Small intestinal neuroendocrine tumors lack early genomic drivers, acquire DNA repair defects and harbor hallmarks of low REST expression

The tumorigenesis of small intestinal neuroendocrine tumors (siNETs) is not understood and comprehensive genomic and transcriptomic data sets are limited. Therefore, we performed whole genome and transcriptome analysis of 39 well differentiated siNET samples. Our genomic data revealed a lack of recurrent driver mutations and demonstrated that multifocal siNETs from individual patients can arise genetically independently. We detected germline mutations in Fanconi anemia DNA repair pathway (FANC) genes, involved in homologous recombination (HR) DNA repair, in 9% of patients and found mutational signatures of defective HR DNA repair in late-stage tumor evolution. Furthermore, transcriptomic analysis revealed low expression of the transcriptional repressor REST. Summarizing, we identify a novel common transcriptomic signature of siNETs and demonstrate that genomic alterations alone do not explain initial tumor formation, while impaired DNA repair likely contributes to tumor evolution and represents a potential pharmaceutical target in a subset of patients.

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Publication Details

Journal
Scientific Reports
Published
2025-05-23
DOI
https://doi.org/10.1038/s41598-025-01912-4
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
Field-Weighted Citation Impact
0.00

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article

Small intestinal neuroendocrine tumors lack early genomic drivers, acquire DNA repair defects and harbor hallmarks of low REST expression

I Eichhorn, Bertram Wiedenmann, Shashwat Sahay, Olivia Debnath et al.
Scientific Reports
Neuroendocrine Tumor Research Advances
article

Small intestinal neuroendocrine tumors lack early genomic drivers, acquire DNA repair defects and harbor hallmarks of low REST expression

I Eichhorn, Bertram Wiedenmann, Shashwat Sahay, Olivia Debnath, Roland Eils, Naveed Ishaque, Tomasz Żemojtel, Annika Lehmann, Felix Bolduan, Ute Ungethuem, Catarina Alisa Kunze, Yvonne Giesecke, David Horst, Niklas Müller‐Bötticher, Michael Sigal, Alexandra Wetzel, Christoph Roderburg, Marten Jaeger, Frank Tacke
article en

Abstract

The tumorigenesis of small intestinal neuroendocrine tumors (siNETs) is not understood and comprehensive genomic and transcriptomic data sets are limited. Therefore, we performed whole genome and transcriptome analysis of 39 well differentiated siNET samples. Our genomic data revealed a lack of recurrent driver mutations and demonstrated that multifocal siNETs from individual patients can arise genetically independently. We detected germline mutations in Fanconi anemia DNA repair pathway (FANC) genes, involved in homologous recombination (HR) DNA repair, in 9% of patients and found mutational signatures of defective HR DNA repair in late-stage tumor evolution. Furthermore, transcriptomic analysis revealed low expression of the transcriptional repressor REST. Summarizing, we identify a novel common transcriptomic signature of siNETs and demonstrate that genomic alterations alone do not explain initial tumor formation, while impaired DNA repair likely contributes to tumor evolution and represents a potential pharmaceutical target in a subset of patients.

Scientific ReportsVol. 15(1)
Humboldt-Universität zu Berlin (DE), Düsseldorf University Hospital (DE), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), Deutsches Konsortium für Translationale Krebsforschung (DE), Heinrich Heine University Düsseldorf (DE), Freie Universität Berlin (DE), Charité - Universitätsmedizin Berlin (DE)
Charité – Universitätsmedizin Berlin
Good health and well-being
Openalex Percentile: Top 83%
Neuroendocrine Tumor Research Advances
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