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Evaluation of In Vivo Biological Activity Profiles of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and Histopathology Studies
[Image: see text] The anticancer activity of N-benzylisoindole-1,3-dione derivatives was evaluated against adenocarcinoma (A549-Luc). First, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide activity assay studies of two isoindole-1,3-dione derivatives were performed against A549 cell lin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077444/ https://www.ncbi.nlm.nih.gov/pubmed/37033818 http://dx.doi.org/10.1021/acsomega.3c00560 |
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author | Köse, Aytekin Kaya, Meltem Tomruk, Canberk Uyanıkgil, Yiǧit Kishalı, Nurhan Kara, Yunus Şanlı-Mohamed, Gülşah |
author_facet | Köse, Aytekin Kaya, Meltem Tomruk, Canberk Uyanıkgil, Yiǧit Kishalı, Nurhan Kara, Yunus Şanlı-Mohamed, Gülşah |
author_sort | Köse, Aytekin |
collection | PubMed |
description | [Image: see text] The anticancer activity of N-benzylisoindole-1,3-dione derivatives was evaluated against adenocarcinoma (A549-Luc). First, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide activity assay studies of two isoindole-1,3-dione derivatives were performed against A549 cell lines. Both compounds showed inhibitory effects on the viability of A549 cells. Then, we explored the potential of these compounds as active ingredients by in vivo studies. Nude mice were given A549-luc lung cancer cells, and tumor growth was induced with a xenograft model. Then, nude mice were divided into three groups: the control group, compound 3 group, and compound 4 group. After application of each compound to the mice, tumor sizes, their survival, and weight were determined for 60 days. Furthermore, toxicological studies were performed to examine the effects of the drugs in mice. In addition to toxicological studies, histopathological analyses of organs taken from mice were performed, and the results were evaluated. The obtained results showed that both N-benzylisoindole derivatives are potential anticancer agents. |
format | Online Article Text |
id | pubmed-10077444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100774442023-04-07 Evaluation of In Vivo Biological Activity Profiles of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and Histopathology Studies Köse, Aytekin Kaya, Meltem Tomruk, Canberk Uyanıkgil, Yiǧit Kishalı, Nurhan Kara, Yunus Şanlı-Mohamed, Gülşah ACS Omega [Image: see text] The anticancer activity of N-benzylisoindole-1,3-dione derivatives was evaluated against adenocarcinoma (A549-Luc). First, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide activity assay studies of two isoindole-1,3-dione derivatives were performed against A549 cell lines. Both compounds showed inhibitory effects on the viability of A549 cells. Then, we explored the potential of these compounds as active ingredients by in vivo studies. Nude mice were given A549-luc lung cancer cells, and tumor growth was induced with a xenograft model. Then, nude mice were divided into three groups: the control group, compound 3 group, and compound 4 group. After application of each compound to the mice, tumor sizes, their survival, and weight were determined for 60 days. Furthermore, toxicological studies were performed to examine the effects of the drugs in mice. In addition to toxicological studies, histopathological analyses of organs taken from mice were performed, and the results were evaluated. The obtained results showed that both N-benzylisoindole derivatives are potential anticancer agents. American Chemical Society 2023-03-21 /pmc/articles/PMC10077444/ /pubmed/37033818 http://dx.doi.org/10.1021/acsomega.3c00560 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Köse, Aytekin Kaya, Meltem Tomruk, Canberk Uyanıkgil, Yiǧit Kishalı, Nurhan Kara, Yunus Şanlı-Mohamed, Gülşah Evaluation of In Vivo Biological Activity Profiles of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and Histopathology Studies |
title | Evaluation of In Vivo Biological Activity Profiles
of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and
Histopathology Studies |
title_full | Evaluation of In Vivo Biological Activity Profiles
of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and
Histopathology Studies |
title_fullStr | Evaluation of In Vivo Biological Activity Profiles
of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and
Histopathology Studies |
title_full_unstemmed | Evaluation of In Vivo Biological Activity Profiles
of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and
Histopathology Studies |
title_short | Evaluation of In Vivo Biological Activity Profiles
of Isoindole-1,3-dione Derivatives: Cytotoxicity, Toxicology, and
Histopathology Studies |
title_sort | evaluation of in vivo biological activity profiles
of isoindole-1,3-dione derivatives: cytotoxicity, toxicology, and
histopathology studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077444/ https://www.ncbi.nlm.nih.gov/pubmed/37033818 http://dx.doi.org/10.1021/acsomega.3c00560 |
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