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Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis
Cancer metastasis is refractory to most forms of chemotherapy. Conventional and alternative drugs, such as Chinese herbal remedies, have been developed to target metastatic cancer cells. In this study, we investigated the effects of PC-SPESII, an herbal formulation, on the migration, invasion, and m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708440/ https://www.ncbi.nlm.nih.gov/pubmed/23878609 http://dx.doi.org/10.1155/2013/894386 |
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author | Wang, Xiu-Feng Du, Jia Zhang, Tian-Ling Zhou, Qian-Mei Lu, Yi-Yu Zhang, Hui Su, Shi-Bing |
author_facet | Wang, Xiu-Feng Du, Jia Zhang, Tian-Ling Zhou, Qian-Mei Lu, Yi-Yu Zhang, Hui Su, Shi-Bing |
author_sort | Wang, Xiu-Feng |
collection | PubMed |
description | Cancer metastasis is refractory to most forms of chemotherapy. Conventional and alternative drugs, such as Chinese herbal remedies, have been developed to target metastatic cancer cells. In this study, we investigated the effects of PC-SPESII, an herbal formulation, on the migration, invasion, and metastasis of an experimental human breast cancer cell line in vivo and in vitro. PC-SPESII suppressed pulmonary metastasis and tumor growth of MDA-MB-231 human breast cancer xenografts without affecting body weight, liver function, and kidney function. PC-SPESII also inhibited MDA-MB-231 cell migration and invasion in vitro in a dose-dependent manner. Based on ELISA analysis, secretion of MMP-2 and MMP-9, proteins associated with extracellular matrix degradation, was reduced in response to PC-SPESII treatment. Western blot analysis of whole-cell extracts revealed that the levels of proteolytic proteins associated with matrix and base membrane degradation (MMP-2, MMP-9, and uPA) were decreased and the levels of their endogenous inhibitors (TIMP1 and TIMP2) were increased. Moreover, the p38MAPK and SAPK/JNK signaling pathway, which stimulates proteolytic enzymes and matrix degradation, was inhibited by PC-PSESII. Remarkably, cotreatment with PC-PSESII and p38MAPK or SAPK/JNK inhibitors magnified the antimetastatic phenotype. Our results indicate that PC-PSESII impairs human breast cancer metastasis by regulating proteolytic enzymes and matrix dynamics through the p38MAPK and SAPK/JNK pathway. |
format | Online Article Text |
id | pubmed-3708440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37084402013-07-22 Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis Wang, Xiu-Feng Du, Jia Zhang, Tian-Ling Zhou, Qian-Mei Lu, Yi-Yu Zhang, Hui Su, Shi-Bing Evid Based Complement Alternat Med Research Article Cancer metastasis is refractory to most forms of chemotherapy. Conventional and alternative drugs, such as Chinese herbal remedies, have been developed to target metastatic cancer cells. In this study, we investigated the effects of PC-SPESII, an herbal formulation, on the migration, invasion, and metastasis of an experimental human breast cancer cell line in vivo and in vitro. PC-SPESII suppressed pulmonary metastasis and tumor growth of MDA-MB-231 human breast cancer xenografts without affecting body weight, liver function, and kidney function. PC-SPESII also inhibited MDA-MB-231 cell migration and invasion in vitro in a dose-dependent manner. Based on ELISA analysis, secretion of MMP-2 and MMP-9, proteins associated with extracellular matrix degradation, was reduced in response to PC-SPESII treatment. Western blot analysis of whole-cell extracts revealed that the levels of proteolytic proteins associated with matrix and base membrane degradation (MMP-2, MMP-9, and uPA) were decreased and the levels of their endogenous inhibitors (TIMP1 and TIMP2) were increased. Moreover, the p38MAPK and SAPK/JNK signaling pathway, which stimulates proteolytic enzymes and matrix degradation, was inhibited by PC-PSESII. Remarkably, cotreatment with PC-PSESII and p38MAPK or SAPK/JNK inhibitors magnified the antimetastatic phenotype. Our results indicate that PC-PSESII impairs human breast cancer metastasis by regulating proteolytic enzymes and matrix dynamics through the p38MAPK and SAPK/JNK pathway. Hindawi Publishing Corporation 2013 2013-06-25 /pmc/articles/PMC3708440/ /pubmed/23878609 http://dx.doi.org/10.1155/2013/894386 Text en Copyright © 2013 Xiu-Feng Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Xiu-Feng Du, Jia Zhang, Tian-Ling Zhou, Qian-Mei Lu, Yi-Yu Zhang, Hui Su, Shi-Bing Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title | Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title_full | Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title_fullStr | Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title_full_unstemmed | Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title_short | Inhibitory Effects of PC-SPESII Herbal Extract on Human Breast Cancer Metastasis |
title_sort | inhibitory effects of pc-spesii herbal extract on human breast cancer metastasis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708440/ https://www.ncbi.nlm.nih.gov/pubmed/23878609 http://dx.doi.org/10.1155/2013/894386 |
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