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To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm

In the human embryo, the genetic program that orchestrates germ cell specification involves the activation of epigenetic and transcriptional mechanisms that make the germline a unique cell population continuously poised between germness and pluripotency. Germ cell tumors, neoplasias originating from...

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Detalles Bibliográficos
Autores principales: De Felici, Massimo, Klinger, Francesca Gioia, Campolo, Federica, Balistreri, Carmela Rita, Barchi, Marco, Dolci, Susanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199495/
https://www.ncbi.nlm.nih.gov/pubmed/34205983
http://dx.doi.org/10.3390/ijms22115982
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author De Felici, Massimo
Klinger, Francesca Gioia
Campolo, Federica
Balistreri, Carmela Rita
Barchi, Marco
Dolci, Susanna
author_facet De Felici, Massimo
Klinger, Francesca Gioia
Campolo, Federica
Balistreri, Carmela Rita
Barchi, Marco
Dolci, Susanna
author_sort De Felici, Massimo
collection PubMed
description In the human embryo, the genetic program that orchestrates germ cell specification involves the activation of epigenetic and transcriptional mechanisms that make the germline a unique cell population continuously poised between germness and pluripotency. Germ cell tumors, neoplasias originating from fetal or neonatal germ cells, maintain such dichotomy and can adopt either pluripotent features (embryonal carcinomas) or germness features (seminomas) with a wide range of phenotypes in between these histotypes. Here, we review the basic concepts of cell specification, migration and gonadal colonization of human primordial germ cells (hPGCs) highlighting the analogies of transcriptional/epigenetic programs between these two cell types.
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spelling pubmed-81994952021-06-14 To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm De Felici, Massimo Klinger, Francesca Gioia Campolo, Federica Balistreri, Carmela Rita Barchi, Marco Dolci, Susanna Int J Mol Sci Review In the human embryo, the genetic program that orchestrates germ cell specification involves the activation of epigenetic and transcriptional mechanisms that make the germline a unique cell population continuously poised between germness and pluripotency. Germ cell tumors, neoplasias originating from fetal or neonatal germ cells, maintain such dichotomy and can adopt either pluripotent features (embryonal carcinomas) or germness features (seminomas) with a wide range of phenotypes in between these histotypes. Here, we review the basic concepts of cell specification, migration and gonadal colonization of human primordial germ cells (hPGCs) highlighting the analogies of transcriptional/epigenetic programs between these two cell types. MDPI 2021-06-01 /pmc/articles/PMC8199495/ /pubmed/34205983 http://dx.doi.org/10.3390/ijms22115982 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
De Felici, Massimo
Klinger, Francesca Gioia
Campolo, Federica
Balistreri, Carmela Rita
Barchi, Marco
Dolci, Susanna
To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title_full To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title_fullStr To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title_full_unstemmed To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title_short To Be or Not to Be a Germ Cell: The Extragonadal Germ Cell Tumor Paradigm
title_sort to be or not to be a germ cell: the extragonadal germ cell tumor paradigm
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199495/
https://www.ncbi.nlm.nih.gov/pubmed/34205983
http://dx.doi.org/10.3390/ijms22115982
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