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Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids
The worldwide incidence of pulmonary carcinoids is increasing, but little is known about their molecular characteristics. Through machine learning and multi-omics factor analysis, we compare and contrast the genomic profiles of 116 pulmonary carcinoids (including 35 atypical), 75 large-cell neuroend...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702229/ https://www.ncbi.nlm.nih.gov/pubmed/31431620 http://dx.doi.org/10.1038/s41467-019-11276-9 |
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author | Alcala, N. Leblay, N. Gabriel, A. A. G. Mangiante, L. Hervas, D. Giffon, T. Sertier, A. S. Ferrari, A. Derks, J. Ghantous, A. Delhomme, T. M. Chabrier, A. Cuenin, C. Abedi-Ardekani, B. Boland, A. Olaso, R. Meyer, V. Altmuller, J. Le Calvez-Kelm, F. Durand, G. Voegele, C. Boyault, S. Moonen, L. Lemaitre, N. Lorimier, P. Toffart, A. C. Soltermann, A. Clement, J. H. Saenger, J. Field, J. K. Brevet, M. Blanc-Fournier, C. Galateau-Salle, F. Le Stang, N. Russell, P. A. Wright, G. Sozzi, G. Pastorino, U. Lacomme, S. Vignaud, J. M. Hofman, V. Hofman, P. Brustugun, O. T. Lund-Iversen, M. Thomas de Montpreville, V. Muscarella, L. A. Graziano, P. Popper, H. Stojsic, J. Deleuze, J. F. Herceg, Z. Viari, A. Nuernberg, P. Pelosi, G. Dingemans, A. M. C. Milione, M. Roz, L. Brcic, L. Volante, M. Papotti, M. G. Caux, C. Sandoval, J. Hernandez-Vargas, H. Brambilla, E. Speel, E. J. M. Girard, N. Lantuejoul, S. McKay, J. D. Foll, M. Fernandez-Cuesta, L. |
author_facet | Alcala, N. Leblay, N. Gabriel, A. A. G. Mangiante, L. Hervas, D. Giffon, T. Sertier, A. S. Ferrari, A. Derks, J. Ghantous, A. Delhomme, T. M. Chabrier, A. Cuenin, C. Abedi-Ardekani, B. Boland, A. Olaso, R. Meyer, V. Altmuller, J. Le Calvez-Kelm, F. Durand, G. Voegele, C. Boyault, S. Moonen, L. Lemaitre, N. Lorimier, P. Toffart, A. C. Soltermann, A. Clement, J. H. Saenger, J. Field, J. K. Brevet, M. Blanc-Fournier, C. Galateau-Salle, F. Le Stang, N. Russell, P. A. Wright, G. Sozzi, G. Pastorino, U. Lacomme, S. Vignaud, J. M. Hofman, V. Hofman, P. Brustugun, O. T. Lund-Iversen, M. Thomas de Montpreville, V. Muscarella, L. A. Graziano, P. Popper, H. Stojsic, J. Deleuze, J. F. Herceg, Z. Viari, A. Nuernberg, P. Pelosi, G. Dingemans, A. M. C. Milione, M. Roz, L. Brcic, L. Volante, M. Papotti, M. G. Caux, C. Sandoval, J. Hernandez-Vargas, H. Brambilla, E. Speel, E. J. M. Girard, N. Lantuejoul, S. McKay, J. D. Foll, M. Fernandez-Cuesta, L. |
author_sort | Alcala, N. |
collection | PubMed |
description | The worldwide incidence of pulmonary carcinoids is increasing, but little is known about their molecular characteristics. Through machine learning and multi-omics factor analysis, we compare and contrast the genomic profiles of 116 pulmonary carcinoids (including 35 atypical), 75 large-cell neuroendocrine carcinomas (LCNEC), and 66 small-cell lung cancers. Here we report that the integrative analyses on 257 lung neuroendocrine neoplasms stratify atypical carcinoids into two prognostic groups with a 10-year overall survival of 88% and 27%, respectively. We identify therapeutically relevant molecular groups of pulmonary carcinoids, suggesting DLL3 and the immune system as candidate therapeutic targets; we confirm the value of OTP expression levels for the prognosis and diagnosis of these diseases, and we unveil the group of supra-carcinoids. This group comprises samples with carcinoid-like morphology yet the molecular and clinical features of the deadly LCNEC, further supporting the previously proposed molecular link between the low- and high-grade lung neuroendocrine neoplasms. |
format | Online Article Text |
