Evidence map›Paper›PMID 14981541›Full record

ArticleOncogene2004

Autocrine stimulation by osteopontin plays a pivotal role in the expression of the mitogenic and invasive phenotype of RET/PTC-transformed thyroid cells.

Maria Domenica Castellone, Angela Celetti, Valentina Guarino, Anna Maria Cirafici, Fulvio Basolo, Riccardo Giannini, Enzo Medico, Mogens Kruhoffer, Torben F Orntoft, Francesco Curcio and 3 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 46 citations in OpenAlex.

  1. Deletion of p18Stem cell research & therapy · 2025
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. 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
  7. Article
  8. Inflammation in thyroid oncogenesis.American journal of cancer research · 2012
    Article
  9. Review
  10. Article
  11. Gene expression profiling of papillary thyroid carcinoma identifies transcripts correlated with BRAF mutational status and lymph node metastasis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
    Article
  12. Article
  13. Article
  14. Induction of a proinflammatory program in normal human thyrocytes by the RET/PTC1 oncogene.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  15. Article
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

13 authors at 5 institutions in 2 countries.

Maria Domenica CastelloneDipartimento di Biologia e Patologia Cellulare e Molecolare, University Federico II c/o Istituto di Endocrinologia ed Oncologia Sperimentale del CNR, Naples, Italy.
Angela Celetti
Valentina Guarino
Anna Maria Cirafici
Fulvio Basolo
Riccardo Giannini
Enzo Medico
Mogens Kruhoffer
Torben F Orntoft
Francesco Curcio
Alfredo Fusco
Rosa Marina Melillo
Massimo Santoro
Institute for Experimental Endocrinology and Oncology · ITAarhus University Hospital · DKUniversity of Pisa · ITUniversity of Turin · ITUniversity of Udine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Papillary thyroid carcinomas are characterized by rearrangements of the RET receptor tyrosine kinase generating RET/PTC oncogenes. Here we show that osteopontin (OPN), a secreted glycoprotein, is a major RET/PTC-induced transcriptional target in PC Cl 3 thyroid follicular cells. OPN upregulation depended on the integrity of the RET/PTC kinase and tyrosines Y1015 and Y1062, two major RET/PTC autophosphorylation sites. RET/PTC also induced a strong overexpression of CD44, a cell surface signalling receptor for OPN. Upregulation of CD44 was dependent on RET/PTC Y1062, as well. Constitutive OPN overexpression or treatment with exogenous recombinant OPN sharply increased proliferation, Matrigel invasion and spreading in collagen gels of RET/PTC-transformed PC Cl 3 cells. These effects were impaired by the treatment of PC Cl 3-RET/PTC cells with OPN- and CD44-locking antibodies. Thus, RET/PTC signalling triggers an autocrine loop involving OPN and CD44 that sustains proliferation and invasion of transfomed PC Cl 3 thyrocytes.

Indexed as

Gene Expression Regulation, NeoplasticCarcinoma, PapillaryCell DivisionCell Line, TumorCell Transformation, NeoplasticCollagenCollagen Type IDNADrug CombinationsHumansHyaluronan ReceptorsLamininNeoplasm InvasivenessOsteopontinPhenotypePhosphorylationCollagenCollagen Type IDNADrug CombinationsHyaluronan ReceptorsLamininmatrigelOsteopontinProteoglycansProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRecombinant ProteinsSialoglycoproteinsSPP1 protein, humanTyrosine

Identifiers

PMID14981541
OpenAlexW2004994163

What OpenQuestion holds

Textmetadata
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.