Evidence map›Paper›PMID 25822260›Full record

ArticlePloS one2015

Mitochondrial dynamics protein Drp1 is overexpressed in oncocytic thyroid tumors and regulates cancer cell migration.

André Ferreira-da-Silva, Cristina Valacca, Elisabete Rios, Helena Pópulo, Paula Soares, Manuel Sobrinho-Simões, Luca Scorrano, Valdemar Máximo, Silvia Campello

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
9.9field-weighted citation impact, top 1% of its field
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

116 citing papers in PubMed, 223 citations in OpenAlex.

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  7. Dysregulation of Mitochondrial Function in Cancer Cells.International journal of molecular sciences · 2025
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56 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

André Ferreira-da-SilvaInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Pathology, Medical Faculty of University of Porto, Porto, Portugal.
Cristina ValaccaDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Elisabete RiosInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Pathology, Medical Faculty of University of Porto, Porto, Portugal; Department of Pathology, Hospital S. João, Porto, Portugal.
Helena PópuloInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal.
Paula SoaresInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Pathology, Medical Faculty of University of Porto, Porto, Portugal.
Manuel Sobrinho-SimõesInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Pathology, Medical Faculty of University of Porto, Porto, Portugal; Department of Pathology, Hospital S. João, Porto, Portugal.
Luca ScorranoDepartment of Biology, University of Padua, Padua, Italy; Dulbecco Telethon Institute, Venetian Institute of Molecular Medicine, Padua, Italy; IRCCS Fondazione Santa Lucia, Rome, Italy.
Valdemar MáximoInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal; Department of Pathology, Medical Faculty of University of Porto, Porto, Portugal.
Silvia CampelloDepartment of Biology, University of Rome Tor Vergata, Rome, Italy; IRCCS Fondazione Santa Lucia, Rome, Italy.
Universidade do Porto · PTFondazione Santa Lucia · ITUniversity of Padua · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncocytic cell tumors are characterized by the accumulation of morphologically abnormal mitochondria in their cells, suggesting a role for abnormal mitochondrial biogenesis in oncocytic cell transformation. Little is known about the reason for the dysmorphology of accumulated mitochondria. The proteins regulating the morphology of mitochondria, the "mitochondria-shaping" proteins, can modulate their size and number; however, nothing is known hitherto about a possible involvement of mitochondrial dynamics in oncocytic cell transformation in tumors. Our aim was to assess the status of the mitochondria morphology and its role in oncocytic cell transformation. We therefore evaluated the expression pattern of the main mitochondrial fusion and fission proteins in a series of thyroid cell tumor samples, as well as in thyroid tumor cell lines, with and without oncocytic cell features. The expression of mitochondrial fusion (Opa1, Mfn1 and Mfn2) and fission (Drp1 and Fis1) proteins were evaluated by immunohistochemistry (IHC) in a series of 88 human thyroid tumors. In vitro studies, for comparative purposes and to deepen the study, were performed using TPC1--a papillary thyroid carcinoma derived cell line--and XTC.UC1, an oncocytic follicular thyroid carcinoma-derived cell line. Both IHC and in vitro protein analyses showed an overall increase in the levels of "mitochondrial-shaping" proteins in oncocytic thyroid tumors. Furthermore, overexpression of the pro-fission protein Drp1 was found to be associated with malignant oncocytic thyroid tumors. Interestingly, genetic and pharmacological blockage of Drp1 activity was able to influence thyroid cancer cells' migration/invasion ability, a feature of tumor malignancy. In this study we show that unbalanced mitochondrial dynamics characterize the malignant features of thyroid oncocytic cell tumors, and participate in the acquisition of the migrating phenotype.

Indexed as

Adenoma, OxyphilicCell Line, TumorCell MovementDynaminsGene Expression Regulation, NeoplasticGTP PhosphohydrolasesHumansMembrane ProteinsMicrotubule-Associated ProteinsMitochondriaMitochondrial DynamicsMitochondrial ProteinsThyroid NeoplasmsTissue Array AnalysisDNM1L protein, humanDynaminsFIS1 protein, humanGTP PhosphohydrolasesMembrane ProteinsMicrotubule-Associated ProteinsMitochondrial Proteins

Identifiers

PMID25822260
PMCPMC4379140
OpenAlexW2023234570

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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.