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Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer

INTRODUCTION: Elafin is an elastase-specific inhibitor with increased transcription in normal mammary epithelial cells compared to mammary carcinoma cells. In this report, we test the hypothesis that inhibition of elastase, through induction of elafin, leads to inhibition of human breast cancer cell...

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Autores principales: Hunt, Kelly K, Wingate, Hannah, Yokota, Tomoya, Liu, Yanna, Mills, Gordon B, Zhang, Fan, Fang, Bingliang, Su, Chun-Hui, Zhang, Ming, Yi, Min, Keyomarsi, Khandan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672770/
https://www.ncbi.nlm.nih.gov/pubmed/23320734
http://dx.doi.org/10.1186/bcr3374
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author Hunt, Kelly K
Wingate, Hannah
Yokota, Tomoya
Liu, Yanna
Mills, Gordon B
Zhang, Fan
Fang, Bingliang
Su, Chun-Hui
Zhang, Ming
Yi, Min
Keyomarsi, Khandan
author_facet Hunt, Kelly K
Wingate, Hannah
Yokota, Tomoya
Liu, Yanna
Mills, Gordon B
Zhang, Fan
Fang, Bingliang
Su, Chun-Hui
Zhang, Ming
Yi, Min
Keyomarsi, Khandan
author_sort Hunt, Kelly K
collection PubMed
description INTRODUCTION: Elafin is an elastase-specific inhibitor with increased transcription in normal mammary epithelial cells compared to mammary carcinoma cells. In this report, we test the hypothesis that inhibition of elastase, through induction of elafin, leads to inhibition of human breast cancer cell viability and, therefore, predicts survival in breast cancer patients. METHODS: Panels of normal and immortalized breast epithelial cells, along with breast carcinoma cells, were used to examine the impact of adenoviral-mediated elafin expression or shRNA-mediated inhibition of elastase on the growth of cells and xenografts in nude mice. To determine the prognostic significance of decreased elafin in patients with invasive breast cancer, previously published gene array datasets were interrogated. RESULTS: Elafin expression had no effect on non-tumorigenic cells but resulted in marked inhibition of cell growth in breast cancer cell lines. Control-treated xenografts generated a tumor burden that necessitated sacrifice within one month of initial treatment, whereas xenograft-bearing mice treated with Ad-Elafin were alive at eight months with marked reduction in tumor growth. Elastase inhibition mimicked these results, showing decreased tumor cell growth in vitro and in vivo. Low expression of elafin gene correlated with significantly reduced time to relapse, and when combined with high expression of elastase gene was associated with decreased survival in breast cancer patients. CONCLUSION: Our data suggest that elafin plays a direct role in the suppression of tumors through inhibition of elastase and thus serves as a prognostic indicator for breast cancer patients.
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spelling pubmed-36727702013-06-06 Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer Hunt, Kelly K Wingate, Hannah Yokota, Tomoya Liu, Yanna Mills, Gordon B Zhang, Fan Fang, Bingliang Su, Chun-Hui Zhang, Ming Yi, Min Keyomarsi, Khandan Breast Cancer Res Research Article INTRODUCTION: Elafin is an elastase-specific inhibitor with increased transcription in normal mammary epithelial cells compared to mammary carcinoma cells. In this report, we test the hypothesis that inhibition of elastase, through induction of elafin, leads to inhibition of human breast cancer cell viability and, therefore, predicts survival in breast cancer patients. METHODS: Panels of normal and immortalized breast epithelial cells, along with breast carcinoma cells, were used to examine the impact of adenoviral-mediated elafin expression or shRNA-mediated inhibition of elastase on the growth of cells and xenografts in nude mice. To determine the prognostic significance of decreased elafin in patients with invasive breast cancer, previously published gene array datasets were interrogated. RESULTS: Elafin expression had no effect on non-tumorigenic cells but resulted in marked inhibition of cell growth in breast cancer cell lines. Control-treated xenografts generated a tumor burden that necessitated sacrifice within one month of initial treatment, whereas xenograft-bearing mice treated with Ad-Elafin were alive at eight months with marked reduction in tumor growth. Elastase inhibition mimicked these results, showing decreased tumor cell growth in vitro and in vivo. Low expression of elafin gene correlated with significantly reduced time to relapse, and when combined with high expression of elastase gene was associated with decreased survival in breast cancer patients. CONCLUSION: Our data suggest that elafin plays a direct role in the suppression of tumors through inhibition of elastase and thus serves as a prognostic indicator for breast cancer patients. BioMed Central 2013 2013-01-15 /pmc/articles/PMC3672770/ /pubmed/23320734 http://dx.doi.org/10.1186/bcr3374 Text en Copyright © 2013 Hunt et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hunt, Kelly K
Wingate, Hannah
Yokota, Tomoya
Liu, Yanna
Mills, Gordon B
Zhang, Fan
Fang, Bingliang
Su, Chun-Hui
Zhang, Ming
Yi, Min
Keyomarsi, Khandan
Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title_full Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title_fullStr Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title_full_unstemmed Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title_short Elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
title_sort elafin, an inhibitor of elastase, is a prognostic indicator in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672770/
https://www.ncbi.nlm.nih.gov/pubmed/23320734
http://dx.doi.org/10.1186/bcr3374
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