Evidence map›Paper›PMID 9176404›Full record

ArticleThe American journal of pathology1997

Phenotypic diversity of neoplastic chondrocytes and extracellular matrix gene expression in cartilaginous neoplasms.

T Aigner, S Dertinger, S I Vornehm, J Dudhia, K von der Mark, T Kirchner

Abstract read
In one paragraph

Article in The American journal of pathology, 1997. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

  1. Review
  2. Review
  3. Selection of Effective Therapies Using Three-DimensionalFrontiers in molecular biosciences · 2020
    Article
  4. Article
  5. Genetic alterations in chondrosarcomas - keys to targeted therapies?Cellular oncology (Dordrecht, Netherlands) · 2014
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. New cell lines with chondrocytic phenotypes from human chondrosarcoma.Virchows Archiv : an international journal of pathology · 2004
    Article
  12. Chondroma of epithelial cell origin.The American journal of pathology · 2003
    Article
  13. Article
  14. 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

6 authors.

T AignerInstitute of Pathology, University of Erlangen-Nürnberg, Germany.
S Dertinger
S I Vornehm
J Dudhia
K von der Mark
T Kirchner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondrocyte differentiation is characterized by distinct cellular phenotypes, which can be identified by specific extracellular matrix gene expression profiles. By applying in situ analysis on the mRNA and protein level in a series of benign and malignant human chondrogenic neoplasms, we were able to identify for the first time different phenotypes of neoplastic chondrocytes in vivo: 1) mature chondrocytes, which synthesized the characteristic cartilaginous extracellular tumor matrix, 2) cells resembling hypertrophic chondrocytes of the fetal growth plate, 3) cells resembling so-called dedifferentiated chondrocytes, and 4) well differentiated chondrocytic cells, which expressed type I collagen, indicating the presence of post-hypertrophic differentiated neoplastic chondrocytes. Chondrocytes exhibiting a range of phenotypes were found to be present in the same neoplasm. The different observed phenotypes, including the dedifferentiated phenotype, were in contrast to the anaplastic cells of high-grade chondrosarcomas. Comparison of expression data with tumor morphology revealed a relationship between the cellular phenotypes, the tumor matrix composition, and the matrix and cell morphology within the neoplasms. The distinctly different phenotypes of neoplastic chondrocytes are the basis of the characteristic high biochemical and morphological heterogeneity of chondroid neoplasms and shed light on their biological and clinical behavior.

Indexed as

Gene Expression Regulation, NeoplasticAggrecansChondromaChondrosarcomaCollagenExtracellular Matrix ProteinsGrowth PlateHumansImmunohistochemistryIn Situ HybridizationLectins, C-TypePhenotypeProteinsProteoglycan Link ProteinProteoglycansRNA, MessengerAggrecansCollagenExtracellular Matrix ProteinsLectins, C-TypeProteinsProteoglycan Link ProteinProteoglycansRNA, MessengerS100 Proteins

Identifiers

PMID9176404
PMCPMC1858327

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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.