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RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers

SIMPLE SUMMARY: High mammographic density (MD) is a significant risk factor for the development of breast cancer, as is inheritance of mutations in BRCA1 or BRCA2 tumour suppressor genes. High MD combined with BRCA1/2 gene mutations synergistically increases breast cancer risk, yet BRCA1/2 mutations...

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Autores principales: Reye, Gina, Huang, Xuan, Britt, Kara L., Meinert, Christoph, Blick, Tony, Xu, Yannan, Momot, Konstantin I., Lloyd, Thomas, Northey, Jason J., Thompson, Erik W., Hugo, Honor J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269117/
https://www.ncbi.nlm.nih.gov/pubmed/34209669
http://dx.doi.org/10.3390/cancers13133251
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author Reye, Gina
Huang, Xuan
Britt, Kara L.
Meinert, Christoph
Blick, Tony
Xu, Yannan
Momot, Konstantin I.
Lloyd, Thomas
Northey, Jason J.
Thompson, Erik W.
Hugo, Honor J.
author_facet Reye, Gina
Huang, Xuan
Britt, Kara L.
Meinert, Christoph
Blick, Tony
Xu, Yannan
Momot, Konstantin I.
Lloyd, Thomas
Northey, Jason J.
Thompson, Erik W.
Hugo, Honor J.
author_sort Reye, Gina
collection PubMed
description SIMPLE SUMMARY: High mammographic density (MD) is a significant risk factor for the development of breast cancer, as is inheritance of mutations in BRCA1 or BRCA2 tumour suppressor genes. High MD combined with BRCA1/2 gene mutations synergistically increases breast cancer risk, yet BRCA1/2 mutations alone or in combination do not increase MD or exacerbate the inherent tissue stiffness that high MD creates. The molecular basis for this additive effect therefore remains unclear. Our data indicate that the combinatory effect of high MD and BRCA mutations on breast cancer risk may be a product of repression of the tumour suppressor gene RASSF1A, in regions of increased tissue stiffness. ABSTRACT: High mammographic density (MD) increases breast cancer (BC) risk and creates a stiff tissue environment. BC risk is also increased in BRCA1/2 gene mutation carriers, which may be in part due to genetic disruption of the tumour suppressor gene Ras association domain family member 1 (RASSF1A), a gene that is also directly regulated by tissue stiffness. High MD combined with BRCA1/2 mutations further increase breast cancer risk, yet BRCA1/2 mutations alone or in combination do not increase MD. The molecular basis for this additive effect therefore remains unclear. We studied the interplay between MD, stiffness, and BRCA1/2 mutation status in human mammary tissue obtained after prophylactic mastectomy from women at risk of developing BC. Our results demonstrate that RASSF1A expression increased in MCF10DCIS.com cell cultures with matrix stiffness up until ranges corresponding with BiRADs 4 stiffnesses (~16 kPa), but decreased in higher stiffnesses approaching malignancy levels (>50 kPa). Similarly, higher RASSF1A protein was seen in these cells when co-cultivated with high MD tissue in murine biochambers. Conversely, local stiffness, as measured by collagen I versus III abundance, repressed RASSF1A protein expression in BRCA1, but not BRCA2 gene mutated tissues; regional density as measured radiographically repressed RASSF1A in both BRCA1/2 mutated tissues. The combinatory effect of high MD and BRCA mutations on breast cancer risk may be due to RASSF1A gene repression in regions of increased tissue stiffness.
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spelling pubmed-82691172021-07-10 RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers Reye, Gina Huang, Xuan Britt, Kara L. Meinert, Christoph Blick, Tony Xu, Yannan Momot, Konstantin I. Lloyd, Thomas Northey, Jason J. Thompson, Erik W. Hugo, Honor J. Cancers (Basel) Article SIMPLE SUMMARY: High mammographic density (MD) is a significant risk factor for the development of breast cancer, as is inheritance of mutations in BRCA1 or BRCA2 tumour suppressor genes. High MD combined with BRCA1/2 gene mutations synergistically increases breast cancer risk, yet BRCA1/2 mutations alone or in combination do not increase MD or exacerbate the inherent tissue stiffness that high MD creates. The molecular basis for this additive effect therefore remains unclear. Our data indicate that the combinatory effect of high MD and BRCA mutations on breast cancer risk may be a product of repression of the tumour suppressor gene RASSF1A, in regions of increased tissue stiffness. ABSTRACT: High mammographic density (MD) increases breast cancer (BC) risk and creates a stiff tissue environment. BC risk is also increased in BRCA1/2 gene mutation carriers, which may be in part due to genetic disruption of the tumour suppressor gene Ras association domain family member 1 (RASSF1A), a gene that is also directly regulated by tissue stiffness. High MD combined with BRCA1/2 mutations further increase breast cancer risk, yet BRCA1/2 mutations alone or in combination do not increase MD. The molecular basis for this additive effect therefore remains unclear. We studied the interplay between MD, stiffness, and BRCA1/2 mutation status in human mammary tissue obtained after prophylactic mastectomy from women at risk of developing BC. Our results demonstrate that RASSF1A expression increased in MCF10DCIS.com cell cultures with matrix stiffness up until ranges corresponding with BiRADs 4 stiffnesses (~16 kPa), but decreased in higher stiffnesses approaching malignancy levels (>50 kPa). Similarly, higher RASSF1A protein was seen in these cells when co-cultivated with high MD tissue in murine biochambers. Conversely, local stiffness, as measured by collagen I versus III abundance, repressed RASSF1A protein expression in BRCA1, but not BRCA2 gene mutated tissues; regional density as measured radiographically repressed RASSF1A in both BRCA1/2 mutated tissues. The combinatory effect of high MD and BRCA mutations on breast cancer risk may be due to RASSF1A gene repression in regions of increased tissue stiffness. MDPI 2021-06-29 /pmc/articles/PMC8269117/ /pubmed/34209669 http://dx.doi.org/10.3390/cancers13133251 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reye, Gina
Huang, Xuan
Britt, Kara L.
Meinert, Christoph
Blick, Tony
Xu, Yannan
Momot, Konstantin I.
Lloyd, Thomas
Northey, Jason J.
Thompson, Erik W.
Hugo, Honor J.
RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title_full RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title_fullStr RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title_full_unstemmed RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title_short RASSF1A Suppression as a Potential Regulator of Mechano-Pathobiology Associated with Mammographic Density in BRCA Mutation Carriers
title_sort rassf1a suppression as a potential regulator of mechano-pathobiology associated with mammographic density in brca mutation carriers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8269117/
https://www.ncbi.nlm.nih.gov/pubmed/34209669
http://dx.doi.org/10.3390/cancers13133251
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