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Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib

BACKGROUND: Breast cancer stem cells (BCSCs) have been recognized as playing a major role in various aspects of breast cancer biology. To identify specific biomarkers of BCSCs, we have performed comparative proteomics of BCSC-enriched and mature cancer cell populations from the human breast cancer c...

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Autores principales: Gilabert, Marine, Launay, Simon, Ginestier, Christophe, Bertucci, François, Audebert, Stéphane, Pophillat, Mathieu, Toiron, Yves, Baudelet, Emilie, Finetti, Pascal, Noguchi, Tetsuro, Sobol, Hagay, Birnbaum, Daniel, Borg, Jean-Paul, Charafe-Jauffret, Emmanuelle, Gonçalves, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140711/
https://www.ncbi.nlm.nih.gov/pubmed/25144364
http://dx.doi.org/10.1371/journal.pone.0104302
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author Gilabert, Marine
Launay, Simon
Ginestier, Christophe
Bertucci, François
Audebert, Stéphane
Pophillat, Mathieu
Toiron, Yves
Baudelet, Emilie
Finetti, Pascal
Noguchi, Tetsuro
Sobol, Hagay
Birnbaum, Daniel
Borg, Jean-Paul
Charafe-Jauffret, Emmanuelle
Gonçalves, Anthony
author_facet Gilabert, Marine
Launay, Simon
Ginestier, Christophe
Bertucci, François
Audebert, Stéphane
Pophillat, Mathieu
Toiron, Yves
Baudelet, Emilie
Finetti, Pascal
Noguchi, Tetsuro
Sobol, Hagay
Birnbaum, Daniel
Borg, Jean-Paul
Charafe-Jauffret, Emmanuelle
Gonçalves, Anthony
author_sort Gilabert, Marine
collection PubMed
description BACKGROUND: Breast cancer stem cells (BCSCs) have been recognized as playing a major role in various aspects of breast cancer biology. To identify specific biomarkers of BCSCs, we have performed comparative proteomics of BCSC-enriched and mature cancer cell populations from the human breast cancer cell line (BCL), BrCA-MZ-01. METHODS: ALDEFLUOR assay was used to sort BCSC-enriched (ALDH+) and mature cancer (ALDH−) cell populations. Total proteins were extracted from both fractions and subjected to 2-Dimensional Difference In-Gel Electrophoresis (2-D DIGE). Differentially-expressed spots were excised and proteins were gel-extracted, digested and identified using MALDI-TOF MS. RESULTS: 2-D DIGE identified poly(ADP-ribose) polymerase 1 (PARP1) as overexpressed in ALDH+ cells from BrCA-MZ-01. This observation was confirmed by western blot and extended to four additional human BCLs. ALDH+ cells from BRCA1-mutated HCC1937, which had the highest level of PARP1 overexpression, displayed resistance to olaparib, a specific PARP1 inhibitor. CONCLUSION: An unbiased proteomic approach identified PARP1 as upregulated in ALDH+, BCSC-enriched cells from various human BCLs, which may contribute to clinical resistance to PARP inhibitors.
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spelling pubmed-41407112014-08-25 Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib Gilabert, Marine Launay, Simon Ginestier, Christophe Bertucci, François Audebert, Stéphane Pophillat, Mathieu Toiron, Yves Baudelet, Emilie Finetti, Pascal Noguchi, Tetsuro Sobol, Hagay Birnbaum, Daniel Borg, Jean-Paul Charafe-Jauffret, Emmanuelle Gonçalves, Anthony PLoS One Research Article BACKGROUND: Breast cancer stem cells (BCSCs) have been recognized as playing a major role in various aspects of breast cancer biology. To identify specific biomarkers of BCSCs, we have performed comparative proteomics of BCSC-enriched and mature cancer cell populations from the human breast cancer cell line (BCL), BrCA-MZ-01. METHODS: ALDEFLUOR assay was used to sort BCSC-enriched (ALDH+) and mature cancer (ALDH−) cell populations. Total proteins were extracted from both fractions and subjected to 2-Dimensional Difference In-Gel Electrophoresis (2-D DIGE). Differentially-expressed spots were excised and proteins were gel-extracted, digested and identified using MALDI-TOF MS. RESULTS: 2-D DIGE identified poly(ADP-ribose) polymerase 1 (PARP1) as overexpressed in ALDH+ cells from BrCA-MZ-01. This observation was confirmed by western blot and extended to four additional human BCLs. ALDH+ cells from BRCA1-mutated HCC1937, which had the highest level of PARP1 overexpression, displayed resistance to olaparib, a specific PARP1 inhibitor. CONCLUSION: An unbiased proteomic approach identified PARP1 as upregulated in ALDH+, BCSC-enriched cells from various human BCLs, which may contribute to clinical resistance to PARP inhibitors. Public Library of Science 2014-08-21 /pmc/articles/PMC4140711/ /pubmed/25144364 http://dx.doi.org/10.1371/journal.pone.0104302 Text en © 2014 Gilabert et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gilabert, Marine
Launay, Simon
Ginestier, Christophe
Bertucci, François
Audebert, Stéphane
Pophillat, Mathieu
Toiron, Yves
Baudelet, Emilie
Finetti, Pascal
Noguchi, Tetsuro
Sobol, Hagay
Birnbaum, Daniel
Borg, Jean-Paul
Charafe-Jauffret, Emmanuelle
Gonçalves, Anthony
Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title_full Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title_fullStr Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title_full_unstemmed Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title_short Poly(ADP-Ribose) Polymerase 1 (PARP1) Overexpression in Human Breast Cancer Stem Cells and Resistance to Olaparib
title_sort poly(adp-ribose) polymerase 1 (parp1) overexpression in human breast cancer stem cells and resistance to olaparib
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140711/
https://www.ncbi.nlm.nih.gov/pubmed/25144364
http://dx.doi.org/10.1371/journal.pone.0104302
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