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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...

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Autores principales: Maire, Virginie, Mahmood, Faisal, Rigaill, Guillem, Ye, Mengliang, Brisson, Amélie, Némati, Fariba, Gentien, David, Tucker, Gordon C., Roman‐Roman, Sergio, Dubois, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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.
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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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