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ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer

Triple negative breast cancer (TNBC), which comprises approximately 15% of all primary breast cancer diagnoses, lacks estrogen receptor alpha, progesterone receptor and human epidermal growth factor receptor 2 expression. However, we, and others, have demonstrated that approximately 30% of TNBCs exp...

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Autores principales: Reese, Jordan M., Bruinsma, Elizabeth S., Monroe, David G., Negron, Vivian, Suman, Vera J., Ingle, James N., Goetz, Matthew P., Hawse, John R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722501/
https://www.ncbi.nlm.nih.gov/pubmed/29228549
http://dx.doi.org/10.18632/oncotarget.21787
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author Reese, Jordan M.
Bruinsma, Elizabeth S.
Monroe, David G.
Negron, Vivian
Suman, Vera J.
Ingle, James N.
Goetz, Matthew P.
Hawse, John R.
author_facet Reese, Jordan M.
Bruinsma, Elizabeth S.
Monroe, David G.
Negron, Vivian
Suman, Vera J.
Ingle, James N.
Goetz, Matthew P.
Hawse, John R.
author_sort Reese, Jordan M.
collection PubMed
description Triple negative breast cancer (TNBC), which comprises approximately 15% of all primary breast cancer diagnoses, lacks estrogen receptor alpha, progesterone receptor and human epidermal growth factor receptor 2 expression. However, we, and others, have demonstrated that approximately 30% of TNBCs express estrogen receptor beta (ERβ), a nuclear hormone receptor and potential drug target. Treatment of ERβ expressing MDA-MB-231 cells with estrogen or the ERβ selective agonist, LY500307, was shown to result in suppression of cell proliferation. This inhibitory effect was due to blockade of cell cycle progression. In vivo, estrogen treatment significantly repressed the growth of ERβ expressing MDA-MB-231 cell line xenografts. Gene expression studies and ingenuity pathway analysis identified a network of ERβ down-regulated genes involved in cell cycle progression including CDK1, cyclin B and cyclin H. siRNA mediated knockdown or drug inhibition of CDK1 and CDK7 in TNBC cells resulted in substantial decreases in proliferation regardless of ERβ expression. These data suggest that the tumor suppressive effects of ERβ in TNBC result from inhibition of cell cycle progression, effects that are in part mediated by suppression of CDK1/7. Furthermore, these data indicate that blockade of CDK1/7 activity in TNBC may be of therapeutic benefit, an area of study that has yet to be explored.
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spelling pubmed-57225012017-12-10 ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer Reese, Jordan M. Bruinsma, Elizabeth S. Monroe, David G. Negron, Vivian Suman, Vera J. Ingle, James N. Goetz, Matthew P. Hawse, John R. Oncotarget Priority Research Paper Triple negative breast cancer (TNBC), which comprises approximately 15% of all primary breast cancer diagnoses, lacks estrogen receptor alpha, progesterone receptor and human epidermal growth factor receptor 2 expression. However, we, and others, have demonstrated that approximately 30% of TNBCs express estrogen receptor beta (ERβ), a nuclear hormone receptor and potential drug target. Treatment of ERβ expressing MDA-MB-231 cells with estrogen or the ERβ selective agonist, LY500307, was shown to result in suppression of cell proliferation. This inhibitory effect was due to blockade of cell cycle progression. In vivo, estrogen treatment significantly repressed the growth of ERβ expressing MDA-MB-231 cell line xenografts. Gene expression studies and ingenuity pathway analysis identified a network of ERβ down-regulated genes involved in cell cycle progression including CDK1, cyclin B and cyclin H. siRNA mediated knockdown or drug inhibition of CDK1 and CDK7 in TNBC cells resulted in substantial decreases in proliferation regardless of ERβ expression. These data suggest that the tumor suppressive effects of ERβ in TNBC result from inhibition of cell cycle progression, effects that are in part mediated by suppression of CDK1/7. Furthermore, these data indicate that blockade of CDK1/7 activity in TNBC may be of therapeutic benefit, an area of study that has yet to be explored. Impact Journals LLC 2017-10-11 /pmc/articles/PMC5722501/ /pubmed/29228549 http://dx.doi.org/10.18632/oncotarget.21787 Text en Copyright: © 2017 Reese et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Priority Research Paper
Reese, Jordan M.
Bruinsma, Elizabeth S.
Monroe, David G.
Negron, Vivian
Suman, Vera J.
Ingle, James N.
Goetz, Matthew P.
Hawse, John R.
ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title_full ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title_fullStr ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title_full_unstemmed ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title_short ERβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
title_sort erβ inhibits cyclin dependent kinases 1 and 7 in triple negative breast cancer
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722501/
https://www.ncbi.nlm.nih.gov/pubmed/29228549
http://dx.doi.org/10.18632/oncotarget.21787
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