Deconstructing pancreatic cancer using next generation-omic technologies: from discovery to knowledge-guided platforms for better patient management
Comprehensive molecular landscaping studies reveal a potentially brighter future for pancreatic ductal adenocarcinoma (PDAC) patients. Blood-borne biomarkers obtained from minimally invasive “liquid biopsies” are now being trialled for early disease detection and to track responses to therapy. Integ...
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| Main Authors: | , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
13 January 2022
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| In: |
Frontiers in cell and developmental biology
Year: 2022, Volume: 9, Pages: 1-15 |
| ISSN: | 2296-634X |
| DOI: | 10.3389/fcell.2021.795735 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3389/fcell.2021.795735 Verlag, lizenzpflichtig, Volltext: https://www.frontiersin.org/articles/10.3389/fcell.2021.795735 |
| Author Notes: | Daniel Schreyer, John P. Neoptolemos, Simon T. Barry and Peter Bailey |
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| 520 | |a Comprehensive molecular landscaping studies reveal a potentially brighter future for pancreatic ductal adenocarcinoma (PDAC) patients. Blood-borne biomarkers obtained from minimally invasive “liquid biopsies” are now being trialled for early disease detection and to track responses to therapy. Integrated genomic and transcriptomic studies using resectable tumour material have defined intrinsic patient subtypes and actionable genomic segments that promise a shift towards genome-guided patient management. Multimodal mapping of PDAC using spatially resolved single cell transcriptomics and imaging techniques has identified new potentially therapeutically actionable cellular targets and is providing new insights into PDAC tumour heterogeneity. Despite these rapid advances, defining biomarkers for patient selection remain limited. This review examines the current PDAC cancer biomarker ecosystem (identified in tumour and blood) and explores how advances in single cell sequencing and spatially resolved imaging modalities are being used to uncover new targets for therapeutic intervention and are transforming our understanding of this difficult to treat disease. | ||
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| 700 | 1 | |a Bailey, Peter |e VerfasserIn |4 aut | |
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