Analysis of miR-29 Serum Levels in Patients with Neuroendocrine Tumors-Results from an Exploratory Study.

biomarker miR-29 neuroendocrine carcinoma neuroendocrine tumor survival

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
06 Sep 2020
Historique:
received: 25 07 2020
revised: 30 08 2020
accepted: 03 09 2020
entrez: 9 9 2020
pubmed: 10 9 2020
medline: 10 9 2020
Statut: epublish

Résumé

Due to its involvement in tumor biology as well as tumor-associated stroma cell responses, recent data suggested a potential role of miR-29 as a biomarker for different malignancies. However, its role in neuroendocrine tumors (NETs) is only poorly understood. We measured circulating levels of miR-29b in 45 patients with NET and compared them to 19 healthy controls. Results were correlated with clinical records. In our cohort of NET patients treated between 2010 and 2019 at our department, miR-29b serum levels were significantly downregulated when compared to healthy control samples. Further, a significant correlation between chromogranin A (CgA) and relative miR-29b levels was noted. However, serum levels of miR-29b were independent of tumor-related factors such as proliferation activity according to Ki-67 index, tumor grading, the TMN stage of malignant tumors, somatostatin receptor expression or clinical features such as functional or non-functional disease and presence of tumor relapse. Finally, in contrast to previous results from other malignancies, miR-29b serum levels were not a significant predictor of overall survival in NET patients. Our data suggest a role for miR-29b serum levels as a previously unrecognized biomarker for diagnosis of NET. However, miR-29 does not allow for predicting tumor stage or patients' outcome.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Due to its involvement in tumor biology as well as tumor-associated stroma cell responses, recent data suggested a potential role of miR-29 as a biomarker for different malignancies. However, its role in neuroendocrine tumors (NETs) is only poorly understood.
METHODS METHODS
We measured circulating levels of miR-29b in 45 patients with NET and compared them to 19 healthy controls. Results were correlated with clinical records.
RESULTS RESULTS
In our cohort of NET patients treated between 2010 and 2019 at our department, miR-29b serum levels were significantly downregulated when compared to healthy control samples. Further, a significant correlation between chromogranin A (CgA) and relative miR-29b levels was noted. However, serum levels of miR-29b were independent of tumor-related factors such as proliferation activity according to Ki-67 index, tumor grading, the TMN stage of malignant tumors, somatostatin receptor expression or clinical features such as functional or non-functional disease and presence of tumor relapse. Finally, in contrast to previous results from other malignancies, miR-29b serum levels were not a significant predictor of overall survival in NET patients.
CONCLUSION CONCLUSIONS
Our data suggest a role for miR-29b serum levels as a previously unrecognized biomarker for diagnosis of NET. However, miR-29 does not allow for predicting tumor stage or patients' outcome.

Identifiants

pubmed: 32899973
pii: jcm9092881
doi: 10.3390/jcm9092881
pmc: PMC7565987
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : German Research Foundation
ID : DFG RO 4317/4-1
Organisme : German Center for Cardiovascular Diseases
ID : DZHK, B18-005Ext

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Auteurs

Burcin Özdirik (B)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Anna K Stueven (AK)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Raphael Mohr (R)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Lukas Geisler (L)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Alexander Wree (A)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Jana Knorr (J)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Münevver Demir (M)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Mihael Vucur (M)

Department of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074 Aachen, Germany.

Sven H Loosen (SH)

Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital, Düsseldorf, Moorenstraße 5, 40225 Düsseldorf, Germany.

Fabian Benz (F)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Markus Reiss (M)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Bertram Wiedenmann (B)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Frank Tacke (F)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Henning Jann (H)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Teresa Hellberg (T)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Christoph Roderburg (C)

Department of Hepatology & Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

Classifications MeSH