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Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer
Diallyl disulfide (DADS), a volatile component of garlic oil, has various biological properties, including antioxidant, antiangiogenic and anticancer effects. The present study aimed to explore novel targets of DADS that may slow or stop the progression of breast cancer. First, xenograft tumor model...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920483/ https://www.ncbi.nlm.nih.gov/pubmed/29725473 http://dx.doi.org/10.3892/ol.2018.8299 |
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author | Xiong, Ting Liu, Xiao-Wang Huang, Xue-Long Xu, Xiong-Feng Xie, Wei-Quan Zhang, Su-Jun Tu, Jian |
author_facet | Xiong, Ting Liu, Xiao-Wang Huang, Xue-Long Xu, Xiong-Feng Xie, Wei-Quan Zhang, Su-Jun Tu, Jian |
author_sort | Xiong, Ting |
collection | PubMed |
description | Diallyl disulfide (DADS), a volatile component of garlic oil, has various biological properties, including antioxidant, antiangiogenic and anticancer effects. The present study aimed to explore novel targets of DADS that may slow or stop the progression of breast cancer. First, xenograft tumor models were created by subcutaneously injecting MCF-7 and MDA-MB-231 breast cancer cells into nude mice. Subsequently, western blot analysis was performed to investigate the expression of tristetraprolin (TTP), urokinase-type plasminogen activator (uPA) and matrix metalloproteinase-9 (MMP-9) in the xenograft tumors, and cell cultures. Tablet cloning, Transwell and wound healing assays revealed that DADS treatment significantly inhibited the proliferation, invasion and migration of breast cancer cells. In addition, DADS treatment led to significant downregulation of uPA and MMP-9 protein expression, but significantly upregulated TTP expression in vivo and in vitro. Knocking down TTP expression using small interfering RNA reversed the aforementioned effects of DADS, which suggests TTP is a key target of DADS in inhibiting the progression of breast cancer. |
format | Online Article Text |
id | pubmed-5920483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-59204832018-05-03 Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer Xiong, Ting Liu, Xiao-Wang Huang, Xue-Long Xu, Xiong-Feng Xie, Wei-Quan Zhang, Su-Jun Tu, Jian Oncol Lett Articles Diallyl disulfide (DADS), a volatile component of garlic oil, has various biological properties, including antioxidant, antiangiogenic and anticancer effects. The present study aimed to explore novel targets of DADS that may slow or stop the progression of breast cancer. First, xenograft tumor models were created by subcutaneously injecting MCF-7 and MDA-MB-231 breast cancer cells into nude mice. Subsequently, western blot analysis was performed to investigate the expression of tristetraprolin (TTP), urokinase-type plasminogen activator (uPA) and matrix metalloproteinase-9 (MMP-9) in the xenograft tumors, and cell cultures. Tablet cloning, Transwell and wound healing assays revealed that DADS treatment significantly inhibited the proliferation, invasion and migration of breast cancer cells. In addition, DADS treatment led to significant downregulation of uPA and MMP-9 protein expression, but significantly upregulated TTP expression in vivo and in vitro. Knocking down TTP expression using small interfering RNA reversed the aforementioned effects of DADS, which suggests TTP is a key target of DADS in inhibiting the progression of breast cancer. D.A. Spandidos 2018-05 2018-03-20 /pmc/articles/PMC5920483/ /pubmed/29725473 http://dx.doi.org/10.3892/ol.2018.8299 Text en Copyright: © Xiong 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 Xiong, Ting Liu, Xiao-Wang Huang, Xue-Long Xu, Xiong-Feng Xie, Wei-Quan Zhang, Su-Jun Tu, Jian Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title | Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title_full | Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title_fullStr | Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title_full_unstemmed | Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title_short | Tristetraprolin: A novel target of diallyl disulfide that inhibits the progression of breast cancer |
title_sort | tristetraprolin: a novel target of diallyl disulfide that inhibits the progression of breast cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920483/ https://www.ncbi.nlm.nih.gov/pubmed/29725473 http://dx.doi.org/10.3892/ol.2018.8299 |
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