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Therapeutic Targeting of Integrin αvβ6 in Breast Cancer

BACKGROUND: Integrin αvβ6 promotes migration, invasion, and survival of cancer cells; however, the relevance and role of αvβ6 has yet to be elucidated in breast cancer. METHODS: Protein expression of integrin subunit beta6 (β6) was measured in breast cancers by immunohistochemistry (n > 2000) and...

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Autores principales: Moore, Kate M., Thomas, Gareth J., Duffy, Stephen W., Warwick, Jane, Gabe, Rhian, Chou, Patrick, Ellis, Ian O., Green, Andrew R., Haider, Syed, Brouilette, Kellie, Saha, Antonio, Vallath, Sabari, Bowen, Rebecca, Chelala, Claude, Eccles, Diana, Tapper, William J., Thompson, Alastair M., Quinlan, Phillip, Jordan, Lee, Gillett, Cheryl, Brentnall, Adam, Violette, Shelia, Weinreb, Paul H., Kendrew, Jane, Barry, Simon T., Hart, Ian R., Jones, J. Louise, Marshall, John F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151855/
https://www.ncbi.nlm.nih.gov/pubmed/24974129
http://dx.doi.org/10.1093/jnci/dju169
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author Moore, Kate M.
Thomas, Gareth J.
Duffy, Stephen W.
Warwick, Jane
Gabe, Rhian
Chou, Patrick
Ellis, Ian O.
Green, Andrew R.
Haider, Syed
Brouilette, Kellie
Saha, Antonio
Vallath, Sabari
Bowen, Rebecca
Chelala, Claude
Eccles, Diana
Tapper, William J.
Thompson, Alastair M.
Quinlan, Phillip
Jordan, Lee
Gillett, Cheryl
Brentnall, Adam
Violette, Shelia
Weinreb, Paul H.
Kendrew, Jane
Barry, Simon T.
Hart, Ian R.
Jones, J. Louise
Marshall, John F.
author_facet Moore, Kate M.
Thomas, Gareth J.
Duffy, Stephen W.
Warwick, Jane
Gabe, Rhian
Chou, Patrick
Ellis, Ian O.
Green, Andrew R.
Haider, Syed
Brouilette, Kellie
Saha, Antonio
Vallath, Sabari
Bowen, Rebecca
Chelala, Claude
Eccles, Diana
Tapper, William J.
Thompson, Alastair M.
Quinlan, Phillip
Jordan, Lee
Gillett, Cheryl
Brentnall, Adam
Violette, Shelia
Weinreb, Paul H.
Kendrew, Jane
Barry, Simon T.
Hart, Ian R.
Jones, J. Louise
Marshall, John F.
author_sort Moore, Kate M.
collection PubMed
description BACKGROUND: Integrin αvβ6 promotes migration, invasion, and survival of cancer cells; however, the relevance and role of αvβ6 has yet to be elucidated in breast cancer. METHODS: Protein expression of integrin subunit beta6 (β6) was measured in breast cancers by immunohistochemistry (n > 2000) and ITGB6 mRNA expression measured in the Molecular Taxonomy of Breast Cancer International Consortium dataset. Overall survival was assessed using Kaplan Meier curves, and bioinformatics statistical analyses were performed (Cox proportional hazards model, Wald test, and Chi-square test of association). Using antibody (264RAD) blockade and siRNA knockdown of β6 in breast cell lines, the role of αvβ6 in Human Epidermal Growth Factor Receptor 2 (HER2) biology (expression, proliferation, invasion, growth in vivo) was assessed by flow cytometry, MTT, Transwell invasion, proximity ligation assay, and xenografts (n ≥ 3), respectively. A student’s t-test was used for two variables; three-plus variables used one-way analysis of variance with Bonferroni’s Multiple Comparison Test. Xenograft growth was analyzed using linear mixed model analysis, followed by Wald testing and survival, analyzed using the Log-Rank test. All statistical tests were two sided. RESULTS: High expression of either the mRNA or protein for the integrin subunit β6 was associated with very poor survival (HR = 1.60, 95% CI = 1.19 to 2.15, P = .002) and increased metastases to distant sites. Co-expression of β6 and HER2 was associated with worse prognosis (HR = 1.97, 95% CI = 1.16 to 3.35, P = .01). Monotherapy with 264RAD or trastuzumab slowed growth of MCF-7/HER2-18 and BT-474 xenografts similarly (P < .001), but combining 264RAD with trastuzumab effectively stopped tumor growth, even in trastuzumab-resistant MCF-7/HER2-18 xenografts. CONCLUSIONS: Targeting αvβ6 with 264RAD alone or in combination with trastuzumab may provide a novel therapy for treating high-risk and trastuzumab-resistant breast cancer patients.
