Abstract |
Pancreatic neuroendocrine tumors (PanNETs) represent a clinically challenging disease because these tumors vary in clinical presentation, natural history, and prognosis. Novel prognostic biomarkers are needed to improve patient stratification and treatment options. Several putative prognostic and/or predictive biomarkers (eg, alternative lengthening of telomeres, alpha-thalassemia/mental retardation, X-linked (ATRX)/Death Domain Associated Protein (DAXX) loss) have been independently validated. Additionally, recent transcriptomic and epigenetic studies focusing on endocrine differentiation have identified PanNET subtypes that display similarities to either α-cells or β-cells and differ in clinical outcomes. Thus, future prospective studies that incorporate genomic and epigenetic biomarkers are warranted and have translational potential for individualized therapeutic and surveillance strategies.
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Authors | Wenzel M Hackeng, Hussein A Assi, Florine H M Westerbeke, Lodewijk A A Brosens, Christopher M Heaphy |
Journal | Surgical pathology clinics
(Surg Pathol Clin)
Vol. 15
Issue 3
Pg. 541-554
(Sep 2022)
ISSN: 1875-9157 [Electronic] United States |
PMID | 36049835
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2022 Elsevier Inc. All rights reserved. |
Chemical References |
- Adaptor Proteins, Signal Transducing
- Biomarkers
- Co-Repressor Proteins
- Molecular Chaperones
- Nuclear Proteins
- X-linked Nuclear Protein
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Topics |
- Adaptor Proteins, Signal Transducing
(genetics)
- Biomarkers
- Co-Repressor Proteins
(genetics)
- Humans
- In Situ Hybridization, Fluorescence
- Molecular Chaperones
(genetics)
- Neuroendocrine Tumors
(diagnosis, genetics, pathology)
- Nuclear Proteins
(genetics)
- Pancreatic Neoplasms
(diagnosis, genetics, pathology)
- Prognosis
- Prospective Studies
- X-linked Nuclear Protein
(genetics)
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