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NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients

BACKGROUND: The presence of disseminated tumor cells (DTCs) in bone marrow (BM) is an independent prognostic factor in early breast cancer but does not uniformly predict outcome. Tumor cells can persist in a quiescent state over time, but clinical studies of markers predicting the awakening potentia...

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Autores principales: Borgen, Elin, Rypdal, Maria C., Sosa, Maria Soledad, Renolen, Anne, Schlichting, Ellen, Lønning, Per E., Synnestvedt, Marit, Aguirre-Ghiso, Julio A., Naume, Bjørn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190561/
https://www.ncbi.nlm.nih.gov/pubmed/30322396
http://dx.doi.org/10.1186/s13058-018-1049-0
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author Borgen, Elin
Rypdal, Maria C.
Sosa, Maria Soledad
Renolen, Anne
Schlichting, Ellen
Lønning, Per E.
Synnestvedt, Marit
Aguirre-Ghiso, Julio A.
Naume, Bjørn
author_facet Borgen, Elin
Rypdal, Maria C.
Sosa, Maria Soledad
Renolen, Anne
Schlichting, Ellen
Lønning, Per E.
Synnestvedt, Marit
Aguirre-Ghiso, Julio A.
Naume, Bjørn
author_sort Borgen, Elin
collection PubMed
description BACKGROUND: The presence of disseminated tumor cells (DTCs) in bone marrow (BM) is an independent prognostic factor in early breast cancer but does not uniformly predict outcome. Tumor cells can persist in a quiescent state over time, but clinical studies of markers predicting the awakening potential of DTCs are lacking. Recently, experiments have shown that NR2F1 (COUP-TF1) plays a key role in dormancy signaling. METHODS: We analyzed the NR2F1 expression in DTCs by double immunofluorescence (DIF) staining of extra cytospins prepared from 114 BM samples from 86 selected DTC-positive breast cancer patients. Samples collected at two or more time points were available for 24 patients. Fifteen samples were also analyzed for the proliferation marker Ki67. RESULTS: Of the patients with detectable DTCs by DIF, 27% had ≥ 50% NR2F1(high) DTCs, chosen a priori as the cut-off for “dormant profile” classification. All patients with systemic relapse within 12 months after BM aspiration carried ≤ 1% NR2F1(high) DTCs, including patients who transitioned from having NR2F1(high)-expressing DTCs in previous BM samples. Of the patients with serial samples, half of those with no relapse at follow-up had ≥ 50% NR2F1(high) DTCs in the last BM aspiration analyzed. Among the 18 relapse-free patients at the time of the last DTC-positive BM aspiration with no subsequent BM analysis performed, distant disease-free intervals were favorable for patients carrying ≥ 50% NR2F1(high) DTCs compared with those with predominantly NR2F1(low) DTCs (p = 0.007, log-rank). No survival difference was observed by classification according to Ki67-expressing DTCs (p = 0.520). CONCLUSIONS: Our study translates findings from basic biological analysis of DTC dormancy to the clinical situation and supports further clinical studies of NR2F1 as a marker of dormancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-018-1049-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-61905612018-10-23 NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients Borgen, Elin Rypdal, Maria C. Sosa, Maria Soledad Renolen, Anne Schlichting, Ellen Lønning, Per E. Synnestvedt, Marit Aguirre-Ghiso, Julio A. Naume, Bjørn Breast Cancer Res Short Report BACKGROUND: The presence of disseminated tumor cells (DTCs) in bone marrow (BM) is an independent prognostic factor in early breast cancer but does not uniformly predict outcome. Tumor cells can persist in a quiescent state over time, but clinical studies of markers predicting the awakening potential of DTCs are lacking. Recently, experiments have shown that NR2F1 (COUP-TF1) plays a key role in dormancy signaling. METHODS: We analyzed the NR2F1 expression in DTCs by double immunofluorescence (DIF) staining of extra cytospins prepared from 114 BM samples from 86 selected DTC-positive breast cancer patients. Samples collected at two or more time points were available for 24 patients. Fifteen samples were also analyzed for the proliferation marker Ki67. RESULTS: Of the patients with detectable DTCs by DIF, 27% had ≥ 50% NR2F1(high) DTCs, chosen a priori as the cut-off for “dormant profile” classification. All patients with systemic relapse within 12 months after BM aspiration carried ≤ 1% NR2F1(high) DTCs, including patients who transitioned from having NR2F1(high)-expressing DTCs in previous BM samples. Of the patients with serial samples, half of those with no relapse at follow-up had ≥ 50% NR2F1(high) DTCs in the last BM aspiration analyzed. Among the 18 relapse-free patients at the time of the last DTC-positive BM aspiration with no subsequent BM analysis performed, distant disease-free intervals were favorable for patients carrying ≥ 50% NR2F1(high) DTCs compared with those with predominantly NR2F1(low) DTCs (p = 0.007, log-rank). No survival difference was observed by classification according to Ki67-expressing DTCs (p = 0.520). CONCLUSIONS: Our study translates findings from basic biological analysis of DTC dormancy to the clinical situation and supports further clinical studies of NR2F1 as a marker of dormancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-018-1049-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-16 2018 /pmc/articles/PMC6190561/ /pubmed/30322396 http://dx.doi.org/10.1186/s13058-018-1049-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Borgen, Elin
Rypdal, Maria C.
Sosa, Maria Soledad
Renolen, Anne
Schlichting, Ellen
Lønning, Per E.
Synnestvedt, Marit
Aguirre-Ghiso, Julio A.
Naume, Bjørn
NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title_full NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title_fullStr NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title_full_unstemmed NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title_short NR2F1 stratifies dormant disseminated tumor cells in breast cancer patients
title_sort nr2f1 stratifies dormant disseminated tumor cells in breast cancer patients
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6190561/
https://www.ncbi.nlm.nih.gov/pubmed/30322396
http://dx.doi.org/10.1186/s13058-018-1049-0
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