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Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo

Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytotoxicity against of a panel of various cancer cell lines. They were shown to be more sensitive to S180 and H22 tumor cells with IC(50) values ranging from 1.01–3.65 μM, and distinctly were more cytotoxi...

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Detalles Bibliográficos
Autores principales: Li, Dongdong, Dai, Linlin, Zhao, Xiumei, Zhi, Shuang, Shen, Hongsheng, Yang, Zibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222802/
https://www.ncbi.nlm.nih.gov/pubmed/30082625
http://dx.doi.org/10.3390/molecules23081960
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author Li, Dongdong
Dai, Linlin
Zhao, Xiumei
Zhi, Shuang
Shen, Hongsheng
Yang, Zibo
author_facet Li, Dongdong
Dai, Linlin
Zhao, Xiumei
Zhi, Shuang
Shen, Hongsheng
Yang, Zibo
author_sort Li, Dongdong
collection PubMed
description Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytotoxicity against of a panel of various cancer cell lines. They were shown to be more sensitive to S180 and H22 tumor cells with IC(50) values ranging from 1.01–3.65 μM, and distinctly were more cytotoxic to cancer cells than normal cell L929. In addition, compounds 7a, 7c, and 7e displayed moderate tumor suppression without apparent organ toxicity in vivo against mice bearing H22 liver tumors. Furthermore, they arrested tumor cells in the G1 phase and induced cellular apoptosis. Their potential binding modes with DNA-Top I complex have also been investigated.
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spelling pubmed-62228022018-11-13 Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo Li, Dongdong Dai, Linlin Zhao, Xiumei Zhi, Shuang Shen, Hongsheng Yang, Zibo Molecules Article Novel mustard functionalized sophoridine derivatives were synthesized and evaluated for their cytotoxicity against of a panel of various cancer cell lines. They were shown to be more sensitive to S180 and H22 tumor cells with IC(50) values ranging from 1.01–3.65 μM, and distinctly were more cytotoxic to cancer cells than normal cell L929. In addition, compounds 7a, 7c, and 7e displayed moderate tumor suppression without apparent organ toxicity in vivo against mice bearing H22 liver tumors. Furthermore, they arrested tumor cells in the G1 phase and induced cellular apoptosis. Their potential binding modes with DNA-Top I complex have also been investigated. MDPI 2018-08-06 /pmc/articles/PMC6222802/ /pubmed/30082625 http://dx.doi.org/10.3390/molecules23081960 Text en © 2018 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
Li, Dongdong
Dai, Linlin
Zhao, Xiumei
Zhi, Shuang
Shen, Hongsheng
Yang, Zibo
Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title_full Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title_fullStr Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title_full_unstemmed Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title_short Novel Sophoridine Derivatives Bearing Phosphoramide Mustard Moiety Exhibit Potent Antitumor Activities In Vitro and In Vivo
title_sort novel sophoridine derivatives bearing phosphoramide mustard moiety exhibit potent antitumor activities in vitro and in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222802/
https://www.ncbi.nlm.nih.gov/pubmed/30082625
http://dx.doi.org/10.3390/molecules23081960
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