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New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer

With recent advances in molecular pathology and the development of new chemotherapy regimens, the knowledge of the molecular alterations of pancreatic ductal adenocarcinoma (PDAC) is becoming appealing for stratifying patients for prognosis and response to a defined treatment. Archival formalin-fixe...

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Autores principales: Archibugi, Livia, Testoni, Sabrina Gloria Giulia, Redegalli, Miriam, Petrone, Maria Chiara, Reni, Michele, Falconi, Massimo, Doglioni, Claudio, Capurso, Gabriele, Arcidiacono, Paolo Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883177/
https://www.ncbi.nlm.nih.gov/pubmed/31798775
http://dx.doi.org/10.4251/wjgo.v11.i11.933
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author Archibugi, Livia
Testoni, Sabrina Gloria Giulia
Redegalli, Miriam
Petrone, Maria Chiara
Reni, Michele
Falconi, Massimo
Doglioni, Claudio
Capurso, Gabriele
Arcidiacono, Paolo Giorgio
author_facet Archibugi, Livia
Testoni, Sabrina Gloria Giulia
Redegalli, Miriam
Petrone, Maria Chiara
Reni, Michele
Falconi, Massimo
Doglioni, Claudio
Capurso, Gabriele
Arcidiacono, Paolo Giorgio
author_sort Archibugi, Livia
collection PubMed
description With recent advances in molecular pathology and the development of new chemotherapy regimens, the knowledge of the molecular alterations of pancreatic ductal adenocarcinoma (PDAC) is becoming appealing for stratifying patients for prognosis and response to a defined treatment. Archival formalin-fixed, paraffin-embedded samples are a useful source of genomic deoxyribonucleic acid; nevertheless, most studies employed formalin-fixed, paraffin-embedded samples deriving from surgical specimens, which are therefore representative of <20% of PDAC patients. Indeed, the development of a reliable methodology for endoscopic ultrasound-guided tissue acquisition, stabilization, and analysis is crucial for the development of molecular markers for clinical use in order to achieve “personalized medicine”. With the development of new needles, this technique is able to retrieve a high quantity and quality of PDAC tissue that can be used not only for diagnosis but also for mutational and transcriptome evaluations and for the development of primary cell or tissue cultures. In the present editorial, we discuss the current knowledge regarding the use of endoscopic ultrasound as a tool to obtain samples for molecular analyses, its possible pitfalls, and its use for the development of disease models such as xenografts or organoids.
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spelling pubmed-68831772019-12-03 New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer Archibugi, Livia Testoni, Sabrina Gloria Giulia Redegalli, Miriam Petrone, Maria Chiara Reni, Michele Falconi, Massimo Doglioni, Claudio Capurso, Gabriele Arcidiacono, Paolo Giorgio World J Gastrointest Oncol Editorial With recent advances in molecular pathology and the development of new chemotherapy regimens, the knowledge of the molecular alterations of pancreatic ductal adenocarcinoma (PDAC) is becoming appealing for stratifying patients for prognosis and response to a defined treatment. Archival formalin-fixed, paraffin-embedded samples are a useful source of genomic deoxyribonucleic acid; nevertheless, most studies employed formalin-fixed, paraffin-embedded samples deriving from surgical specimens, which are therefore representative of <20% of PDAC patients. Indeed, the development of a reliable methodology for endoscopic ultrasound-guided tissue acquisition, stabilization, and analysis is crucial for the development of molecular markers for clinical use in order to achieve “personalized medicine”. With the development of new needles, this technique is able to retrieve a high quantity and quality of PDAC tissue that can be used not only for diagnosis but also for mutational and transcriptome evaluations and for the development of primary cell or tissue cultures. In the present editorial, we discuss the current knowledge regarding the use of endoscopic ultrasound as a tool to obtain samples for molecular analyses, its possible pitfalls, and its use for the development of disease models such as xenografts or organoids. Baishideng Publishing Group Inc 2019-11-15 2019-11-15 /pmc/articles/PMC6883177/ /pubmed/31798775 http://dx.doi.org/10.4251/wjgo.v11.i11.933 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Editorial
Archibugi, Livia
Testoni, Sabrina Gloria Giulia
Redegalli, Miriam
Petrone, Maria Chiara
Reni, Michele
Falconi, Massimo
Doglioni, Claudio
Capurso, Gabriele
Arcidiacono, Paolo Giorgio
New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title_full New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title_fullStr New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title_full_unstemmed New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title_short New era for pancreatic endoscopic ultrasound: From imaging to molecular pathology of pancreatic cancer
title_sort new era for pancreatic endoscopic ultrasound: from imaging to molecular pathology of pancreatic cancer
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883177/
https://www.ncbi.nlm.nih.gov/pubmed/31798775
http://dx.doi.org/10.4251/wjgo.v11.i11.933
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