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Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer

Gastric cancer is the third leading cause of cancer-associated deaths worldwide. Research into the underlying mechanisms of gastric cancer is essential for the development of novel therapeutic agents to improve the prognoses of patients with gastric cancer. Tanshinone IIA (Tan IIA) is the pure extra...

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Autores principales: Zhang, Yongjun, Guo, Shuguang, Fang, Jian, Peng, Bojian, Zhang, Yuan, Cao, Tiansheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125958/
https://www.ncbi.nlm.nih.gov/pubmed/30214513
http://dx.doi.org/10.3892/etm.2018.6562
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author Zhang, Yongjun
Guo, Shuguang
Fang, Jian
Peng, Bojian
Zhang, Yuan
Cao, Tiansheng
author_facet Zhang, Yongjun
Guo, Shuguang
Fang, Jian
Peng, Bojian
Zhang, Yuan
Cao, Tiansheng
author_sort Zhang, Yongjun
collection PubMed
description Gastric cancer is the third leading cause of cancer-associated deaths worldwide. Research into the underlying mechanisms of gastric cancer is essential for the development of novel therapeutic agents to improve the prognoses of patients with gastric cancer. Tanshinone IIA (Tan IIA) is the pure extract of Danshen root (Salvia miltiorrhiza) and has been report to inhibit the proliferation of gastric cancer cells; however, the intrinsic underlying mechanisms remain unclear. The aim of the present study was to investigate whether Tan IIA has a direct anti-cancer effect in gastric cancer cells and determine the underlying mechanisms responsible. The results revealed that Tan IIA effectively inhibits proliferation in three human gastric cancer cell lines (SNU-638, MKN1 and AGS) in a time- and dose-dependent manner. Furthermore, Tan IIA treatment induced an increase in apoptosis, B-cell lymphoma (Bcl-2)-associated protein X expression and cleaved caspase-3 levels, as well as a decrease in Bcl-2 expression. Treatment with Tan IIA inhibited Furthermore, treatment with Tan IIA significantly inhibited the phosphorylation of signal transducer and activator of transcription 3 (STAT3), which may be responsible for the changes in apoptosis gene expression. However, overexpression of STAT3 significantly ameliorated the Tan IIA-induced suppression of cell growth and apoptosis. A nude mouse xenograft model was constructed and the results revealed that intraperitoneal Tan IIA treatment for 28 days significantly inhibited tumor growth and STAT3 activation. The results of the present study suggest that Tan IIA exerts potent anti-cancer activity in gastric cancer cells and this effect is mediated by the downregulation of STAT3 activation.
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spelling pubmed-61259582018-09-13 Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer Zhang, Yongjun Guo, Shuguang Fang, Jian Peng, Bojian Zhang, Yuan Cao, Tiansheng Exp Ther Med Articles Gastric cancer is the third leading cause of cancer-associated deaths worldwide. Research into the underlying mechanisms of gastric cancer is essential for the development of novel therapeutic agents to improve the prognoses of patients with gastric cancer. Tanshinone IIA (Tan IIA) is the pure extract of Danshen root (Salvia miltiorrhiza) and has been report to inhibit the proliferation of gastric cancer cells; however, the intrinsic underlying mechanisms remain unclear. The aim of the present study was to investigate whether Tan IIA has a direct anti-cancer effect in gastric cancer cells and determine the underlying mechanisms responsible. The results revealed that Tan IIA effectively inhibits proliferation in three human gastric cancer cell lines (SNU-638, MKN1 and AGS) in a time- and dose-dependent manner. Furthermore, Tan IIA treatment induced an increase in apoptosis, B-cell lymphoma (Bcl-2)-associated protein X expression and cleaved caspase-3 levels, as well as a decrease in Bcl-2 expression. Treatment with Tan IIA inhibited Furthermore, treatment with Tan IIA significantly inhibited the phosphorylation of signal transducer and activator of transcription 3 (STAT3), which may be responsible for the changes in apoptosis gene expression. However, overexpression of STAT3 significantly ameliorated the Tan IIA-induced suppression of cell growth and apoptosis. A nude mouse xenograft model was constructed and the results revealed that intraperitoneal Tan IIA treatment for 28 days significantly inhibited tumor growth and STAT3 activation. The results of the present study suggest that Tan IIA exerts potent anti-cancer activity in gastric cancer cells and this effect is mediated by the downregulation of STAT3 activation. D.A. Spandidos 2018-10 2018-08-02 /pmc/articles/PMC6125958/ /pubmed/30214513 http://dx.doi.org/10.3892/etm.2018.6562 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhang, Yongjun
Guo, Shuguang
Fang, Jian
Peng, Bojian
Zhang, Yuan
Cao, Tiansheng
Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title_full Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title_fullStr Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title_full_unstemmed Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title_short Tanshinone IIA inhibits cell proliferation and tumor growth by downregulating STAT3 in human gastric cancer
title_sort tanshinone iia inhibits cell proliferation and tumor growth by downregulating stat3 in human gastric cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125958/
https://www.ncbi.nlm.nih.gov/pubmed/30214513
http://dx.doi.org/10.3892/etm.2018.6562
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