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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

In vitro drug sensitivity screens are important tools for discovering anti-cancer drug combinations. Cells grown in spheres activate different signaling pathways and are considered more representative of in vivo models than monolayer cell lines. This protocol describes a method for in vitro drug screening for spheroid lines.

Abstract

In vitro drug sensitivity screens are important tools in the discovery of anti-cancer drug combination therapies. Typically, these in vitro drug screens are performed on cells grown in a monolayer. However, these two-dimensional (2D) models are considered less accurate compared to three-dimensional (3D) spheroid cell models; this is especially true for glioma stem cell lines. Cells grown in spheres activate different signaling pathways and are considered more representative of in vivo models than monolayer cell lines. This protocol describes a method for in vitro drug screening of spheroid lines; mouse and human glioma stem cell lines are used as an example. This protocol describes a 3D spheroid drug sensitivity and synergy assay that can be used to determine if a drug or drug combination induces cell death and if two drugs synergize. Glioma stem cell lines are modified to express RFP. Cells are plated in low attachment round well bottom 96 plates, and spheres are allowed to form overnight. Drugs are added, and the growth is monitored by measuring the RFP signal over time using the Incucyte live imaging system, a fluorescence microscope embedded in the tissue culture incubator. Half maximal inhibitory concentration (IC50), median lethal dose (LD50), and synergy score are subsequently calculated to evaluate sensitivities to drugs alone or in combination. The three-dimensional nature of this assay provides a more accurate reflection of tumor growth, behavior, and drug sensitivities in vivo, thus forming the basis for further preclinical investigation.

Introduction

Glioblastoma is a devastating, high-grade neoplasm of the brain with a 5% five-year overall survival1. High-grade gliomas (HGG) like glioblastoma represent the leading cause of cancer-related mortality in the pediatric population2 and are one of the most recalcitrant tumors to treat in adults as well3. Despite significant advances in our understanding of the molecular drivers of HGG, treatment options remain limited3, emphasizing the need for drug screening methods that more accurately predict therapeutic sensitivities in the clinic.

3D cell cult....

Protocol

All protocol procedures were approved by the Children's Hospital of Philadelphia Institutional Review Board (IRB).

1. 3D spheroid cell plating

  1. Prepare glioma stem cell media: To make the base media, add 50 mL of the proliferation supplement and 5 mL of a 100x penicillin-streptomycin solution (10,000 U/mL) to the basal medium (500 mL). To make glioma stem cell media, add epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) to a final conc.......

Representative Results

As an example, the synergy of Trametinib (MEK inhibitor) and GDC-0941 (PI3K inhibitor), which inhibit two RAS downstream effector pathways in mouse glioma stem cell line 5746 (RFP expressing) was evaluated (Figure 4). Figure 4A shows the same sphere at 0 h and 72 h treated with a combination of Trametinib and GDC-0941. These images were exported directly from the live imager software. IC50 and LD50 were calculated as described in GraphPad (

Discussion

This protocol describes the 3D drug screening assays that have been effectively used to assess drug vulnerabilities in spheroid models of glioma8. This 3D spheroid assay system was specifically designed to allow for a more accurate preclinical investigation of combinatorial chemotherapies for glioma cell lines grown in spheres. For HGG, this method provides a framework for identifying prospective drug vulnerabilities for this devastating disease. However, the potential applications of this system .......

Acknowledgements

None

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Materials

NameCompanyCatalog NumberComments
15 mL centrifugation tubesCELLTREAT22941115 mL polypropylene centrifuge tubes, sterile
96- well plateS-bioMS9096UZ96-well round-bottom ultra-low attachment plate
AccutaseSTEMCELL Technologies7922Cell detachment solution
Acridine Orange/Propidium Iodide StainLogos BiosystemsF23001Live/dead stain for cell counting
bFGFSTEMCELL Technologies78003.2Human recombinant bFGF
Cell CounterLogos BiosystemsL20001LUNA-FL Dual Fluorescence Cell Counter
CentrifugeEppendorf5810RCentrifuging cells and plates
DMSOPierce20688solvent for compounds
EGFSTEMCELL Technologies78006.2Human recombinant EGF
Eppendorf tubesCostar07-200-534Microcentrifuge tubes
ExcelMicrosoftMicrosoft excel
GDC-0941SelleckchemS1065Drug 1
GraphPadGraphPadGraphPad Prism 9Calculation of IC50 and LD50
HemocytometerLogos BiosystemsLGBD10008Luna PhotonSlide
IncucyteSartoriusS3Fluorescence microscope embedded in the tissue culture incubator that images every well at specific time intervals.
Incucyte softwareSartoriusIncucyte 2022BAnalysis of proliferation data
MediaSTEMCELL Technologies5702NeuroCult (Mouse and Rat) proliferation kit containging Basal Medium and growth supplement
Penicillin-Streptomycin Gibco15140122Antibiotics to add to media
TrametinibSelleckchemS2673Drug 2

References

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In Vitro Drug Screening3D SpheroidGlioma Stem Cell LinesRFPDrug SensitivityDrug SynergyIC50LD50Incucyte Live Imaging

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