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Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine
Cancer still remains a major public health concern around the world and the search for new potential antitumor molecules is essential for fighting the disease. This study evaluated the anticancer and immunomodulatory potential of the newly synthetized ellipticine derivate: sodium bromo-5,11-dimethyl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248987/ https://www.ncbi.nlm.nih.gov/pubmed/32370100 http://dx.doi.org/10.3390/molecules25092130 |
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author | Costa de Oliveira, Regiane Soares Pontes, Gemilson Kostyuk, Aleksandr Coutinho Camargo, Gabriel B. Dhyani, Anamika Shvydenko, Tetiana Shvydenko, Kostiantyn Grafov, Andriy |
author_facet | Costa de Oliveira, Regiane Soares Pontes, Gemilson Kostyuk, Aleksandr Coutinho Camargo, Gabriel B. Dhyani, Anamika Shvydenko, Tetiana Shvydenko, Kostiantyn Grafov, Andriy |
author_sort | Costa de Oliveira, Regiane |
collection | PubMed |
description | Cancer still remains a major public health concern around the world and the search for new potential antitumor molecules is essential for fighting the disease. This study evaluated the anticancer and immunomodulatory potential of the newly synthetized ellipticine derivate: sodium bromo-5,11-dimethyl-6H-pyrido[4,3-b]carbazole-7-sulfonate (Br-Ell-SO(3)Na). It was prepared by the chlorosulfonation of 9-bromoellipticine. The ellipticine-7-sulfonic acid itself is not soluble, but its saponification with sodium hydroxide afforded a water-soluble sodium salt. The cytotoxicity of Br-Ell-SO(3)Na was tested against cancerous (K562 cell line) and non-cancerous cells (Vero cell line and human peripheral blood mononuclear cells (PBMC)) using a Methylthiazoletetrazolium (MTT) assay. Cell cycle arrest was assessed by flow cytometry and the immunomodulatory activity was analyzed through an enzyme-linked immunosorbent assay (ELISA)(.) The results showed that the Br-Ell-SO(3)Na molecule has specific anticancer activity (IC(50) = 35 µM) against the K562 cell line, once no cytotoxicity effect was verified against non-cancerous cells. Cell cycle analysis demonstrated that K562 cells treated with Br-Ell-SO(3)Na were arrested in the phase S. Moreover, the production of IL-6 increased and the expression of IL-8 was inhibited in the human PBMC treated with Br-Ell-SO(3)Na. The results demonstrated that Br-Ell-SO(3)Na is a promising anticancer molecule attested by its noteworthy activity against the K562 tumor cell line and immunomodulatory activity in human PBMC cells. |
format | Online Article Text |
id | pubmed-7248987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72489872020-06-10 Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine Costa de Oliveira, Regiane Soares Pontes, Gemilson Kostyuk, Aleksandr Coutinho Camargo, Gabriel B. Dhyani, Anamika Shvydenko, Tetiana Shvydenko, Kostiantyn Grafov, Andriy Molecules Article Cancer still remains a major public health concern around the world and the search for new potential antitumor molecules is essential for fighting the disease. This study evaluated the anticancer and immunomodulatory potential of the newly synthetized ellipticine derivate: sodium bromo-5,11-dimethyl-6H-pyrido[4,3-b]carbazole-7-sulfonate (Br-Ell-SO(3)Na). It was prepared by the chlorosulfonation of 9-bromoellipticine. The ellipticine-7-sulfonic acid itself is not soluble, but its saponification with sodium hydroxide afforded a water-soluble sodium salt. The cytotoxicity of Br-Ell-SO(3)Na was tested against cancerous (K562 cell line) and non-cancerous cells (Vero cell line and human peripheral blood mononuclear cells (PBMC)) using a Methylthiazoletetrazolium (MTT) assay. Cell cycle arrest was assessed by flow cytometry and the immunomodulatory activity was analyzed through an enzyme-linked immunosorbent assay (ELISA)(.) The results showed that the Br-Ell-SO(3)Na molecule has specific anticancer activity (IC(50) = 35 µM) against the K562 cell line, once no cytotoxicity effect was verified against non-cancerous cells. Cell cycle analysis demonstrated that K562 cells treated with Br-Ell-SO(3)Na were arrested in the phase S. Moreover, the production of IL-6 increased and the expression of IL-8 was inhibited in the human PBMC treated with Br-Ell-SO(3)Na. The results demonstrated that Br-Ell-SO(3)Na is a promising anticancer molecule attested by its noteworthy activity against the K562 tumor cell line and immunomodulatory activity in human PBMC cells. MDPI 2020-05-01 /pmc/articles/PMC7248987/ /pubmed/32370100 http://dx.doi.org/10.3390/molecules25092130 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Costa de Oliveira, Regiane Soares Pontes, Gemilson Kostyuk, Aleksandr Coutinho Camargo, Gabriel B. Dhyani, Anamika Shvydenko, Tetiana Shvydenko, Kostiantyn Grafov, Andriy Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title | Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title_full | Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title_fullStr | Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title_full_unstemmed | Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title_short | Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine |
title_sort | anticancer and immunomodulatory activities of a novel water-soluble derivative of ellipticine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7248987/ https://www.ncbi.nlm.nih.gov/pubmed/32370100 http://dx.doi.org/10.3390/molecules25092130 |
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