Evidence map›Paper›PMID 25907675›Full record

ArticleDiagnostic pathology2015

Cyclin D1 in well differentiated thyroid tumour of uncertain malignant potential.

Monika Lamba Saini, Birgit Weynand, Jacques Rahier, Michel Mourad, Marc Hamoir, Etienne Marbaix

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Monika Lamba SainiAnatomie pathologique, Cliniques universitaires Saint- Luc, Université catholique de Louvain, Avenue Hippocrate, 10/T-1, Brussels, 1200, Belgium. monikalamba@gmail.com.
Birgit WeynandAnatomie pathologique, CHU Dinant-Godinne, Université catholique de Louvain, Avenue Docteur G. Thérasse, 1, Yvoir, 5530, Belgium. birgitweynand@uclouvain.be.
Jacques RahierAnatomie pathologique, Cliniques universitaires Saint- Luc, Université catholique de Louvain, Avenue Hippocrate, 10/T-1, Brussels, 1200, Belgium. jacques.rahier@uclouvain.be.
Michel MouradService de transplantation rénale et chirurgie endocrinologique, Cliniques universitaires Saint-Luc, Université catholique de Louvain, B-1200, Bruxelles, Belgium. michel.mourad@uclouvain.be.
Marc HamoirService d'oto-rhino-laryngologie et chirurgie cervico-faciale, Cliniques universitaires Saint-Luc, Université catholique de Louvain, B-1200, Bruxelles, Belgium. marc.hamoir@uclouvain.be.
Etienne MarbaixAnatomie pathologique, Cliniques universitaires Saint- Luc, Université catholique de Louvain, Avenue Hippocrate, 10/T-1, Brussels, 1200, Belgium. etienne.marbaix@uclouvain.be.
Cliniques Universitaires Saint-Luc · BEUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEncapsulated follicular tumours with equivocal papillary thyroid carcinoma (PTC) type nuclear features continue to remain a challenge despite the recent attempts to classify these borderline lesions. The term 'well differentiated tumour of uncertain malignant potential (WDT-UMP)' was introduced to classify these tumours. The present study aimed to evaluate the role of a cell cycle regulator like cyclin D1 in these tumours along with assessment of other well established PTC markers like galectin-3, HBME-1, CK19.

methodsThirteen cases of metastatic PTC, papillary microcarcinoma and follicular variant of PTC (FVPTC) were identified from a histological review of 510 cases. In addition, 13 cases of a subset of follicular adenomatoid nodules with focal areas showing nuclear features characteristic of PTC, identified as WDT-UMP, were also analyzed. Immunohistochemical analysis of galectin-3, HBME-1, CK19 and the proliferation markers Ki67 and cyclin D1 was performed. Lesions were analyzed for cyclin D1 gene amplification by fluorescent in-situ hybridization.

resultsAll WDT-UMP lesions showed immunolabelling of cyclin D1, Ki67; 11/ 13 cases showed immunolabelling of CK19; 10/13 cases showed immunolabelling of HBME-1 and 4/13 cases showed immunolabelling of galectin-3. Surrounding benign adenomatoid areas showed no to faint focal staining in all thirteen cases of cyclin D1, HBME-1 and galectin-3. A low rate of cyclin D1 gene amplification was identified in a significant proportion of cells in the WDT-UMP lesions as compared to surrounding benign adenomatoid areas.

conclusionsIncreased expression of cyclin D1 and amplification of its gene along with immunolabelling of HBME-1 in WDT-UMP lesions showing cytological features of papillary thyroid carcinoma within follicular adenomatoid nodules suggest that these areas could correspond to a precursor lesion of follicular variant of PTC. Overexpression of cyclin D1, associated with the amplification of the gene suggests that these WDT-UMP lesions are an intermediate between the benign and malignant groups making this group of lesions a reliable precursor of FVPTC. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1851820807142117.

Indexed as

Cell DifferentiationAdenocarcinoma, FollicularAdenomaAdolescentAdultAntigens, NeoplasmBiomarkers, TumorBiopsyBlood ProteinsCarcinomaCarcinoma, PapillaryCyclin D1FemaleGalectin 3GalectinsGene AmplificationAntigens, NeoplasmBiomarkers, TumorBlood ProteinsCCND1 protein, humanCyclin D1Galectin 3GalectinsHBME-1 antigenKeratin-19Ki-67 AntigenLGALS3 protein, human

Identifiers

PMID25907675
PMCPMC4407836
OpenAlexW1969041849

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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.