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Shikonin inhibits cancer cell cycling by targeting Cdc25s

BACKGROUND: Shikonin, a natural naphthoquinone, is abundant in Chinese herb medicine Zicao (purple gromwell) and has a wide range of biological activities, especially for cancer. Shikonin and its analogues have been reported to induce cell-cycle arrest, but target information is still unclear. We hy...

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Autores principales: Zhang, Shoude, Gao, Qiang, Li, Wei, Zhu, Luwei, Shang, Qianhan, Feng, Shuo, Jia, Junmei, Jia, Qiangqiang, Shen, Shuo, Su, Zhanhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323793/
https://www.ncbi.nlm.nih.gov/pubmed/30616572
http://dx.doi.org/10.1186/s12885-018-5220-x
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author Zhang, Shoude
Gao, Qiang
Li, Wei
Zhu, Luwei
Shang, Qianhan
Feng, Shuo
Jia, Junmei
Jia, Qiangqiang
Shen, Shuo
Su, Zhanhai
author_facet Zhang, Shoude
Gao, Qiang
Li, Wei
Zhu, Luwei
Shang, Qianhan
Feng, Shuo
Jia, Junmei
Jia, Qiangqiang
Shen, Shuo
Su, Zhanhai
author_sort Zhang, Shoude
collection PubMed
description BACKGROUND: Shikonin, a natural naphthoquinone, is abundant in Chinese herb medicine Zicao (purple gromwell) and has a wide range of biological activities, especially for cancer. Shikonin and its analogues have been reported to induce cell-cycle arrest, but target information is still unclear. We hypothesized that shikonin, with a structure similar to that of quinone-type compounds, which are inhibitors of cell division cycle 25 (Cdc25) phosphatases, will have similar effects on Cdc25s. To test this hypothesis, the effects of shikonin on Cdc25s and cell-cycle progression were determined in this paper. METHODS: The in vitro effects of shikonin and its analogues on Cdc25s were detected by fluorometric assay kit. The binding mode between shikonin and Cdc25B was modelled by molecular docking. The dephosphorylating level of cyclin-dependent kinase 1 (CDK1), a natural substrate of Cdc25B, was tested by Western blotting. The effect of shikonin on cell cycle progression was investigated by flow cytometry analysis. We also tested the anti-proliferation activity of shikonin on cancer cell lines by MTT assay. Moreover, in vivo anti-proliferation activity was tested in a mouse xenograft tumour model. RESULTS: Shikonin and its analogues inhibited recombinant human Cdc25 A, B, and C phosphatase with IC(50) values ranging from 2.14 ± 0.21 to 13.45 ± 1.45 μM irreversibly. The molecular modelling results showed that shikonin bound to the inhibitor binding pocket of Cdc25B with a favourable binding mode through hydrophobic interactions and hydrogen bonds. In addition, an accumulation of the tyrosine 15-phosphorylated form of CDK1 was induced by shikonin in a concentration-dependent manner in vitro and in vivo. We also confirmed that shikonin showed an anti-proliferation effect on three cancer cell lines with IC(50) values ranging from 6.15 ± 0.46 to 9.56 ± 1.03 μM. Furthermore, shikonin showed a promising anti-proliferation effect on a K562 mouse xenograph tumour model. CONCLUSION: In this study, we provide evidence for how shikonin induces cell cycle arrest and functions as a Cdc25s inhibitor. It shows an anti-proliferation effect both in vitro and in vivo by mediating Cdc25s.
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spelling pubmed-63237932019-01-11 Shikonin inhibits cancer cell cycling by targeting Cdc25s Zhang, Shoude Gao, Qiang Li, Wei Zhu, Luwei Shang, Qianhan Feng, Shuo Jia, Junmei Jia, Qiangqiang Shen, Shuo Su, Zhanhai BMC Cancer Research Article BACKGROUND: Shikonin, a natural naphthoquinone, is abundant in Chinese herb medicine Zicao (purple gromwell) and has a wide range of biological activities, especially for cancer. Shikonin and its analogues have been reported to induce cell-cycle arrest, but target information is still unclear. We hypothesized that shikonin, with a structure similar to that of quinone-type compounds, which are inhibitors of cell division cycle 25 (Cdc25) phosphatases, will have similar effects on Cdc25s. To test this hypothesis, the effects of shikonin on Cdc25s and cell-cycle progression were determined in this paper. METHODS: The in vitro effects of shikonin and its analogues on Cdc25s were detected by fluorometric assay kit. The binding mode between shikonin and Cdc25B was modelled by molecular docking. The dephosphorylating level of cyclin-dependent kinase 1 (CDK1), a natural substrate of Cdc25B, was tested by Western blotting. The effect of shikonin on cell cycle progression was investigated by flow cytometry analysis. We also tested the anti-proliferation activity of shikonin on cancer cell lines by MTT assay. Moreover, in vivo anti-proliferation activity was tested in a mouse xenograft tumour model. RESULTS: Shikonin and its analogues inhibited recombinant human Cdc25 A, B, and C phosphatase with IC(50) values ranging from 2.14 ± 0.21 to 13.45 ± 1.45 μM irreversibly. The molecular modelling results showed that shikonin bound to the inhibitor binding pocket of Cdc25B with a favourable binding mode through hydrophobic interactions and hydrogen bonds. In addition, an accumulation of the tyrosine 15-phosphorylated form of CDK1 was induced by shikonin in a concentration-dependent manner in vitro and in vivo. We also confirmed that shikonin showed an anti-proliferation effect on three cancer cell lines with IC(50) values ranging from 6.15 ± 0.46 to 9.56 ± 1.03 μM. Furthermore, shikonin showed a promising anti-proliferation effect on a K562 mouse xenograph tumour model. CONCLUSION: In this study, we provide evidence for how shikonin induces cell cycle arrest and functions as a Cdc25s inhibitor. It shows an anti-proliferation effect both in vitro and in vivo by mediating Cdc25s. BioMed Central 2019-01-07 /pmc/articles/PMC6323793/ /pubmed/30616572 http://dx.doi.org/10.1186/s12885-018-5220-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Shoude
Gao, Qiang
Li, Wei
Zhu, Luwei
Shang, Qianhan
Feng, Shuo
Jia, Junmei
Jia, Qiangqiang
Shen, Shuo
Su, Zhanhai
Shikonin inhibits cancer cell cycling by targeting Cdc25s
title Shikonin inhibits cancer cell cycling by targeting Cdc25s
title_full Shikonin inhibits cancer cell cycling by targeting Cdc25s
title_fullStr Shikonin inhibits cancer cell cycling by targeting Cdc25s
title_full_unstemmed Shikonin inhibits cancer cell cycling by targeting Cdc25s
title_short Shikonin inhibits cancer cell cycling by targeting Cdc25s
title_sort shikonin inhibits cancer cell cycling by targeting cdc25s
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323793/
https://www.ncbi.nlm.nih.gov/pubmed/30616572
http://dx.doi.org/10.1186/s12885-018-5220-x
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