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Modeling the developmental origins of pediatric cancer to improve patient outcomes

In the treatment of children and adolescents with cancer, multimodal approaches combining surgery, chemotherapy and radiation can cure most patients, but may cause lifelong health problems in survivors. Current therapies only modestly reflect increased knowledge about the molecular mechanisms of the...

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Detalles Bibliográficos
Autor principal: Amatruda, James F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927656/
https://www.ncbi.nlm.nih.gov/pubmed/33619212
http://dx.doi.org/10.1242/dmm.048930
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author Amatruda, James F.
author_facet Amatruda, James F.
author_sort Amatruda, James F.
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description In the treatment of children and adolescents with cancer, multimodal approaches combining surgery, chemotherapy and radiation can cure most patients, but may cause lifelong health problems in survivors. Current therapies only modestly reflect increased knowledge about the molecular mechanisms of these cancers. Advances in next-generation sequencing have provided unprecedented cataloging of genetic aberrations in tumors, but understanding how these genetic changes drive cellular transformation, and how they can be effectively targeted, will require multidisciplinary collaboration and preclinical models that are truly representative of the in vivo environment. Here, I discuss some of the key challenges in pediatric cancer from my perspective as a physician-scientist, and touch on some promising new approaches that have the potential to transform our understanding of these diseases.
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spelling pubmed-79276562021-03-04 Modeling the developmental origins of pediatric cancer to improve patient outcomes Amatruda, James F. Dis Model Mech Perspective In the treatment of children and adolescents with cancer, multimodal approaches combining surgery, chemotherapy and radiation can cure most patients, but may cause lifelong health problems in survivors. Current therapies only modestly reflect increased knowledge about the molecular mechanisms of these cancers. Advances in next-generation sequencing have provided unprecedented cataloging of genetic aberrations in tumors, but understanding how these genetic changes drive cellular transformation, and how they can be effectively targeted, will require multidisciplinary collaboration and preclinical models that are truly representative of the in vivo environment. Here, I discuss some of the key challenges in pediatric cancer from my perspective as a physician-scientist, and touch on some promising new approaches that have the potential to transform our understanding of these diseases. The Company of Biologists Ltd 2021-02-22 /pmc/articles/PMC7927656/ /pubmed/33619212 http://dx.doi.org/10.1242/dmm.048930 Text en © 2021. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Perspective
Amatruda, James F.
Modeling the developmental origins of pediatric cancer to improve patient outcomes
title Modeling the developmental origins of pediatric cancer to improve patient outcomes
title_full Modeling the developmental origins of pediatric cancer to improve patient outcomes
title_fullStr Modeling the developmental origins of pediatric cancer to improve patient outcomes
title_full_unstemmed Modeling the developmental origins of pediatric cancer to improve patient outcomes
title_short Modeling the developmental origins of pediatric cancer to improve patient outcomes
title_sort modeling the developmental origins of pediatric cancer to improve patient outcomes
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927656/
https://www.ncbi.nlm.nih.gov/pubmed/33619212
http://dx.doi.org/10.1242/dmm.048930
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