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LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors
Triple‐negative breast cancer (TNBC) is the breast cancer subtype with the worst prognosis. New treatments improving the survival of TNBC patients are, therefore, urgently required. We performed a transcriptome microarray analysis to identify new treatment targets for TNBC. We found that low‐density...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346259/ https://www.ncbi.nlm.nih.gov/pubmed/30575334 http://dx.doi.org/10.1002/cam4.1923 |
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author | Maire, Virginie Mahmood, Faisal Rigaill, Guillem Ye, Mengliang Brisson, Amélie Némati, Fariba Gentien, David Tucker, Gordon C. Roman‐Roman, Sergio Dubois, Thierry |
author_facet | Maire, Virginie Mahmood, Faisal Rigaill, Guillem Ye, Mengliang Brisson, Amélie Némati, Fariba Gentien, David Tucker, Gordon C. Roman‐Roman, Sergio Dubois, Thierry |
author_sort | Maire, Virginie |
collection | PubMed |
description | Triple‐negative breast cancer (TNBC) is the breast cancer subtype with the worst prognosis. New treatments improving the survival of TNBC patients are, therefore, urgently required. We performed a transcriptome microarray analysis to identify new treatment targets for TNBC. We found that low‐density lipoprotein receptor‐related protein 8 (LRP8) was more strongly expressed in estrogen receptor‐negative breast tumors, including TNBCs and those overexpressing HER2, than in luminal breast tumors and normal breast tissues. LRP8 depletion decreased cell proliferation more efficiently in estrogen receptor‐negative breast cancer cell lines: TNBC and HER2 overexpressing cell lines. We next focused on TNBC cells for which targeted therapies are not available. LRP8 depletion induced an arrest of the cell cycle progression in G1 phase and programmed cell death. We also found that LRP8 is required for anchorage‐independent growth in vitro, and that its depletion in vivo slowed tumor growth in a xenograft model. Our findings suggest that new approaches targeting LRP8 may constitute promising treatments for hormone‐negative breast cancers, those overexpressing HER2 and TNBCs. |
format | Online Article Text |
id | pubmed-6346259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63462592019-01-29 LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors Maire, Virginie Mahmood, Faisal Rigaill, Guillem Ye, Mengliang Brisson, Amélie Némati, Fariba Gentien, David Tucker, Gordon C. Roman‐Roman, Sergio Dubois, Thierry Cancer Med Cancer Biology Triple‐negative breast cancer (TNBC) is the breast cancer subtype with the worst prognosis. New treatments improving the survival of TNBC patients are, therefore, urgently required. We performed a transcriptome microarray analysis to identify new treatment targets for TNBC. We found that low‐density lipoprotein receptor‐related protein 8 (LRP8) was more strongly expressed in estrogen receptor‐negative breast tumors, including TNBCs and those overexpressing HER2, than in luminal breast tumors and normal breast tissues. LRP8 depletion decreased cell proliferation more efficiently in estrogen receptor‐negative breast cancer cell lines: TNBC and HER2 overexpressing cell lines. We next focused on TNBC cells for which targeted therapies are not available. LRP8 depletion induced an arrest of the cell cycle progression in G1 phase and programmed cell death. We also found that LRP8 is required for anchorage‐independent growth in vitro, and that its depletion in vivo slowed tumor growth in a xenograft model. Our findings suggest that new approaches targeting LRP8 may constitute promising treatments for hormone‐negative breast cancers, those overexpressing HER2 and TNBCs. John Wiley and Sons Inc. 2018-12-21 /pmc/articles/PMC6346259/ /pubmed/30575334 http://dx.doi.org/10.1002/cam4.1923 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Maire, Virginie Mahmood, Faisal Rigaill, Guillem Ye, Mengliang Brisson, Amélie Némati, Fariba Gentien, David Tucker, Gordon C. Roman‐Roman, Sergio Dubois, Thierry LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title | LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title_full | LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title_fullStr | LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title_full_unstemmed | LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title_short | LRP8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
title_sort | lrp8 is overexpressed in estrogen‐negative breast cancers and a potential target for these tumors |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346259/ https://www.ncbi.nlm.nih.gov/pubmed/30575334 http://dx.doi.org/10.1002/cam4.1923 |
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