Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents. , 2000, The New England journal of medicine.

[55]  Peter A. Jones,et al.  Targeting the cancer epigenome for therapy , 2016, Nature Reviews Genetics.

[56]  Vijayalakshmi Mahadevan,et al.  Targeting the cancer epigenome: synergistic therapy with bromodomain inhibitors. , 2018, Drug discovery today.

[57]  C. Allis,et al.  Translating the Histone Code , 2001, Science.

[58]  David A. Orlando,et al.  Selective Inhibition of Tumor Oncogenes by Disruption of Super-Enhancers , 2013, Cell.

[59]  Neil O Carragher,et al.  High-Content Phenotypic Profiling of Drug Response Signatures across Distinct Cancer Cells , 2010, Molecular Cancer Therapeutics.

[60]  R. Young,et al.  Histone H3K27ac separates active from poised enhancers and predicts developmental state , 2010, Proceedings of the National Academy of Sciences.

[61]  Robert M. Haralick,et al.  Textural Features for Image Classification , 1973, IEEE Trans. Syst. Man Cybern..

[62]  Paul S Mischel,et al.  Maternal embryonic leucine zipper kinase is a key regulator of the proliferation of malignant brain tumors, including brain tumor stem cells , 2008, Journal of neuroscience research.

[63]  Manolis Kellis,et al.  Chromatin Accessibility Impacts Transcriptional Reprogramming in Oocytes , 2018, Cell reports.

[64]  Bruce A. Posner,et al.  Improving drug discovery with high-content phenotypic screens by systematic selection of reporter cell lines , 2015, Nature Biotechnology.

[65]  Zhoulei Li,et al.  BET and HDAC inhibitors induce similar genes and biological effects and synergize to kill in Myc-induced murine lymphoma , 2014, Proceedings of the National Academy of Sciences.

[66]  C. Allis,et al.  Epigenetics: A Landscape Takes Shape , 2007, Cell.

[67]  Steven Pollard,et al.  mTOR inhibition decreases SOX2-SOX9 mediated glioma stem cell activity and temozolomide resistance , 2016, Expert opinion on therapeutic targets.

[68]  Lani F. Wu,et al.  Image-based multivariate profiling of drug responses from single cells , 2007, Nature Methods.

[69]  K. H. Wangenheim,et al.  The role of cell differentiation in controlling cell multiplication and cancer , 2008, Journal of Cancer Research and Clinical Oncology.

[70]  T. Nicolaides,et al.  Bromodomain Inhibitor Review: Bromodomain and Extra-terminal Family Protein Inhibitors as a Potential New Therapy in Central Nervous System Tumors , 2016, Cureus.

[71]  G. Broggi,et al.  Bone morphogenetic proteins inhibit the tumorigenic potential of human brain tumour-initiating cells , 2006, Nature.

[72]  Abraham Nudelman,et al.  In vivo efficacy of a novel histone deacetylase inhibitor in combination with radiation for the treatment of gliomas. , 2007, Neuro-oncology.

[73]  Wolfgang Huber,et al.  A chemical–genetic interaction map of small molecules using high‐throughput imaging in cancer cells , 2015, Molecular systems biology.

[74]  Samuel H. Wilson,et al.  Increased PARP-1 Association with DNA in Alkylation Damaged, PARP-Inhibited Mouse Fibroblasts , 2012, Molecular Cancer Research.

[75]  Wei-Hsiu Liu,et al.  Sox2, a stemness gene, regulates tumor‐initiating and drug‐resistant properties in CD133‐positive glioblastoma stem cells , 2016, Journal of the Chinese Medical Association : JCMA.

[76]  David W Andrews,et al.  A Versatile Cell Death Screening Assay Using Dye-Stained Cells and Multivariate Image Analysis , 2015, Assay and drug development technologies.

[77]  Nicholas A. Hamilton,et al.  Fast automated cell phenotype image classification , 2007, BMC Bioinformatics.