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Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification
Pancreatic ductal adenocarcinoma (PDAC), the most common form of pancreatic cancer, is an extremely lethal disease due to late diagnosis, aggressiveness and lack of effective therapies. Considering its intrinsic heterogeneity, patient stratification models based on transcriptomic and genomic signatu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767410/ https://www.ncbi.nlm.nih.gov/pubmed/33371431 http://dx.doi.org/10.3390/jcm9124128 |
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author | Espiau-Romera, Pilar Courtois, Sarah Parejo-Alonso, Beatriz Sancho, Patricia |
author_facet | Espiau-Romera, Pilar Courtois, Sarah Parejo-Alonso, Beatriz Sancho, Patricia |
author_sort | Espiau-Romera, Pilar |
collection | PubMed |
description | Pancreatic ductal adenocarcinoma (PDAC), the most common form of pancreatic cancer, is an extremely lethal disease due to late diagnosis, aggressiveness and lack of effective therapies. Considering its intrinsic heterogeneity, patient stratification models based on transcriptomic and genomic signatures, with partially overlapping subgroups, have been established. Besides molecular alterations, PDAC tumours show a strong desmoplastic response, resulting in profound metabolic reprogramming involving increased glucose and amino acid consumption, as well as lipid scavenging and biosynthesis. Interestingly, recent works have also revealed the existence of metabolic subtypes with differential prognosis within PDAC, which correlated to defined molecular subclasses in patients: lipogenic subtype correlated with a classical/progenitor signature, while glycolytic tumours associated with the highly aggressive basal/squamous profile. Bioinformatic analyses have demonstrated that the representative genes of each metabolic subtype are up-regulated in PDAC samples and predict patient survival. This suggests a relationship between the genetic signature, metabolic profile, and aggressiveness of the tumour. Considering all this, defining metabolic subtypes represents a clear opportunity for patient stratification considering tumour functional behaviour independently of their mutational background. |
format | Online Article Text |
id | pubmed-7767410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77674102020-12-28 Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification Espiau-Romera, Pilar Courtois, Sarah Parejo-Alonso, Beatriz Sancho, Patricia J Clin Med Review Pancreatic ductal adenocarcinoma (PDAC), the most common form of pancreatic cancer, is an extremely lethal disease due to late diagnosis, aggressiveness and lack of effective therapies. Considering its intrinsic heterogeneity, patient stratification models based on transcriptomic and genomic signatures, with partially overlapping subgroups, have been established. Besides molecular alterations, PDAC tumours show a strong desmoplastic response, resulting in profound metabolic reprogramming involving increased glucose and amino acid consumption, as well as lipid scavenging and biosynthesis. Interestingly, recent works have also revealed the existence of metabolic subtypes with differential prognosis within PDAC, which correlated to defined molecular subclasses in patients: lipogenic subtype correlated with a classical/progenitor signature, while glycolytic tumours associated with the highly aggressive basal/squamous profile. Bioinformatic analyses have demonstrated that the representative genes of each metabolic subtype are up-regulated in PDAC samples and predict patient survival. This suggests a relationship between the genetic signature, metabolic profile, and aggressiveness of the tumour. Considering all this, defining metabolic subtypes represents a clear opportunity for patient stratification considering tumour functional behaviour independently of their mutational background. MDPI 2020-12-21 /pmc/articles/PMC7767410/ /pubmed/33371431 http://dx.doi.org/10.3390/jcm9124128 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Espiau-Romera, Pilar Courtois, Sarah Parejo-Alonso, Beatriz Sancho, Patricia Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title | Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title_full | Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title_fullStr | Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title_full_unstemmed | Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title_short | Molecular and Metabolic Subtypes Correspondence for Pancreatic Ductal Adenocarcinoma Classification |
title_sort | molecular and metabolic subtypes correspondence for pancreatic ductal adenocarcinoma classification |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767410/ https://www.ncbi.nlm.nih.gov/pubmed/33371431 http://dx.doi.org/10.3390/jcm9124128 |
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