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Multiplexed Live-Cell Imaging for Drug Responses in Patient-Derived Organoid Models of Cancer.
Colling, Kaitriana E; Symons, Emily L; Buroni, Lorenzo; Sumanasiri, Hiruni K; Andrew-Udoh, Jessica; Witt, Emily; Losh, Haley A; Morrison, Abigail M; Leslie, Kimberly K; Dunnill, Christopher J; de Bono, Johann S; Thiel, Kristina W.
Affiliation
  • Colling KE; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa; Cancer Biology Graduate Program, Carver College of Medicine, University of Iowa.
  • Symons EL; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa.
  • Buroni L; The Institute of Cancer Research: and the Royal Marsden NHS Foundation Trust.
  • Sumanasiri HK; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa.
  • Andrew-Udoh J; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa.
  • Witt E; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa; Department of Radiation Oncology, Carver College of Medicine, University of Iowa.
  • Losh HA; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa.
  • Morrison AM; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa.
  • Leslie KK; Division of Molecular Medicine, Departments of Internal Medicine and Obstetrics and Gynecology, University of New Mexico Comprehensive Cancer Center, University of New Mexico Health Sciences Center.
  • Dunnill CJ; Agilent Technologies.
  • de Bono JS; The Institute of Cancer Research: and the Royal Marsden NHS Foundation Trust.
  • Thiel KW; Department of Obstetrics and Gynecology, Carver College of Medicine, University of Iowa; Holden Comprehensive Cancer Center, University of Iowa; kristina-thiel@uiowa.edu.
J Vis Exp ; (203)2024 Jan 05.
Article in En | MEDLINE | ID: mdl-38251777
ABSTRACT
Patient-derived organoid (PDO) models of cancer are a multifunctional research system that better recapitulates human disease as compared to cancer cell lines. PDO models can be generated by culturing patient tumor cells in extracellular basement membrane extracts (BME) and plating them as three-dimensional domes. However, commercially available reagents that have been optimized for phenotypic assays in monolayer cultures often are not compatible with BME. Herein, we describe a method to plate PDO models and assess drug effects using an automated live-cell imaging system. In addition, we apply fluorescent dyes that are compatible with kinetic measurements to quantify cell health and apoptosis simultaneously. Image capture can be customized to occur at regular time intervals over several days. Users can analyze drug effects in individual Z-plane images or a Z Projection of serial images from multiple focal planes. Using masking, specific parameters of interest are calculated, such as PDO number, area, and fluorescence intensity. We provide proof-of-concept data demonstrating the effect of cytotoxic agents on cell health, apoptosis, and viability. This automated kinetic imaging platform can be expanded to other phenotypic readouts to understand diverse therapeutic effects in PDO models of cancer.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Neoplasms Limits: Humans Language: En Journal: J Vis Exp Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Neoplasms Limits: Humans Language: En Journal: J Vis Exp Year: 2024 Type: Article