Evidence map›Paper›PMID 29983867›Full record

ArticleOncotarget2018

MicroRNA analysis of gastroenteropancreatic neuroendocrine tumors and metastases.

Nadine Zimmermann, Juliana Knief, Tim Kacprowski, Pamela Lazar-Karsten, Tobias Keck, Franck Billmann, Sebastian Schmid, Kim Luley, Hendrik Lehnert, Georg Brabant and 1 more

Abstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. The Role of miRNA in the Pathophysiology of Neuroendocrine Tumors.International journal of molecular sciences · 2021
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  19. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Nadine ZimmermannDepartment of Pathology, Section of Hematopathology and Endocrine Pathology, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Juliana KniefDepartment of Pathology, Section of Hematopathology and Endocrine Pathology, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Tim KacprowskiDepartment of Functional Genomics, Interfaculty Institute of Genetics and Functional Genomics, University Medicine Greifswald, Greifswald 17475, Germany.
Pamela Lazar-KarstenDepartment of Pathology, Section of Hematopathology and Endocrine Pathology, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Tobias KeckDepartment of Surgery, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Franck BillmannDepartment of Surgery, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Sebastian SchmidDepartment of Internal Medicine 1, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Kim LuleyDepartment of Internal Medicine 1, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Hendrik LehnertDepartment of Internal Medicine 1, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Georg BrabantDepartment of Internal Medicine 1, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.
Christoph ThornsDepartment of Pathology, Section of Hematopathology and Endocrine Pathology, University Hospital of Schleswig-Holstein, Lübeck 23538, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The incidence of neuroendocrine neoplasias (NEN) continues to increase. Since the primary tumor cannot be diagnosed in some cases of metastatic disease, new biomarkers are clearly needed to find the most probable site of origin. Tissue samples from 79 patients were analyzed and microRNA profiles were generated from a total of 76 primary tumors, 31 lymph node and 14 solid organ metastases. NEN metastases were associated with elevated levels of miR-30a-5p, miR-210, miR-339-3p, miR-345 and miR-660. Three microRNAs showed a strong correlation between proliferation index and metastatic disease in general (miR-150, miR-21 and miR-660). Further, each anatomic location (primary or metastatic) had one or more site-specific microRNAs more highly expressed in these tissues. Comparison between primary tumors and metastases revealed an overlap only in pancreatic (miR-127) and ileal tumors (let-7g, miR-200a and miR-331). This thorough analysis of gastroenteropancreatic neuroendocrine tumors demonstrates site-specific microRNA profiles, correlation with proliferation indices as well as corresponding nodal and distant metastases. Using microRNA profiling might improve NEN diagnostics by linking metastases to a most probable site of origin.

Indexed as

gastroenteropancreatic tumorsmetastatic diseasemicroRNAneuroendocrine neoplasias

Identifiers

PMID29983867
PMCPMC6033345

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.