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Novel harmine derivatives for tumor targeted therapy

Harmine is a beta-carboline alkaloid found in medicinal plant PeganumHarmala, which has served as a folk anticancer medicine. However, clinical applications of harmine were limited by its low pharmacological effects and noticeable neurotoxicity. In this study, we modified harmine to increase the the...

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Autores principales: Li, Siwen, Wang, Aqin, Gu, Fan, Wang, Zhaohui, Tian, Caiping, Qian, Zhiyu, Tang, Liping, Gu, Yueqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496197/
https://www.ncbi.nlm.nih.gov/pubmed/25940702
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author Li, Siwen
Wang, Aqin
Gu, Fan
Wang, Zhaohui
Tian, Caiping
Qian, Zhiyu
Tang, Liping
Gu, Yueqing
author_facet Li, Siwen
Wang, Aqin
Gu, Fan
Wang, Zhaohui
Tian, Caiping
Qian, Zhiyu
Tang, Liping
Gu, Yueqing
author_sort Li, Siwen
collection PubMed
description Harmine is a beta-carboline alkaloid found in medicinal plant PeganumHarmala, which has served as a folk anticancer medicine. However, clinical applications of harmine were limited by its low pharmacological effects and noticeable neurotoxicity. In this study, we modified harmine to increase the therapeutic efficacy and to decrease the systemic toxicity. Specifically, two tumor targeting harmine derivatives 2DG-Har-01 and MET-Har-02 were synthesized by modifying substituent in position-2, -7 and -9 of harmine ring with two different targeting group2-amino-2-deoxy-D-glucose (2DG) and Methionine (Met), respectively. Their therapeutic efficacy and toxicity were investigated both in vitro and in vivo. Results suggested that the two newharmine derivatives displayed much higher therapeutic effects than non-modified harmine. In particular, MET-Har-02 was more potent than 2DG-Har-01 with promising potential for targeted cancer therapy.
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spelling pubmed-44961972015-07-10 Novel harmine derivatives for tumor targeted therapy Li, Siwen Wang, Aqin Gu, Fan Wang, Zhaohui Tian, Caiping Qian, Zhiyu Tang, Liping Gu, Yueqing Oncotarget Research Paper Harmine is a beta-carboline alkaloid found in medicinal plant PeganumHarmala, which has served as a folk anticancer medicine. However, clinical applications of harmine were limited by its low pharmacological effects and noticeable neurotoxicity. In this study, we modified harmine to increase the therapeutic efficacy and to decrease the systemic toxicity. Specifically, two tumor targeting harmine derivatives 2DG-Har-01 and MET-Har-02 were synthesized by modifying substituent in position-2, -7 and -9 of harmine ring with two different targeting group2-amino-2-deoxy-D-glucose (2DG) and Methionine (Met), respectively. Their therapeutic efficacy and toxicity were investigated both in vitro and in vivo. Results suggested that the two newharmine derivatives displayed much higher therapeutic effects than non-modified harmine. In particular, MET-Har-02 was more potent than 2DG-Har-01 with promising potential for targeted cancer therapy. Impact Journals LLC 2015-04-22 /pmc/articles/PMC4496197/ /pubmed/25940702 Text en Copyright: © 2015 Li 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
Li, Siwen
Wang, Aqin
Gu, Fan
Wang, Zhaohui
Tian, Caiping
Qian, Zhiyu
Tang, Liping
Gu, Yueqing
Novel harmine derivatives for tumor targeted therapy
title Novel harmine derivatives for tumor targeted therapy
title_full Novel harmine derivatives for tumor targeted therapy
title_fullStr Novel harmine derivatives for tumor targeted therapy
title_full_unstemmed Novel harmine derivatives for tumor targeted therapy
title_short Novel harmine derivatives for tumor targeted therapy
title_sort novel harmine derivatives for tumor targeted therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496197/
https://www.ncbi.nlm.nih.gov/pubmed/25940702
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