Evidence map›Paper›PMID 12386822›Full record

ArticleOncogene2002

Increased incidence of ERBB2 overexpression and TP53 mutation in inflammatory breast cancer.

Elizabeth Turpin, Ivan Bièche, Philippe Bertheau, Louis-François Plassa, Florence Lerebours, Anne de Roquancourt, Martine Olivi, Marc Espié, Michel Marty, Rosette Lidereau and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Genetic association ofOncoTargets and therapy · 2019
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. How do I treat inflammatory breast cancer?Current treatment options in oncology · 2013
    Article
  14. Estrogen receptor prevents p53-dependent apoptosis in breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  15. Article
  16. Association of inflammatory and noninflammatory breast cancer with socioeconomic characteristics in the Surveillance, Epidemiology, and End Results database, 2000-2007.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012
    Article
  17. TP53 status and response to treatment in breast cancers.Journal of biomedicine & biotechnology · 2011
    Review
  18. Review
  19. Article
  20. 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

12 authors at 5 institutions in 1 country.

Elizabeth TurpinService de Biochimie B and CNRS UPR9051, Hôpital Saint Louis, 1, Avenue Claude Vellefaux, F-75475 Paris Cedex 10, France.
Ivan Bièche
Philippe Bertheau
Louis-François Plassa
Florence Lerebours
Anne de Roquancourt
Martine Olivi
Marc Espié
Michel Marty
Rosette Lidereau
Michel Vidaud
Hughes de Thé
Hôpital Saint-Louis · FRInserm · FRCentre National de la Recherche Scientifique · FRLaboratoire de Biologie Moléculaire et Cellulaire des Eucaryotes · FRHôpital René Huguenin · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory breast cancer (IBC) is one of the most aggressive forms of breast cancer. We studied the biological characteristics of these tumours by comparing the overexpression of oncogenes ERBB2, MYC, CCND1 and RHOC and TP53 gene mutation rates in IBC with those found in locally advanced and not otherwise specified breast cancers. The prevalence of the TP53 mutation was much higher in IBC than in the two other types of cancer (57% vs 30). Unexpectedly, however, in IBC tumours, histological grade was independent of TP53 status. In addition, ERBB2 overexpression was twice as frequent in inflammatory as in non-inflammatory tumours, whereas the frequencies of MYC, CCND1 and RHOC overexpression did not vary significantly among the three types of breast cancer. These findings suggest that IBC tumours constitute a distinct subset with a specific pathogenesis. Given the importance of TP53 and ERBB2 in the response to treatments, our observations have important therapeutic implications for the clinical management of IBC patients.

Indexed as

Genes, erbB-2Genes, p53Breast NeoplasmsHumans

Identifiers

PMID12386822
OpenAlexW2331470002

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.