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Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis
Puerarin 6″-O-xyloside (PRX) is a major compound found in the root of the Pueraria lobata (Willd.) Ohwi. The present study aimed to investigate the antitumor activity of PRX against colon cancer and examine its possible mechanism. In the present study, the anti-proliferative effects of PRX against c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176249/ https://www.ncbi.nlm.nih.gov/pubmed/30344709 http://dx.doi.org/10.3892/ol.2018.9364 |
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author | Zhang, Xiao-Lan Wang, Bin-Bin Mo, Jian-Shu |
author_facet | Zhang, Xiao-Lan Wang, Bin-Bin Mo, Jian-Shu |
author_sort | Zhang, Xiao-Lan |
collection | PubMed |
description | Puerarin 6″-O-xyloside (PRX) is a major compound found in the root of the Pueraria lobata (Willd.) Ohwi. The present study aimed to investigate the antitumor activity of PRX against colon cancer and examine its possible mechanism. In the present study, the anti-proliferative effects of PRX against colon cell lines (SW480, LoVo and HCT-116) were evaluated using a Cell Counting Kit-8 assay, and the half maximal inhibitory concentration values of the SW480, LoVo and HCT-11 cells were 37.114, 49.213 and 43.022 µg/ml, respectively. Furthermore, the apoptosis of SW480 cells was detected using flow cytometry with Annexin V-fluorescein isothiocyanate/propidium iodide staining. Subsequently, western blot analysis was performed to examine the expression of proteins associated with apoptosis, invasion and metastasis of tumors. The results showed that PRX possessed antitumor activity against colon cancer cell lines in a dose-dependent and time-dependent manner. In addition, PRX significantly upregulated the expression levels of cleaved (c)-caspase-3, c-caspase-9, B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein and phosphorylated c-Jun terminal kinase, and downregulated the expression levels of Bcl-2, matrix metalloproteinase (MMP)-3, MMP-9 and vascular endothelial growth factor (P<0.01). Therefore, the present study demonstrated the PRX exerted antitumor activity against colon cancer cell lines and that the anticancer mechanisms of PRX may be associated with the induction of mitochondria-mediated intrinsic apoptosis, and inhibition of tumor invasion and metastasis. The present study provides a scientific basis for the clinical use of PRX for the treatment of colon cancer. |
format | Online Article Text |
id | pubmed-6176249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-61762492018-10-21 Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis Zhang, Xiao-Lan Wang, Bin-Bin Mo, Jian-Shu Oncol Lett Articles Puerarin 6″-O-xyloside (PRX) is a major compound found in the root of the Pueraria lobata (Willd.) Ohwi. The present study aimed to investigate the antitumor activity of PRX against colon cancer and examine its possible mechanism. In the present study, the anti-proliferative effects of PRX against colon cell lines (SW480, LoVo and HCT-116) were evaluated using a Cell Counting Kit-8 assay, and the half maximal inhibitory concentration values of the SW480, LoVo and HCT-11 cells were 37.114, 49.213 and 43.022 µg/ml, respectively. Furthermore, the apoptosis of SW480 cells was detected using flow cytometry with Annexin V-fluorescein isothiocyanate/propidium iodide staining. Subsequently, western blot analysis was performed to examine the expression of proteins associated with apoptosis, invasion and metastasis of tumors. The results showed that PRX possessed antitumor activity against colon cancer cell lines in a dose-dependent and time-dependent manner. In addition, PRX significantly upregulated the expression levels of cleaved (c)-caspase-3, c-caspase-9, B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein and phosphorylated c-Jun terminal kinase, and downregulated the expression levels of Bcl-2, matrix metalloproteinase (MMP)-3, MMP-9 and vascular endothelial growth factor (P<0.01). Therefore, the present study demonstrated the PRX exerted antitumor activity against colon cancer cell lines and that the anticancer mechanisms of PRX may be associated with the induction of mitochondria-mediated intrinsic apoptosis, and inhibition of tumor invasion and metastasis. The present study provides a scientific basis for the clinical use of PRX for the treatment of colon cancer. D.A. Spandidos 2018-11 2018-08-24 /pmc/articles/PMC6176249/ /pubmed/30344709 http://dx.doi.org/10.3892/ol.2018.9364 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, Xiao-Lan Wang, Bin-Bin Mo, Jian-Shu Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title | Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title_full | Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title_fullStr | Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title_full_unstemmed | Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title_short | Puerarin 6″-O-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
title_sort | puerarin 6″-o-xyloside possesses significant antitumor activities on colon cancer through inducing apoptosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176249/ https://www.ncbi.nlm.nih.gov/pubmed/30344709 http://dx.doi.org/10.3892/ol.2018.9364 |
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