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spelling pubmed-41518552014-09-03 Therapeutic Targeting of Integrin αvβ6 in Breast Cancer Moore, Kate M. Thomas, Gareth J. Duffy, Stephen W. Warwick, Jane Gabe, Rhian Chou, Patrick Ellis, Ian O. Green, Andrew R. Haider, Syed Brouilette, Kellie Saha, Antonio Vallath, Sabari Bowen, Rebecca Chelala, Claude Eccles, Diana Tapper, William J. Thompson, Alastair M. Quinlan, Phillip Jordan, Lee Gillett, Cheryl Brentnall, Adam Violette, Shelia Weinreb, Paul H. Kendrew, Jane Barry, Simon T. Hart, Ian R. Jones, J. Louise Marshall, John F. J Natl Cancer Inst Article BACKGROUND: Integrin αvβ6 promotes migration, invasion, and survival of cancer cells; however, the relevance and role of αvβ6 has yet to be elucidated in breast cancer. METHODS: Protein expression of integrin subunit beta6 (β6) was measured in breast cancers by immunohistochemistry (n > 2000) and ITGB6 mRNA expression measured in the Molecular Taxonomy of Breast Cancer International Consortium dataset. Overall survival was assessed using Kaplan Meier curves, and bioinformatics statistical analyses were performed (Cox proportional hazards model, Wald test, and Chi-square test of association). Using antibody (264RAD) blockade and siRNA knockdown of β6 in breast cell lines, the role of αvβ6 in Human Epidermal Growth Factor Receptor 2 (HER2) biology (expression, proliferation, invasion, growth in vivo) was assessed by flow cytometry, MTT, Transwell invasion, proximity ligation assay, and xenografts (n ≥ 3), respectively. A student’s t-test was used for two variables; three-plus variables used one-way analysis of variance with Bonferroni’s Multiple Comparison Test. Xenograft growth was analyzed using linear mixed model analysis, followed by Wald testing and survival, analyzed using the Log-Rank test. All statistical tests were two sided. RESULTS: High expression of either the mRNA or protein for the integrin subunit β6 was associated with very poor survival (HR = 1.60, 95% CI = 1.19 to 2.15, P = .002) and increased metastases to distant sites. Co-expression of β6 and HER2 was associated with worse prognosis (HR = 1.97, 95% CI = 1.16 to 3.35, P = .01). Monotherapy with 264RAD or trastuzumab slowed growth of MCF-7/HER2-18 and BT-474 xenografts similarly (P < .001), but combining 264RAD with trastuzumab effectively stopped tumor growth, even in trastuzumab-resistant MCF-7/HER2-18 xenografts. CONCLUSIONS: Targeting αvβ6 with 264RAD alone or in combination with trastuzumab may provide a novel therapy for treating high-risk and trastuzumab-resistant breast cancer patients. Oxford University Press 2014-06-28 /pmc/articles/PMC4151855/ /pubmed/24974129 http://dx.doi.org/10.1093/jnci/dju169 Text en © The Author 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Moore, Kate M.
Thomas, Gareth J.
Duffy, Stephen W.
Warwick, Jane
Gabe, Rhian
Chou, Patrick
Ellis, Ian O.
Green, Andrew R.
Haider, Syed
Brouilette, Kellie
Saha, Antonio
Vallath, Sabari
Bowen, Rebecca
Chelala, Claude
Eccles, Diana
Tapper, William J.
Thompson, Alastair M.
Quinlan, Phillip
Jordan, Lee
Gillett, Cheryl
Brentnall, Adam
Violette, Shelia
Weinreb, Paul H.
Kendrew, Jane
Barry, Simon T.
Hart, Ian R.
Jones, J. Louise
Marshall, John F.
Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title_full Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title_fullStr Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title_full_unstemmed Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title_short Therapeutic Targeting of Integrin αvβ6 in Breast Cancer
title_sort therapeutic targeting of integrin αvβ6 in breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151855/
https://www.ncbi.nlm.nih.gov/pubmed/24974129
http://dx.doi.org/10.1093/jnci/dju169
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