Abstract

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.

Highlights

  • One of the greatest challenges in drug discovery and development is understanding how seemingly identical cells respond differently to drug treatment [1]

  • Cellular heterogeneity is not limited to cancer cells, but is exhibited even in normal, clonal cell lines, and the impact of heterogeneity extends from basic biology to drug discovery and diagnostics [9,10,11]

  • Characterization of heterogeneity in High Content Screening (HCS) We optimized the assay and performed an HCS screen to measure the activation of the STAT3 signaling pathway in response to interleukin 6 (IL-6) and/or Oncostatin M (OSM) using an antibody against phospho-STAT3-Y705 [49]

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Summary

Introduction

One of the greatest challenges in drug discovery and development is understanding how seemingly identical cells respond differently to drug treatment [1]. Intrinsic heterogeneity arises from intracellular factors, even in a uniform environment, and can be further subdivided into macro- and micro-heterogeneity [9] The former refers to the variability in one or more cell traits that result in discrete phenotypes and the latter to the apparently continuous random variation within a single phenotype. It is widely accepted that non-genetic heterogeneity plays an important biological role in cell behaviors such as cell fate decision in stem cells, development and cellular physiology [9,10,11] It is of increasing interest in tumor diagnostics, therapeutics and disease management, as well as drug discovery and development [14,15,16,17]

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