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Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells

The roots of Codonopsis cordifolioidea (classified as campanulaceae cordifolioidea), locally known as Tsoong, have been used as a tonic food. The major components isolated from Tsoong have been demonstrated to present anti-human immunodeficiency virus-1 activities and cytotoxicity against various tu...

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Autores principales: Luan, Yun-Peng, Li, Qi-Feng, Wu, Shi-Guo, Mao, De-Chang, Deng, Yan-Yun, Chen, Rong-Wang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802150/
https://www.ncbi.nlm.nih.gov/pubmed/29286105
http://dx.doi.org/10.3892/mmr.2017.8328
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author Luan, Yun-Peng
Li, Qi-Feng
Wu, Shi-Guo
Mao, De-Chang
Deng, Yan-Yun
Chen, Rong-Wang
author_facet Luan, Yun-Peng
Li, Qi-Feng
Wu, Shi-Guo
Mao, De-Chang
Deng, Yan-Yun
Chen, Rong-Wang
author_sort Luan, Yun-Peng
collection PubMed
description The roots of Codonopsis cordifolioidea (classified as campanulaceae cordifolioidea), locally known as Tsoong, have been used as a tonic food. The major components isolated from Tsoong have been demonstrated to present anti-human immunodeficiency virus-1 activities and cytotoxicity against various tumor cell lines. However, the possible effects of the novel compound isolated from Tsoong, cordifoliketones A, on pancreatic ductal adenocarcinoma (PDAC) cells, are still unknown. In the present study, cordifoliketones A extractions were prepared from Tsoong, and the possible effects on PDAC cell growth, apoptosis, migration and invasion in vitro and in vivo were exlored. The cytotoxicity assay, apoptosis assay, western blotting, migration and invasion assay, and a PDAC cell (AsPC-1, BxPC-3 and PANC-1) xenograft mice model were employed. The results demonstrated that treatment with cordifoliketones A: i) inhibited proliferation and promoted apoptosis of PDAC cells; ii) significantly induced apoptosis and altered expression of apoptosis-associated proteins in a dose-dependent manner; iii) suppressed migration and invasion of PDAC cells in a dose-dependent manner; and iv) restrained the growth of PDAC neoplasm in nude mice. Furthermore, cordifoliketones A demonstrated non-cytotoxic activity in a panel of normal human cells, including hTERT-HPNE, 293, hepatocyte HL-7702 and HL-1 cells. Therefore, these data indicated that cordifoliketones A may be a potential candidate compound for the prevention of PDAC cell proliferation and metastasis, presumably by induction apoptosis and inhibiting viability, invasion and migration of PDAC cells.
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spelling pubmed-58021502018-02-26 Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells Luan, Yun-Peng Li, Qi-Feng Wu, Shi-Guo Mao, De-Chang Deng, Yan-Yun Chen, Rong-Wang Mol Med Rep Articles The roots of Codonopsis cordifolioidea (classified as campanulaceae cordifolioidea), locally known as Tsoong, have been used as a tonic food. The major components isolated from Tsoong have been demonstrated to present anti-human immunodeficiency virus-1 activities and cytotoxicity against various tumor cell lines. However, the possible effects of the novel compound isolated from Tsoong, cordifoliketones A, on pancreatic ductal adenocarcinoma (PDAC) cells, are still unknown. In the present study, cordifoliketones A extractions were prepared from Tsoong, and the possible effects on PDAC cell growth, apoptosis, migration and invasion in vitro and in vivo were exlored. The cytotoxicity assay, apoptosis assay, western blotting, migration and invasion assay, and a PDAC cell (AsPC-1, BxPC-3 and PANC-1) xenograft mice model were employed. The results demonstrated that treatment with cordifoliketones A: i) inhibited proliferation and promoted apoptosis of PDAC cells; ii) significantly induced apoptosis and altered expression of apoptosis-associated proteins in a dose-dependent manner; iii) suppressed migration and invasion of PDAC cells in a dose-dependent manner; and iv) restrained the growth of PDAC neoplasm in nude mice. Furthermore, cordifoliketones A demonstrated non-cytotoxic activity in a panel of normal human cells, including hTERT-HPNE, 293, hepatocyte HL-7702 and HL-1 cells. Therefore, these data indicated that cordifoliketones A may be a potential candidate compound for the prevention of PDAC cell proliferation and metastasis, presumably by induction apoptosis and inhibiting viability, invasion and migration of PDAC cells. D.A. Spandidos 2018-03 2017-12-20 /pmc/articles/PMC5802150/ /pubmed/29286105 http://dx.doi.org/10.3892/mmr.2017.8328 Text en Copyright: © Luan 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
Luan, Yun-Peng
Li, Qi-Feng
Wu, Shi-Guo
Mao, De-Chang
Deng, Yan-Yun
Chen, Rong-Wang
Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title_full Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title_fullStr Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title_full_unstemmed Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title_short Tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
title_sort tsoong induces apoptosis and inhibits proliferation, migration and invasion of pancreatic ductal adenocarcinoma cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802150/
https://www.ncbi.nlm.nih.gov/pubmed/29286105
http://dx.doi.org/10.3892/mmr.2017.8328
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