| Literature DB >> 29345979 |
Eoghan O'Duibhir1, Jasmin Paris1, Hannah Lawson1, Catarina Sepulveda1, Dahlia Doughty Shenton2, Neil O Carragher3, Kamil R Kranc1,3.
Abstract
There is a large amount of information in brightfield images that was previously inaccessible by using traditional microscopy techniques. This information can now be exploited by using machine-learning approaches for both image segmentation and the classification of objects. We have combined these approaches with a label-free assay for growth and differentiation of leukemic colonies, to generate a novel platform for phenotypic drug discovery. Initially, a supervised machine-learning algorithm was used to identify in-focus colonies growing in a three-dimensional (3D) methylcellulose gel. Once identified, unsupervised clustering and principle component analysis of texture-based phenotypic profiles were applied to group similar phenotypes. In a proof-of-concept study, we successfully identified a novel phenotype induced by a compound that is currently in clinical trials for the treatment of leukemia. We believe that our platform will be of great benefit for the utilization of patient-derived 3D cell culture systems for both drug discovery and diagnostic applications.Entities:
Keywords: 3D; epigenetic; high content; leukemia; machine learning; phenotypic
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Year: 2018 PMID: 29345979 DOI: 10.1089/adt.2017.819
Source DB: PubMed Journal: Assay Drug Dev Technol ISSN: 1540-658X Impact factor: 1.738