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Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration
BACKGROUND: Exopolysaccharides with structural diversity have shown wide applications in biomaterial, food, and pharmaceutical industries. Herein, we isolated an endophytic strain, 14‐DS‐1, from the traditional medicinal plant Codonopsis pilosula to elucidate the characteristics and anti‐cancer acti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928371/ https://www.ncbi.nlm.nih.gov/pubmed/29577649 http://dx.doi.org/10.1111/1759-7714.12630 |
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author | Chen, Min Li, Yuanyuan Liu, Zhu Qu, Yajun Zhang, Huajie Li, Dengwen Zhou, Jun Xie, Songbo Liu, Min |
author_facet | Chen, Min Li, Yuanyuan Liu, Zhu Qu, Yajun Zhang, Huajie Li, Dengwen Zhou, Jun Xie, Songbo Liu, Min |
author_sort | Chen, Min |
collection | PubMed |
description | BACKGROUND: Exopolysaccharides with structural diversity have shown wide applications in biomaterial, food, and pharmaceutical industries. Herein, we isolated an endophytic strain, 14‐DS‐1, from the traditional medicinal plant Codonopsis pilosula to elucidate the characteristics and anti‐cancer activities of purified exopolysaccharides. METHODS: HPLC and GC‐MS were conducted to purify and characterize the exopolysaccharides isolated from 14‐DS‐1. Quantitative RT‐PCR, cell migration assays, immunofluorescence staining, and flow cytometry analysis were conducted to investighate the biological activity of DSPS. RESULTS: We demonstrated that exopolysaccharides isolated from 14‐DS‐1 (DSPS), which were predominately composed of six monosaccharides, showed anti‐cancer activities. Biological activity analysis revealed that exposure to DSPS induced macrophage activation and polarization by promoting the production of TNF‐α and nitric oxide. Further analysis revealed that DSPS treatment promoted macrophage infiltration, whereas cancer cell migration was suppressed. In addition, DSPS exposure led to S‐phase arrest and apoptosis in cancer cells. Immunofluorescence staining revealed that treatment with DSPS resulted in defects in spindle orientation and positioning. CONCLUSION: These findings thus suggest that DSPS may have promising potential in cancer therapy. |
format | Online Article Text |
id | pubmed-5928371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59283712018-05-07 Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration Chen, Min Li, Yuanyuan Liu, Zhu Qu, Yajun Zhang, Huajie Li, Dengwen Zhou, Jun Xie, Songbo Liu, Min Thorac Cancer Original Articles BACKGROUND: Exopolysaccharides with structural diversity have shown wide applications in biomaterial, food, and pharmaceutical industries. Herein, we isolated an endophytic strain, 14‐DS‐1, from the traditional medicinal plant Codonopsis pilosula to elucidate the characteristics and anti‐cancer activities of purified exopolysaccharides. METHODS: HPLC and GC‐MS were conducted to purify and characterize the exopolysaccharides isolated from 14‐DS‐1. Quantitative RT‐PCR, cell migration assays, immunofluorescence staining, and flow cytometry analysis were conducted to investighate the biological activity of DSPS. RESULTS: We demonstrated that exopolysaccharides isolated from 14‐DS‐1 (DSPS), which were predominately composed of six monosaccharides, showed anti‐cancer activities. Biological activity analysis revealed that exposure to DSPS induced macrophage activation and polarization by promoting the production of TNF‐α and nitric oxide. Further analysis revealed that DSPS treatment promoted macrophage infiltration, whereas cancer cell migration was suppressed. In addition, DSPS exposure led to S‐phase arrest and apoptosis in cancer cells. Immunofluorescence staining revealed that treatment with DSPS resulted in defects in spindle orientation and positioning. CONCLUSION: These findings thus suggest that DSPS may have promising potential in cancer therapy. John Wiley & Sons Australia, Ltd 2018-03-25 2018-05 /pmc/articles/PMC5928371/ /pubmed/29577649 http://dx.doi.org/10.1111/1759-7714.12630 Text en © 2018 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Chen, Min Li, Yuanyuan Liu, Zhu Qu, Yajun Zhang, Huajie Li, Dengwen Zhou, Jun Xie, Songbo Liu, Min Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title | Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title_full | Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title_fullStr | Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title_full_unstemmed | Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title_short | Exopolysaccharides from a Codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
title_sort | exopolysaccharides from a codonopsis pilosula endophyte activate macrophages and inhibit cancer cell proliferation and migration |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928371/ https://www.ncbi.nlm.nih.gov/pubmed/29577649 http://dx.doi.org/10.1111/1759-7714.12630 |
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