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Current status of molecular diagnostic approaches using liquid biopsy
Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Nature Singapore
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423147/ https://www.ncbi.nlm.nih.gov/pubmed/37470859 http://dx.doi.org/10.1007/s00535-023-02024-4 |
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author | Takahashi, Kenji Takeda, Yohei Ono, Yusuke Isomoto, Hajime Mizukami, Yusuke |
author_facet | Takahashi, Kenji Takeda, Yohei Ono, Yusuke Isomoto, Hajime Mizukami, Yusuke |
author_sort | Takahashi, Kenji |
collection | PubMed |
description | Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMN), arise through multiple steps of driver gene alterations in KRAS, TP53, CDKN2A, SMAD4, or GNAS. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity. |
format | Online Article Text |
id | pubmed-10423147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-104231472023-08-14 Current status of molecular diagnostic approaches using liquid biopsy Takahashi, Kenji Takeda, Yohei Ono, Yusuke Isomoto, Hajime Mizukami, Yusuke J Gastroenterol Review Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive and lethal cancers, and developing an efficient and reliable approach for its early-stage diagnosis is urgently needed. Precancerous lesions of PDAC, such as pancreatic intraepithelial neoplasia (PanIN) and intraductal papillary mucinous neoplasms (IPMN), arise through multiple steps of driver gene alterations in KRAS, TP53, CDKN2A, SMAD4, or GNAS. Hallmark mutations play a role in tumor initiation and progression, and their detection in bodily fluids is crucial for diagnosis. Recently, liquid biopsy has gained attention as an approach to complement pathological diagnosis, and in addition to mutation signatures in cell-free DNA, cell-free RNA, and extracellular vesicles have been investigated as potential diagnostic and prognostic markers. Integrating such molecular information to revise the diagnostic criteria for pancreatic cancer can enable a better understanding of the pathogenesis underlying inter-patient heterogeneity, such as sensitivity to chemotherapy and disease outcomes. This review discusses the current diagnostic approaches and clinical applications of genetic analysis in pancreatic cancer and diagnostic attempts by liquid biopsy and molecular analyses using pancreatic juice, duodenal fluid, and blood samples. Emerging knowledge in the rapidly advancing liquid biopsy field is promising for molecular profiling and diagnosing pancreatic diseases with significant diversity. Springer Nature Singapore 2023-07-20 2023 /pmc/articles/PMC10423147/ /pubmed/37470859 http://dx.doi.org/10.1007/s00535-023-02024-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Takahashi, Kenji Takeda, Yohei Ono, Yusuke Isomoto, Hajime Mizukami, Yusuke Current status of molecular diagnostic approaches using liquid biopsy |
title | Current status of molecular diagnostic approaches using liquid biopsy |
title_full | Current status of molecular diagnostic approaches using liquid biopsy |
title_fullStr | Current status of molecular diagnostic approaches using liquid biopsy |
title_full_unstemmed | Current status of molecular diagnostic approaches using liquid biopsy |
title_short | Current status of molecular diagnostic approaches using liquid biopsy |
title_sort | current status of molecular diagnostic approaches using liquid biopsy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10423147/ https://www.ncbi.nlm.nih.gov/pubmed/37470859 http://dx.doi.org/10.1007/s00535-023-02024-4 |
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