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Development of a Rapid In Vitro Screening Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer Agents
[Image: see text] Traditional long exposure (24–72 h) cell viability assays for identification of potential drug compounds can fail to identify compounds that are: (a) biologically active but not toxic and (b) inactive without the addition of a synergistic additive. Herein, we report the development...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296616/ https://www.ncbi.nlm.nih.gov/pubmed/34308064 http://dx.doi.org/10.1021/acsomega.1c02203 |
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author | Abebe, Felagot A. Hopkins, Megan D. Vodnala, Suraj N. Sheaff, Robert J. Lamar, Angus A. |
author_facet | Abebe, Felagot A. Hopkins, Megan D. Vodnala, Suraj N. Sheaff, Robert J. Lamar, Angus A. |
author_sort | Abebe, Felagot A. |
collection | PubMed |
description | [Image: see text] Traditional long exposure (24–72 h) cell viability assays for identification of potential drug compounds can fail to identify compounds that are: (a) biologically active but not toxic and (b) inactive without the addition of a synergistic additive. Herein, we report the development of a rapid (1–2 h) compound screening technique using a commercially available cell viability kit (CellTiter-Glo) that has led to the detection of compounds that were not identified as active agents using traditional cytotoxicity screening methods. These compounds, in combination with metabolic inhibitor 2-deoxyglucose, display selectivity toward a pancreatic cancer cell line. An evaluation of 11 mammalian cell lines against 30 novel compounds and two metabolic inhibitors is reported. The inclusion of metabolic inhibitors during an initial screening process, and not simply during mechanistic investigations of a previously identified hit compound, provides a rapid and sensitive tool for identifying drug candidates potentially overlooked by other methods. |
format | Online Article Text |
id | pubmed-8296616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82966162021-07-23 Development of a Rapid In Vitro Screening Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer Agents Abebe, Felagot A. Hopkins, Megan D. Vodnala, Suraj N. Sheaff, Robert J. Lamar, Angus A. ACS Omega [Image: see text] Traditional long exposure (24–72 h) cell viability assays for identification of potential drug compounds can fail to identify compounds that are: (a) biologically active but not toxic and (b) inactive without the addition of a synergistic additive. Herein, we report the development of a rapid (1–2 h) compound screening technique using a commercially available cell viability kit (CellTiter-Glo) that has led to the detection of compounds that were not identified as active agents using traditional cytotoxicity screening methods. These compounds, in combination with metabolic inhibitor 2-deoxyglucose, display selectivity toward a pancreatic cancer cell line. An evaluation of 11 mammalian cell lines against 30 novel compounds and two metabolic inhibitors is reported. The inclusion of metabolic inhibitors during an initial screening process, and not simply during mechanistic investigations of a previously identified hit compound, provides a rapid and sensitive tool for identifying drug candidates potentially overlooked by other methods. American Chemical Society 2021-07-02 /pmc/articles/PMC8296616/ /pubmed/34308064 http://dx.doi.org/10.1021/acsomega.1c02203 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Abebe, Felagot A. Hopkins, Megan D. Vodnala, Suraj N. Sheaff, Robert J. Lamar, Angus A. Development of a Rapid In Vitro Screening Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer Agents |
title | Development of a Rapid In Vitro Screening
Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer
Agents |
title_full | Development of a Rapid In Vitro Screening
Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer
Agents |
title_fullStr | Development of a Rapid In Vitro Screening
Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer
Agents |
title_full_unstemmed | Development of a Rapid In Vitro Screening
Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer
Agents |
title_short | Development of a Rapid In Vitro Screening
Assay Using Metabolic Inhibitors to Detect Highly Selective Anticancer
Agents |
title_sort | development of a rapid in vitro screening
assay using metabolic inhibitors to detect highly selective anticancer
agents |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296616/ https://www.ncbi.nlm.nih.gov/pubmed/34308064 http://dx.doi.org/10.1021/acsomega.1c02203 |
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