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BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer

We have recently demonstrated that a natural dietary supplement BreastDefend (BD), which contains extracts from medicinal mushrooms (Coriolus versicolor, Ganoderma lucidum, Phellinus linteus), medicinal herbs (Scutellaria barbata, Astragalus membranaceus, Curcuma longa), and purified biologically ac...

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Autores principales: JIANG, JIAHUA, THYAGARAJAN-SAHU, ANITA, LOGANATHAN, JAGADISH, ELIAZ, ISAAC, TERRY, COLIN, SANDUSKY, GEORGE E., SLIVA, DANIEL
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583511/
https://www.ncbi.nlm.nih.gov/pubmed/22842551
http://dx.doi.org/10.3892/or.2012.1936
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author JIANG, JIAHUA
THYAGARAJAN-SAHU, ANITA
LOGANATHAN, JAGADISH
ELIAZ, ISAAC
TERRY, COLIN
SANDUSKY, GEORGE E.
SLIVA, DANIEL
author_facet JIANG, JIAHUA
THYAGARAJAN-SAHU, ANITA
LOGANATHAN, JAGADISH
ELIAZ, ISAAC
TERRY, COLIN
SANDUSKY, GEORGE E.
SLIVA, DANIEL
author_sort JIANG, JIAHUA
collection PubMed
description We have recently demonstrated that a natural dietary supplement BreastDefend (BD), which contains extracts from medicinal mushrooms (Coriolus versicolor, Ganoderma lucidum, Phellinus linteus), medicinal herbs (Scutellaria barbata, Astragalus membranaceus, Curcuma longa), and purified biologically active nutritional compounds (diindolylmethane and quercetin), inhibits proliferation and metastatic behavior of MDA-MB-231 invasive human breast cancer cells in vitro. In the present study, we evaluated whether BD suppresses growth and breast-to lung cancer metastasis in an orthotopic model of human breast cancer cells implanted in mice. Oral application of BD (100 mg/kg of body weight for 4 weeks) by intragastric gavage did not affect body weight or activity of liver enzymes and did not show any sign of toxicity in liver, spleen, kidney, lung and heart tissues in mice. Moreover, BD significantly decreased the change in tumor volume over time compared to the control group (p=0.002). BD treatment also markedly decreased the incidence of breast-to-lung cancer metastasis from 67% (control) to 20% (BD) (p<0.05) and the number of metastases from 2.8 (0.0, 48.0) in the control group to 0.0 (0.0, 14.2) in the BD treatment group (p<0.05). Finally, anti-metastatic activity of BD in vivo was further confirmed by the downregulation of expression of PLAU (urokinase plasminogen activator, uPA) and CXCR4 (C-X-C chemokine receptor-4) genes in breast tumors. In conclusion, BD may be considered as a biological therapeutic agent against invasive breast cancers.
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spelling pubmed-35835112013-02-28 BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer JIANG, JIAHUA THYAGARAJAN-SAHU, ANITA LOGANATHAN, JAGADISH ELIAZ, ISAAC TERRY, COLIN SANDUSKY, GEORGE E. SLIVA, DANIEL Oncol Rep Articles We have recently demonstrated that a natural dietary supplement BreastDefend (BD), which contains extracts from medicinal mushrooms (Coriolus versicolor, Ganoderma lucidum, Phellinus linteus), medicinal herbs (Scutellaria barbata, Astragalus membranaceus, Curcuma longa), and purified biologically active nutritional compounds (diindolylmethane and quercetin), inhibits proliferation and metastatic behavior of MDA-MB-231 invasive human breast cancer cells in vitro. In the present study, we evaluated whether BD suppresses growth and breast-to lung cancer metastasis in an orthotopic model of human breast cancer cells implanted in mice. Oral application of BD (100 mg/kg of body weight for 4 weeks) by intragastric gavage did not affect body weight or activity of liver enzymes and did not show any sign of toxicity in liver, spleen, kidney, lung and heart tissues in mice. Moreover, BD significantly decreased the change in tumor volume over time compared to the control group (p=0.002). BD treatment also markedly decreased the incidence of breast-to-lung cancer metastasis from 67% (control) to 20% (BD) (p<0.05) and the number of metastases from 2.8 (0.0, 48.0) in the control group to 0.0 (0.0, 14.2) in the BD treatment group (p<0.05). Finally, anti-metastatic activity of BD in vivo was further confirmed by the downregulation of expression of PLAU (urokinase plasminogen activator, uPA) and CXCR4 (C-X-C chemokine receptor-4) genes in breast tumors. In conclusion, BD may be considered as a biological therapeutic agent against invasive breast cancers. D.A. Spandidos 2012-10 2012-07-26 /pmc/articles/PMC3583511/ /pubmed/22842551 http://dx.doi.org/10.3892/or.2012.1936 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
JIANG, JIAHUA
THYAGARAJAN-SAHU, ANITA
LOGANATHAN, JAGADISH
ELIAZ, ISAAC
TERRY, COLIN
SANDUSKY, GEORGE E.
SLIVA, DANIEL
BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title_full BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title_fullStr BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title_full_unstemmed BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title_short BreastDefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
title_sort breastdefend™ prevents breast-to-lung cancer metastases in an orthotopic animal model of triple-negative human breast cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583511/
https://www.ncbi.nlm.nih.gov/pubmed/22842551
http://dx.doi.org/10.3892/or.2012.1936
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