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Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression

Protosappanin B (PSB) is a key active component of Lignum Sappan extract. Although the antiproliferative effects of Lignum Sappan extract have been demonstrated in various cancer cells, relatively little is known about the effects of PSB on tumor progression. The aim of this study was to explore the...

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Autores principales: Zheng, Xue-Cong, Shi, Ze-Sheng, Qiu, Cheng-Zhi, Hong, Zhong-Shi, Wang, Chun-Xiao, Zhuang, Hai-Bin, Chen, Zhi-Chuan, Pan, Jian-Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727080/
https://www.ncbi.nlm.nih.gov/pubmed/33289438
http://dx.doi.org/10.1177/1534735420972477
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author Zheng, Xue-Cong
Shi, Ze-Sheng
Qiu, Cheng-Zhi
Hong, Zhong-Shi
Wang, Chun-Xiao
Zhuang, Hai-Bin
Chen, Zhi-Chuan
Pan, Jian-Peng
author_facet Zheng, Xue-Cong
Shi, Ze-Sheng
Qiu, Cheng-Zhi
Hong, Zhong-Shi
Wang, Chun-Xiao
Zhuang, Hai-Bin
Chen, Zhi-Chuan
Pan, Jian-Peng
author_sort Zheng, Xue-Cong
collection PubMed
description Protosappanin B (PSB) is a key active component of Lignum Sappan extract. Although the antiproliferative effects of Lignum Sappan extract have been demonstrated in various cancer cells, relatively little is known about the effects of PSB on tumor progression. The aim of this study was to explore the anti-tumor effects of PSB on human colon cancer cells by regulation of intracellular signaling pathways and Golgi phosphoprotein 3 (GOLPH3) expression in vitro and in vivo. Our results showed that PSB effectively inhibited the viability and migration of SW620 cells and induced apoptosis, but had poor effect on HCT116 cells. Furthermore, PSB significantly reduced the expression of p-AKT, p-p70S6K, β-catenin, and p-ERK1/2 proteins in SW620 cells, and this effect was reversed by the corresponding signaling pathway agonists. Interestingly, PSB could also suppress GOLPH3 expression of SW620 cells in a concentration-dependent manner, but SW620 cells transfected with lentiviral vectors overexpressing GOLPH3 can effectively resist the cytotoxic activity of PSB in vitro. The xenograft experiment of SW620 cells with LV-GOLPH3 confirmed that PSB distinctly inhibited the tumor growth via suppressing GOLPH3 expression. Collectively, these findings clarified a new anti-cancer mechanism of PSB through inhibition of GOLPH3 expression and intracellular signaling pathways in colon cancer cells. PSB may be a potential new drug for colon cancer.
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spelling pubmed-77270802020-12-18 Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression Zheng, Xue-Cong Shi, Ze-Sheng Qiu, Cheng-Zhi Hong, Zhong-Shi Wang, Chun-Xiao Zhuang, Hai-Bin Chen, Zhi-Chuan Pan, Jian-Peng Integr Cancer Ther Research Article Protosappanin B (PSB) is a key active component of Lignum Sappan extract. Although the antiproliferative effects of Lignum Sappan extract have been demonstrated in various cancer cells, relatively little is known about the effects of PSB on tumor progression. The aim of this study was to explore the anti-tumor effects of PSB on human colon cancer cells by regulation of intracellular signaling pathways and Golgi phosphoprotein 3 (GOLPH3) expression in vitro and in vivo. Our results showed that PSB effectively inhibited the viability and migration of SW620 cells and induced apoptosis, but had poor effect on HCT116 cells. Furthermore, PSB significantly reduced the expression of p-AKT, p-p70S6K, β-catenin, and p-ERK1/2 proteins in SW620 cells, and this effect was reversed by the corresponding signaling pathway agonists. Interestingly, PSB could also suppress GOLPH3 expression of SW620 cells in a concentration-dependent manner, but SW620 cells transfected with lentiviral vectors overexpressing GOLPH3 can effectively resist the cytotoxic activity of PSB in vitro. The xenograft experiment of SW620 cells with LV-GOLPH3 confirmed that PSB distinctly inhibited the tumor growth via suppressing GOLPH3 expression. Collectively, these findings clarified a new anti-cancer mechanism of PSB through inhibition of GOLPH3 expression and intracellular signaling pathways in colon cancer cells. PSB may be a potential new drug for colon cancer. SAGE Publications 2020-12-08 /pmc/articles/PMC7727080/ /pubmed/33289438 http://dx.doi.org/10.1177/1534735420972477 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Article
Zheng, Xue-Cong
Shi, Ze-Sheng
Qiu, Cheng-Zhi
Hong, Zhong-Shi
Wang, Chun-Xiao
Zhuang, Hai-Bin
Chen, Zhi-Chuan
Pan, Jian-Peng
Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title_full Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title_fullStr Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title_full_unstemmed Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title_short Protosappanin B Exerts Anti-tumor Effects on Colon Cancer Cells via Inhibiting GOLPH3 Expression
title_sort protosappanin b exerts anti-tumor effects on colon cancer cells via inhibiting golph3 expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727080/
https://www.ncbi.nlm.nih.gov/pubmed/33289438
http://dx.doi.org/10.1177/1534735420972477
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