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Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy

The Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) regulates the expression of various critical mediators of cancer and is considered as one of the central communication nodes in cell growth and survival. Marine natural products (MNP) represent great resources for disc...

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Autores principales: Li, Rui, Zhou, Yue, Zhang, Xinxin, Yang, Lujia, Liu, Jieyu, Wightman, Samantha M., Lv, Ling, Liu, Zhiqing, Wang, Chang-Yun, Zhao, Chenyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077262/
https://www.ncbi.nlm.nih.gov/pubmed/37073329
http://dx.doi.org/10.1007/s42995-022-00162-x
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author Li, Rui
Zhou, Yue
Zhang, Xinxin
Yang, Lujia
Liu, Jieyu
Wightman, Samantha M.
Lv, Ling
Liu, Zhiqing
Wang, Chang-Yun
Zhao, Chenyang
author_facet Li, Rui
Zhou, Yue
Zhang, Xinxin
Yang, Lujia
Liu, Jieyu
Wightman, Samantha M.
Lv, Ling
Liu, Zhiqing
Wang, Chang-Yun
Zhao, Chenyang
author_sort Li, Rui
collection PubMed
description The Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) regulates the expression of various critical mediators of cancer and is considered as one of the central communication nodes in cell growth and survival. Marine natural products (MNP) represent great resources for discovery of bioactive lead compounds, especially anti-cancer agents. Through the medium-throughput screening of our in-house MNP library, Pretrichodermamide B, an epidithiodiketopiperazine, was identified as a JAK/STAT3 signaling inhibitor. Further studies identified that Pretrichodermamide B directly binds to STAT3, preventing phosphorylation and thus inhibiting JAK/STAT3 signaling. Moreover, it suppressed cancer cell growth, in vitro, at low micromolar concentrations and demonstrated efficacy in vivo by decreasing tumor growth in a xenograft mouse model. In addition, it was shown that Pretrichodermamide B was able to induce cell cycle arrest and promote cell apoptosis. This study demonstrated that Pretrichodermamide B is a novel STAT3 inhibitor, which should be considered for further exploration as a promising anti-cancer therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-022-00162-x.
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spelling pubmed-100772622023-04-17 Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy Li, Rui Zhou, Yue Zhang, Xinxin Yang, Lujia Liu, Jieyu Wightman, Samantha M. Lv, Ling Liu, Zhiqing Wang, Chang-Yun Zhao, Chenyang Mar Life Sci Technol Research Paper The Janus kinase (JAK)/signal transducer and activator of transcription 3 (STAT3) regulates the expression of various critical mediators of cancer and is considered as one of the central communication nodes in cell growth and survival. Marine natural products (MNP) represent great resources for discovery of bioactive lead compounds, especially anti-cancer agents. Through the medium-throughput screening of our in-house MNP library, Pretrichodermamide B, an epidithiodiketopiperazine, was identified as a JAK/STAT3 signaling inhibitor. Further studies identified that Pretrichodermamide B directly binds to STAT3, preventing phosphorylation and thus inhibiting JAK/STAT3 signaling. Moreover, it suppressed cancer cell growth, in vitro, at low micromolar concentrations and demonstrated efficacy in vivo by decreasing tumor growth in a xenograft mouse model. In addition, it was shown that Pretrichodermamide B was able to induce cell cycle arrest and promote cell apoptosis. This study demonstrated that Pretrichodermamide B is a novel STAT3 inhibitor, which should be considered for further exploration as a promising anti-cancer therapy. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s42995-022-00162-x. Springer Nature Singapore 2023-02-06 /pmc/articles/PMC10077262/ /pubmed/37073329 http://dx.doi.org/10.1007/s42995-022-00162-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Paper
Li, Rui
Zhou, Yue
Zhang, Xinxin
Yang, Lujia
Liu, Jieyu
Wightman, Samantha M.
Lv, Ling
Liu, Zhiqing
Wang, Chang-Yun
Zhao, Chenyang
Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title_full Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title_fullStr Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title_full_unstemmed Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title_short Identification of marine natural product Pretrichodermamide B as a STAT3 inhibitor for efficient anticancer therapy
title_sort identification of marine natural product pretrichodermamide b as a stat3 inhibitor for efficient anticancer therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10077262/
https://www.ncbi.nlm.nih.gov/pubmed/37073329
http://dx.doi.org/10.1007/s42995-022-00162-x
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