Evidence map›Paper›PMID 9626060›Full record

ArticleThe American journal of pathology1998

novH: differential expression in developing kidney and Wilm's tumors.

G Chevalier, H Yeger, C Martinerie, M Laurent, J Alami, P N Schofield, B Perbal

Abstract read
In one paragraph

Article in The American journal of pathology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

61 citing papers in PubMed, 144 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. The CCN axis in cancer development and progression.Journal of cell communication and signaling · 2021
    Review
  5. Article
  6. CCN3 (NOV) Drives Degradative Changes in Aging Articular Cartilage.International journal of molecular sciences · 2020
    Article
  7. Dynamic CCN3 expression in the murine CNS does not confer essential roles in myelination or remyelination.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
  9. Review
  10. Acta histochemica et cytochemica · 2017
    Article
  11. Article
  12. Article
  13. The CCN family of proteins: a 25th anniversary picture.Journal of cell communication and signaling · 2016
    Article
  14. Matricellular protein CCN3 mitigates abdominal aortic aneurysm.The Journal of clinical investigation · 2016
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

G ChevalierLaboratoire d'Oncologie Virale et Moléculaire, INSERM U142 Hôpital Saint-Antoine, Paris, France.
H Yeger
C Martinerie
M Laurent
J Alami
P N Schofield
B Perbal
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously established that the expression of the human nov gene (novH) was altered in Wilms' tumors and that levels of novH and WT1 mRNA were inversely correlated in individual Wilms' tumors. Insofar as novH has been shown to be a target for WT1 regulation, novH might play an important role during normal nephrogenesis and in the development of Wilms' tumors. We now show that during normal nephrogenesis novH protein is tightly associated with differentiation of glomerular podocytes. NovH expression is not restricted to renal differentiation but is also detected in endothelium and neural tissue of the kidney. Our results establish that alteration of novH expression in sporadic and heritable Wilms' tumors is associated with dysregulated expression of both novH mRNA and protein. In general, the highest novH expression was noted in the Wilms' tumor, genitourinary anomalies, aniridia, and mental retardation (WAGR)-associated Wilms' tumors. Expression in the Denys-Drash syndrome (DDS)-associated Wilms' tumors fell within the variable spectrum observed in sporadic Wilms' tumor cases. As in developing kidney podocytes, novH protein was also prominent in the abnormal hypoplastic podocytes from DDS cases and in kidney podocytes adjoining Wilms' tumors. In Wilms' tumors exhibiting heterotypic differentiation, novH protein was expressed at high levels in tumor-derived striated muscle and at lower levels in tumor-derived cartilage. These observations taken together indicate that novH may represent both a marker of podocytic differentiation in kidney and a marker of heterotypic mesenchymal differentiation in Wilms' tumors. In addition, absence or very low levels of WT1 are correlated with higher novH expression, and its variable expression in cases with mutant WT1 (sporadic and DDS) suggests that the potential activation and repression transcriptional functions possessed by WT1 are likely dependent on the specific mutation incurred.

Indexed as

Gene Expression RegulationIntercellular Signaling Peptides and ProteinsAnimalsBlotting, WesternCells, CulturedConnective Tissue Growth FactorDogsGlycosylationGrowth SubstancesHumansImmediate-Early ProteinsImmunohistochemistryIn Situ HybridizationKidneyNephroblastoma Overexpressed ProteinRNA, MessengerCCN2 protein, humanCCN3 protein, humanConnective Tissue Growth FactorGrowth SubstancesImmediate-Early ProteinsIntercellular Signaling Peptides and ProteinsNephroblastoma Overexpressed ProteinRNA, Messenger

Identifiers

PMID9626060
PMCPMC1858457
OpenAlexW1907106379

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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.