Evidence map›Paper›PMID 41104964›Full record

ReviewEuropean thyroid journal2025

DICER1 and DGCR8 in thyroid tumorigenesis: miRNA biogenesis and histopathologic diversity.

Lia Rodrigues, Rui Sousa Martins, Valdemar Máximo, Paula Soares, Joao Vinagre, Vania Nosé, Sule Canberk

Abstract readReview
In one paragraph

Review in European thyroid journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Lia RodriguesInstitute for Research and Innovation in Health of the University of Porto (I3S), Porto, Portugal.
Rui Sousa MartinsInstitute for Research and Innovation in Health of the University of Porto (I3S), Porto, Portugal.
Valdemar MáximoInstitute for Research and Innovation in Health of the University of Porto (I3S), Porto, Portugal.
Paula SoaresInstitute for Research and Innovation in Health of the University of Porto (I3S), Porto, Portugal.ORCID https://orcid.org/0000-0001-9607-6998
Joao VinagreInstitute for Research and Innovation in Health of the University of Porto (I3S), Porto, Portugal.
Vania NoséDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Sule CanberkRISE-Health, Department of Pathology, Faculty of Medicine of the University of Porto (FMUP), Porto, Portugal.ORCID https://orcid.org/0000-0002-3736-1323

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This review examines the emerging roles of DICER1 and DGCR8, key components of the miRNA biogenesis pathway, in thyroid pathogenesis, with a particular focus on their association with oncocytic morphology. Recent findings have expanded our understanding of DICER1 syndrome and DGCR8-related thyroid disorders, revealing a broader spectrum of thyroid lesions associated with mutations in these genes than previously recognised. We analyse the current literature on DICER1 and DGCR8 mutations in thyroid pathology, synthesising data from both basic science and pathological studies. The review explores recent findings on oncocytic features in some DICER1-mutated thyroid lesions, acknowledging that this association remains under investigation. The manuscript details the molecular mechanisms underlying DICER1 and DGCR8 mutations, including their impact on miRNA processing and subsequent effects on gene expression and cellular function. We discuss the diverse range of thyroid lesions associated with these mutations, from benign follicular nodular disease to aggressive carcinomas. The clinical implications of these findings are significant, as recognising DICER1 and DGCR8-related thyroid lesions can lead to improved patient management, including genetic counselling and surveillance for other associated malignancies. We propose an algorithm for identifying DICER1-related thyroid lesions, with a focus on oncocytic tumours, to aid clinicians and pathologists in recognising these entities. This emerging field promises to refine the diagnosis, management, and treatment of thyroid disorders associated with miRNA biogenesis pathway alterations, potentially leading to novel diagnostic and therapeutic approaches.

Indexed as

DEAD-box RNA HelicasesMicroRNAsRibonuclease IIIRNA-Binding ProteinsThyroid NeoplasmsCarcinogenesisHumansMutationDEAD-box RNA HelicasesDGCR8 protein, humanDICER1 protein, humanMicroRNAsRibonuclease IIIRNA-Binding ProteinsDGCR8DICER1miRNA biogenesisoncocytic neoplasmsthyroid

Identifiers

PMID41104964
PMCPMC12595409

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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.