Evidence map›Paper›PMID 12057919›Full record

ArticleThe American journal of pathology2002

Assessment of RET/PTC oncogene activation and clonality in thyroid nodules with incomplete morphological evidence of papillary carcinoma: a search for the early precursors of papillary cancer.

Alfredo Fusco, Gennaro Chiappetta, Pei Hui, Ginesa Garcia-Rostan, Lauren Golden, Barbara K Kinder, Deborah A Dillon, Ada Giuliano, Anna Maria Cirafici, Massimo Santoro and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 148 citations in OpenAlex.

  1. Review
  2. The promising role and prognostic value of miR-198 in human diseases.American journal of translational research · 2022
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
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  11. Interleukins as markers of inflammation in malignant and benign thyroid disease.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2014
    Article
  12. Interleukin 22 polymorphisms and papillary thyroid cancer.Journal of endocrinological investigation · 2013
    Observational
  13. Article
  14. Article
  15. Article
  16. Inflammation in thyroid oncogenesis.American journal of cancer research · 2012
    Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Alfredo FuscoCentro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Ricerche c/o Dipartimento di Biologia e Patologia Cellulare e Molecolare, Università di Napoli Federico II, Naples, Italy.
Gennaro Chiappetta
Pei Hui
Ginesa Garcia-Rostan
Lauren Golden
Barbara K Kinder
Deborah A Dillon
Ada Giuliano
Anna Maria Cirafici
Massimo Santoro
Juan Rosai
Giovanni Tallini
Yale University · USInstitute for Experimental Endocrinology and Oncology · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITSpanish National Cancer Research Centre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noninvasive thyroid nodules that exhibit borderline morphological signs of papillary cancer are difficult to diagnose and we do not know if they represent papillary carcinoma precursor lesions. Forty-six such nodules were analyzed for RET activation by immunohistochemistry and, in selected cases, by reverse transcriptase-polymerase chain reaction performed on RNA extracted after laser capture microdissection (LCM) of the tumor foci with and without papillary carcinoma features and positive RET immunoreactivity. RET immunoreactivity was identified, at least focally, in 30 of 46 (65.2%) of the nodules where it closely paralleled the morphological changes. Enough RNA was obtained after LCM in seven samples. RET/PTC1 or RET/PTC3 were detected in microscopic foci with papillary carcinoma features in most of the thyroid nodules (five of seven cases). No RET/PTC1 or RET/PTC3 rearrangements were detected in areas of the same tumors that lacked the cytological alterations. Analysis of clonality in the same nodules selected for LCM demonstrated that two were monoclonal and six were polyclonal. We conclude that RET activation closely parallels the morphological changes, that it is restricted to those areas of the tumor with the cytological alterations and that it is detectable in both mono- and polyclonal tumors. Although the finding of microscopic foci indicative of papillary carcinoma in a hyperplastic or adenomatous nodule does not justify the interpretation of the entire lesion as papillary carcinoma, it is possible that such foci may precede the development of invasive papillary cancer.

Indexed as

Drosophila ProteinsTranscription Factors3T3 CellsAnimalsBase SequenceCarcinoma, PapillaryCloning, MolecularGene Expression Regulation, NeoplasticGenetic MarkersHumansMembrane ProteinsMiceMolecular Sequence DataNeoplasm InvasivenessNuclear Receptor CoactivatorsOncogene ProteinsDrosophila ProteinsGenetic MarkersMembrane ProteinsNCOA4 protein, humanNuclear Receptor CoactivatorsOncogene ProteinsOncogene Proteins, FusionPatched-1 ReceptorPatched ReceptorsProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-retPtch1 protein, mouseReceptor Protein-Tyrosine KinasesReceptors, Cell SurfaceRet protein, DrosophilaRet protein, mouseret-PTC fusion oncoproteins, humanTranscription Factors

Identifiers

PMID12057919
PMCPMC1850819
OpenAlexW1596319495

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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.