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COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo
Identification of novel anti-cancer compounds with high efficacy and low toxicity is critical in drug development. High-throughput screening and other such strategies are generally resource-intensive. Therefore, in silico computer-aided drug design has gained rapid acceptance and popularity. We empl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173065/ https://www.ncbi.nlm.nih.gov/pubmed/27150056 http://dx.doi.org/10.18632/oncotarget.9133 |
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author | Salim, Kowthar Y. Vareki, Saman Maleki Danter, Wayne R. Koropatnick, James |
author_facet | Salim, Kowthar Y. Vareki, Saman Maleki Danter, Wayne R. Koropatnick, James |
author_sort | Salim, Kowthar Y. |
collection | PubMed |
description | Identification of novel anti-cancer compounds with high efficacy and low toxicity is critical in drug development. High-throughput screening and other such strategies are generally resource-intensive. Therefore, in silico computer-aided drug design has gained rapid acceptance and popularity. We employed our proprietary computational platform (CHEMSAS(®)), which uses a unique combination of traditional and modern pharmacology principles, statistical modeling, medicinal chemistry, and machine-learning technologies to discover and optimize novel compounds that could target various cancers. COTI-2 is a small molecule candidate anti-cancer drug identified using CHEMSAS. This study describes the in vitro and in vivo evaluation of COTI-2. Our data demonstrate that COTI-2 is effective against a diverse group of human cancer cell lines regardless of their tissue of origin or genetic makeup. Most treated cancer cell lines were sensitive to COTI-2 at nanomolar concentrations. When compared to traditional chemotherapy or targeted-therapy agents, COTI-2 showed superior activity against tumor cells, in vitro and in vivo. Despite its potent anti-tumor efficacy, COTI-2 was safe and well-tolerated in vivo. Although the mechanism of action of COTI-2 is still under investigation, preliminary results indicate that it is not a traditional kinase or an Hsp90 inhibitor. |
format | Online Article Text |
id | pubmed-5173065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-51730652016-12-23 COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo Salim, Kowthar Y. Vareki, Saman Maleki Danter, Wayne R. Koropatnick, James Oncotarget Research Paper Identification of novel anti-cancer compounds with high efficacy and low toxicity is critical in drug development. High-throughput screening and other such strategies are generally resource-intensive. Therefore, in silico computer-aided drug design has gained rapid acceptance and popularity. We employed our proprietary computational platform (CHEMSAS(®)), which uses a unique combination of traditional and modern pharmacology principles, statistical modeling, medicinal chemistry, and machine-learning technologies to discover and optimize novel compounds that could target various cancers. COTI-2 is a small molecule candidate anti-cancer drug identified using CHEMSAS. This study describes the in vitro and in vivo evaluation of COTI-2. Our data demonstrate that COTI-2 is effective against a diverse group of human cancer cell lines regardless of their tissue of origin or genetic makeup. Most treated cancer cell lines were sensitive to COTI-2 at nanomolar concentrations. When compared to traditional chemotherapy or targeted-therapy agents, COTI-2 showed superior activity against tumor cells, in vitro and in vivo. Despite its potent anti-tumor efficacy, COTI-2 was safe and well-tolerated in vivo. Although the mechanism of action of COTI-2 is still under investigation, preliminary results indicate that it is not a traditional kinase or an Hsp90 inhibitor. Impact Journals LLC 2016-05-02 /pmc/articles/PMC5173065/ /pubmed/27150056 http://dx.doi.org/10.18632/oncotarget.9133 Text en Copyright: © 2016 Salim et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Salim, Kowthar Y. Vareki, Saman Maleki Danter, Wayne R. Koropatnick, James COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title | COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title_full | COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title_fullStr | COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title_full_unstemmed | COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title_short | COTI-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
title_sort | coti-2, a novel small molecule that is active against multiple human cancer cell lines in vitro and in vivo |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173065/ https://www.ncbi.nlm.nih.gov/pubmed/27150056 http://dx.doi.org/10.18632/oncotarget.9133 |
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