Evidence map›Paper›PMID 28301608›Full record

ArticlePloS one2017

Loss of c-KIT expression in thyroid cancer cells.

Sara Franceschi, Francesca Lessi, Federica Panebianco, Elena Tantillo, Marco La Ferla, Michele Menicagli, Paolo Aretini, Alessandro Apollo, Antonio Giuseppe Naccarato, Ivo Marchetti and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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  13. Identification ofG3 (Bethesda, Md.) · 2020
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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 at 4 institutions in 2 countries.

Sara FranceschiFPS-Pisa Science Foundation, Pisa, Italy.ORCID http://orcid.org/0000-0002-4246-4407
Francesca LessiFPS-Pisa Science Foundation, Pisa, Italy.
Federica PanebiancoDepartment of Translational Research and New Technologies in Medicine and Surgery, University Hospital of Pisa, Pisa, Italy.
Elena TantilloFPS-Pisa Science Foundation, Pisa, Italy.
Marco La FerlaFPS-Pisa Science Foundation, Pisa, Italy.
Michele MenicagliFPS-Pisa Science Foundation, Pisa, Italy.
Paolo AretiniFPS-Pisa Science Foundation, Pisa, Italy.
Alessandro ApolloDepartment of Translational Research and New Technologies in Medicine and Surgery, University Hospital of Pisa, Pisa, Italy.
Antonio Giuseppe NaccaratoDepartment of Translational Research and New Technologies in Medicine and Surgery, University Hospital of Pisa, Pisa, Italy.
Ivo MarchettiDepartment of Translational Research and New Technologies in Medicine and Surgery, University Hospital of Pisa, Pisa, Italy.
Chiara Maria MazzantiFPS-Pisa Science Foundation, Pisa, Italy.
Fondazione Pisa · ITAzienda Ospedaliera Universitaria Pisana · ITTumour Institute of Tuscany · ITUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Papillary thyroid carcinoma is the most frequent histologic type of thyroid tumor. Few studies investigated the role of c-KIT expression in thyroid tumors, suggesting a role for this receptor and its ligand in differentiation and growth control of thyroid epithelium and a receptor loss following malignant transformation. We investigated and correlated c-KIT expression levels and two known markers of thyrocytes differentiation, PAX8 and TTF-1, in malignant and benign cytological thyroid samples. Moreover, we performed functional studies on human papillary thyroid carcinoma cell line to associated c-KIT expression to thyrocytes differentiation and tumor proliferation. c-KIT and PAX8 expression resulted higher in benign samples compared to the malignant ones, and the expression levels of these two genes were significantly correlated to each other. We also observed that c-KIT overexpression led to an increase of PAX8 expression level together with a decrease of proliferation. Furthermore, c-KIT overexpressing cells showed a regression of typical morphological features of malignancy. Taken together these results suggest that c-KIT could be involved in the differentiation of thyroid cells and in tumor progression.

Indexed as

CarcinomaCarcinoma, PapillaryCell DifferentiationCell Line, TumorCell ProliferationHumansNuclear ProteinsPAX8 Transcription FactorProto-Oncogene Proteins c-kitThyroid Cancer, PapillaryThyroid NeoplasmsThyroid Nuclear Factor 1Transcription FactorsNKX2-1 protein, humanNuclear ProteinsPAX8 protein, humanPAX8 Transcription FactorProto-Oncogene Proteins c-kitThyroid Nuclear Factor 1Transcription Factors

Identifiers

PMID28301608
PMCPMC5354407
OpenAlexW2595033379

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.