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Identifying and quantifying heterogeneity in high content analysis: application of heterogeneity indices to drug discovery.
Gough, Albert H; Chen, Ning; Shun, Tong Ying; Lezon, Timothy R; Boltz, Robert C; Reese, Celeste E; Wagner, Jacob; Vernetti, Lawrence A; Grandis, Jennifer R; Lee, Adrian V; Stern, Andrew M; Schurdak, Mark E; Taylor, D Lansing.
Afiliação
  • Gough AH; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Chen N; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Shun TY; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Lezon TR; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Boltz RC; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Reese CE; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Wagner J; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Vernetti LA; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Grandis JR; University of Pittsburgh Cancer Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Otolaryngology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Pharmacology and Chemical Biology, University of Pittsbur
  • Lee AV; University of Pittsburgh Cancer Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Pharmacology and Chemical Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Stern AM; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Schurdak ME; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; University of Pittsburgh Cancer Institute, University of Pittsburgh
  • Taylor DL; Drug Discovery Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; Department of Computational & Systems Biology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America; University of Pittsburgh Cancer Institute, University of Pittsburgh
PLoS One ; 9(7): e102678, 2014.
Article em En | MEDLINE | ID: mdl-25036749
One of the greatest challenges in biomedical research, drug discovery and diagnostics is understanding how seemingly identical cells can respond differently to perturbagens including drugs for disease treatment. Although heterogeneity has become an accepted characteristic of a population of cells, in drug discovery it is not routinely evaluated or reported. The standard practice for cell-based, high content assays has been to assume a normal distribution and to report a well-to-well average value with a standard deviation. To address this important issue we sought to define a method that could be readily implemented to identify, quantify and characterize heterogeneity in cellular and small organism assays to guide decisions during drug discovery and experimental cell/tissue profiling. Our study revealed that heterogeneity can be effectively identified and quantified with three indices that indicate diversity, non-normality and percent outliers. The indices were evaluated using the induction and inhibition of STAT3 activation in five cell lines where the systems response including sample preparation and instrument performance were well characterized and controlled. These heterogeneity indices provide a standardized method that can easily be integrated into small and large scale screening or profiling projects to guide interpretation of the biology, as well as the development of therapeutics and diagnostics. Understanding the heterogeneity in the response to perturbagens will become a critical factor in designing strategies for the development of therapeutics including targeted polypharmacology.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Descoberta de Drogas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: PLoS One Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Descoberta de Drogas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: PLoS One Ano de publicação: 2014 Tipo de documento: Article