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Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway
BACKGROUND: Indirubin is the active component of Danggui Longhui Wan, a traditional Chinese medicine formulation. Due to its anti-inflammation and anti-tumor effects, indirubin has been widely used for the treatment of inflammation, cancer, and other chronic disease. Herein, we aimed to investigate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174913/ https://www.ncbi.nlm.nih.gov/pubmed/30323565 http://dx.doi.org/10.2147/DDDT.S174613 |
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author | Chen, Lihong Wang, Jinhua Wu, Jianbo Zheng, Qiaomei Hu, Jifen |
author_facet | Chen, Lihong Wang, Jinhua Wu, Jianbo Zheng, Qiaomei Hu, Jifen |
author_sort | Chen, Lihong |
collection | PubMed |
description | BACKGROUND: Indirubin is the active component of Danggui Longhui Wan, a traditional Chinese medicine formulation. Due to its anti-inflammation and anti-tumor effects, indirubin has been widely used for the treatment of inflammation, cancer, and other chronic disease. Herein, we aimed to investigate the role and mechanism of indirubin in human ovarian cancer cell proliferation. MATERIALS AND METHODS: The cell viability was determined by Cell Counting Kit-8 and colony formation assays by treatment with different dosages of indirubin over 72 hours. Apoptosis was examined by flow cytometry with fluorescein isothiocyanate Annexin V Apoptosis Detection Kit. Western blot assay was finally applied to analyze the expression of cancer-related STAT3 pathway and its downstream proteins. RESULTS: Indirubin was found to significantly inhibit cell viability and induce apoptosis in 2 human ovarian cancer cell lines. Mechanistic studies revealed that indirubin treatment led to reduced levels of phosphorylated-STAT3, thus repressing the downstream pro-survival proteins and elevating pro-apoptosis ones. CONCLUSION: Our study provided the evidence for anti-survival activity of indirubin by inhibiting cell viability and inducing apoptosis in human ovarian cancer cells, which involved impaired STAT3 signaling pathway. Our findings further support indirubin as a potential drug candidate against human ovarian cancer. |
format | Online Article Text |
id | pubmed-6174913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61749132018-10-15 Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway Chen, Lihong Wang, Jinhua Wu, Jianbo Zheng, Qiaomei Hu, Jifen Drug Des Devel Ther Original Research BACKGROUND: Indirubin is the active component of Danggui Longhui Wan, a traditional Chinese medicine formulation. Due to its anti-inflammation and anti-tumor effects, indirubin has been widely used for the treatment of inflammation, cancer, and other chronic disease. Herein, we aimed to investigate the role and mechanism of indirubin in human ovarian cancer cell proliferation. MATERIALS AND METHODS: The cell viability was determined by Cell Counting Kit-8 and colony formation assays by treatment with different dosages of indirubin over 72 hours. Apoptosis was examined by flow cytometry with fluorescein isothiocyanate Annexin V Apoptosis Detection Kit. Western blot assay was finally applied to analyze the expression of cancer-related STAT3 pathway and its downstream proteins. RESULTS: Indirubin was found to significantly inhibit cell viability and induce apoptosis in 2 human ovarian cancer cell lines. Mechanistic studies revealed that indirubin treatment led to reduced levels of phosphorylated-STAT3, thus repressing the downstream pro-survival proteins and elevating pro-apoptosis ones. CONCLUSION: Our study provided the evidence for anti-survival activity of indirubin by inhibiting cell viability and inducing apoptosis in human ovarian cancer cells, which involved impaired STAT3 signaling pathway. Our findings further support indirubin as a potential drug candidate against human ovarian cancer. Dove Medical Press 2018-10-04 /pmc/articles/PMC6174913/ /pubmed/30323565 http://dx.doi.org/10.2147/DDDT.S174613 Text en © 2018 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chen, Lihong Wang, Jinhua Wu, Jianbo Zheng, Qiaomei Hu, Jifen Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title | Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title_full | Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title_fullStr | Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title_full_unstemmed | Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title_short | Indirubin suppresses ovarian cancer cell viabilities through the STAT3 signaling pathway |
title_sort | indirubin suppresses ovarian cancer cell viabilities through the stat3 signaling pathway |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174913/ https://www.ncbi.nlm.nih.gov/pubmed/30323565 http://dx.doi.org/10.2147/DDDT.S174613 |
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