id | pubmed-6702229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67022292019-08-22 Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids Alcala, N. Leblay, N. Gabriel, A. A. G. Mangiante, L. Hervas, D. Giffon, T. Sertier, A. S. Ferrari, A. Derks, J. Ghantous, A. Delhomme, T. M. Chabrier, A. Cuenin, C. Abedi-Ardekani, B. Boland, A. Olaso, R. Meyer, V. Altmuller, J. Le Calvez-Kelm, F. Durand, G. Voegele, C. Boyault, S. Moonen, L. Lemaitre, N. Lorimier, P. Toffart, A. C. Soltermann, A. Clement, J. H. Saenger, J. Field, J. K. Brevet, M. Blanc-Fournier, C. Galateau-Salle, F. Le Stang, N. Russell, P. A. Wright, G. Sozzi, G. Pastorino, U. Lacomme, S. Vignaud, J. M. Hofman, V. Hofman, P. Brustugun, O. T. Lund-Iversen, M. Thomas de Montpreville, V. Muscarella, L. A. Graziano, P. Popper, H. Stojsic, J. Deleuze, J. F. Herceg, Z. Viari, A. Nuernberg, P. Pelosi, G. Dingemans, A. M. C. Milione, M. Roz, L. Brcic, L. Volante, M. Papotti, M. G. Caux, C. Sandoval, J. Hernandez-Vargas, H. Brambilla, E. Speel, E. J. M. Girard, N. Lantuejoul, S. McKay, J. D. Foll, M. Fernandez-Cuesta, L. Nat Commun Article The worldwide incidence of pulmonary carcinoids is increasing, but little is known about their molecular characteristics. Through machine learning and multi-omics factor analysis, we compare and contrast the genomic profiles of 116 pulmonary carcinoids (including 35 atypical), 75 large-cell neuroendocrine carcinomas (LCNEC), and 66 small-cell lung cancers. Here we report that the integrative analyses on 257 lung neuroendocrine neoplasms stratify atypical carcinoids into two prognostic groups with a 10-year overall survival of 88% and 27%, respectively. We identify therapeutically relevant molecular groups of pulmonary carcinoids, suggesting DLL3 and the immune system as candidate therapeutic targets; we confirm the value of OTP expression levels for the prognosis and diagnosis of these diseases, and we unveil the group of supra-carcinoids. This group comprises samples with carcinoid-like morphology yet the molecular and clinical features of the deadly LCNEC, further supporting the previously proposed molecular link between the low- and high-grade lung neuroendocrine neoplasms. Nature Publishing Group UK 2019-08-20 /pmc/articles/PMC6702229/ /pubmed/31431620 http://dx.doi.org/10.1038/s41467-019-11276-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Alcala, N. Leblay, N. Gabriel, A. A. G. Mangiante, L. Hervas, D. Giffon, T. Sertier, A. S. Ferrari, A. Derks, J. Ghantous, A. Delhomme, T. M. Chabrier, A. Cuenin, C. Abedi-Ardekani, B. Boland, A. Olaso, R. Meyer, V. Altmuller, J. Le Calvez-Kelm, F. Durand, G. Voegele, C. Boyault, S. Moonen, L. Lemaitre, N. Lorimier, P. Toffart, A. C. Soltermann, A. Clement, J. H. Saenger, J. Field, J. K. Brevet, M. Blanc-Fournier, C. Galateau-Salle, F. Le Stang, N. Russell, P. A. Wright, G. Sozzi, G. Pastorino, U. Lacomme, S. Vignaud, J. M. Hofman, V. Hofman, P. Brustugun, O. T. Lund-Iversen, M. Thomas de Montpreville, V. Muscarella, L. A. Graziano, P. Popper, H. Stojsic, J. Deleuze, J. F. Herceg, Z. Viari, A. Nuernberg, P. Pelosi, G. Dingemans, A. M. C. Milione, M. Roz, L. Brcic, L. Volante, M. Papotti, M. G. Caux, C. Sandoval, J. Hernandez-Vargas, H. Brambilla, E. Speel, E. J. M. Girard, N. Lantuejoul, S. McKay, J. D. Foll, M. Fernandez-Cuesta, L. Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title | Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title_full | Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title_fullStr | Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title_full_unstemmed | Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title_short | Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
title_sort | integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702229/ https://www.ncbi.nlm.nih.gov/pubmed/31431620 http://dx.doi.org/10.1038/s41467-019-11276-9 |
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