Your browser doesn't support javascript.
loading
Exploring Drug Dosing Regimens In Vitro Using Real-Time 3D Spheroid Tumor Growth Assays.
Lal-Nag, Madhu; McGee, Lauren; Titus, Steven A; Brimacombe, Kyle; Michael, Sam; Sittampalam, Gurusingham; Ferrer, Marc.
Afiliação
  • Lal-Nag M; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • McGee L; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • Titus SA; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • Brimacombe K; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • Michael S; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • Sittampalam G; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
  • Ferrer M; 1 National Center for Advancing Translations Sciences, Division of Preclinical Innovation, National Institutes of Health, Bethesda, MD, USA.
SLAS Discov ; 22(5): 537-546, 2017 06.
Article em En | MEDLINE | ID: mdl-28298153
ABSTRACT
Two-dimensional monolayer cell proliferation assays for cancer drug discovery have made the implementation of large-scale screens feasible but only seem to reflect a simplified view that oncogenes or tumor suppressor genes are the genetic drivers of cancer cell proliferation. However, there is now increased evidence that the cellular and physiological context in which these oncogenic events occur play a key role in how they drive tumor growth in vivo and, therefore, in how tumors respond to drug treatments. In vitro 3D spheroid tumor models are being developed to better mimic the physiology of tumors in vivo, in an attempt to improve the predictability and efficiency of drug discovery for the treatment of cancer. Here we describe the establishment of a real-time 3D spheroid growth, 384-well screening assay. The cells used in this study constitutively expressed green fluorescent protein (GFP), which enabled the real-time monitoring of spheroid formation and the effect of chemotherapeutic agents on spheroid size at different time points of sphere growth and drug treatment. This real-time 3D spheroid assay platform represents a first step toward the replication in vitro of drug dosing regimens being investigated in vivo. We hope that further development of this assay platform will allow the investigation of drug dosing regimens, efficacy, and resistance before preclinical and clinical studies.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios de Seleção de Medicamentos Antitumorais / Esferoides Celulares / Proliferação de Células / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: SLAS Discov Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios de Seleção de Medicamentos Antitumorais / Esferoides Celulares / Proliferação de Células / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: SLAS Discov Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos