Cargando…
Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma
Pediatric tumors arise upon oncogenic transformation of stem/progenitor cells during embryonic development. Given this scenario, the existence of non-tumorigenic stem cells included within the aberrant tumoral niche, with a potential role in tumor biology, is an intriguing and unstudied possibility....
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685708/ https://www.ncbi.nlm.nih.gov/pubmed/29163787 http://dx.doi.org/10.18632/oncotarget.21128 |
_version_ | 1783278670038695936 |
---|---|
author | Linares-Clemente, Pedro Aguilar-Morante, Diana Rodríguez-Prieto, Ismael Ramírez, Gema de Torres, Carmen Santamaría, Vicente Pascual-Vaca, Diego Colmenero-Repiso, Ana Vega, Francisco M. Mora, Jaume Cabello, Rosa Márquez, Catalina Rivas, Eloy Pardal, Ricardo |
author_facet | Linares-Clemente, Pedro Aguilar-Morante, Diana Rodríguez-Prieto, Ismael Ramírez, Gema de Torres, Carmen Santamaría, Vicente Pascual-Vaca, Diego Colmenero-Repiso, Ana Vega, Francisco M. Mora, Jaume Cabello, Rosa Márquez, Catalina Rivas, Eloy Pardal, Ricardo |
author_sort | Linares-Clemente, Pedro |
collection | PubMed |
description | Pediatric tumors arise upon oncogenic transformation of stem/progenitor cells during embryonic development. Given this scenario, the existence of non-tumorigenic stem cells included within the aberrant tumoral niche, with a potential role in tumor biology, is an intriguing and unstudied possibility. Here, we describe the presence and function of non-tumorigenic neural crest-derived progenitor cells in aggressive neuroblastoma (NB) tumors. These cells differentiate into neural crest typical mesectodermal derivatives, giving rise to tumor stroma and promoting proliferation and tumor aggressiveness. Furthermore, an analysis of gene expression profiles in stage 4/M NB revealed a neural crest stem cell (NCSC) gene signature that was associated to stromal phenotype and high probability of relapse. Thus, this NCSC gene expression signature could be used in prognosis to improve stratification of stage 4/M NB tumors. Our results might facilitate the design of new therapies by targeting NCSCs and their contribution to tumor stroma. |
format | Online Article Text |
id | pubmed-5685708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56857082017-11-21 Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma Linares-Clemente, Pedro Aguilar-Morante, Diana Rodríguez-Prieto, Ismael Ramírez, Gema de Torres, Carmen Santamaría, Vicente Pascual-Vaca, Diego Colmenero-Repiso, Ana Vega, Francisco M. Mora, Jaume Cabello, Rosa Márquez, Catalina Rivas, Eloy Pardal, Ricardo Oncotarget Research Paper Pediatric tumors arise upon oncogenic transformation of stem/progenitor cells during embryonic development. Given this scenario, the existence of non-tumorigenic stem cells included within the aberrant tumoral niche, with a potential role in tumor biology, is an intriguing and unstudied possibility. Here, we describe the presence and function of non-tumorigenic neural crest-derived progenitor cells in aggressive neuroblastoma (NB) tumors. These cells differentiate into neural crest typical mesectodermal derivatives, giving rise to tumor stroma and promoting proliferation and tumor aggressiveness. Furthermore, an analysis of gene expression profiles in stage 4/M NB revealed a neural crest stem cell (NCSC) gene signature that was associated to stromal phenotype and high probability of relapse. Thus, this NCSC gene expression signature could be used in prognosis to improve stratification of stage 4/M NB tumors. Our results might facilitate the design of new therapies by targeting NCSCs and their contribution to tumor stroma. Impact Journals LLC 2017-09-21 /pmc/articles/PMC5685708/ /pubmed/29163787 http://dx.doi.org/10.18632/oncotarget.21128 Text en Copyright: © 2017 Linares-Clemente et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Linares-Clemente, Pedro Aguilar-Morante, Diana Rodríguez-Prieto, Ismael Ramírez, Gema de Torres, Carmen Santamaría, Vicente Pascual-Vaca, Diego Colmenero-Repiso, Ana Vega, Francisco M. Mora, Jaume Cabello, Rosa Márquez, Catalina Rivas, Eloy Pardal, Ricardo Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title | Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title_full | Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title_fullStr | Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title_full_unstemmed | Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title_short | Neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/M neuroblastoma |
title_sort | neural crest derived progenitor cells contribute to tumor stroma and aggressiveness in stage 4/m neuroblastoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5685708/ https://www.ncbi.nlm.nih.gov/pubmed/29163787 http://dx.doi.org/10.18632/oncotarget.21128 |
work_keys_str_mv | AT linaresclementepedro neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT aguilarmorantediana neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT rodriguezprietoismael neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT ramirezgema neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT detorrescarmen neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT santamariavicente neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT pascualvacadiego neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT colmenerorepisoana neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT vegafranciscom neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT morajaume neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT cabellorosa neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT marquezcatalina neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT rivaseloy neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma AT pardalricardo neuralcrestderivedprogenitorcellscontributetotumorstromaandaggressivenessinstage4mneuroblastoma |