Evidence map›Paper›PMID 17369819›Full record

ArticleNature cell biology2007

Oestrogen signalling inhibits invasive phenotype by repressing RelB and its target BCL2.

Xiaobo Wang, Karine Belguise, Nathalie Kersual, Kathrin H Kirsch, Nora D Mineva, Florence Galtier, Dany Chalbos, Gail E Sonenshein

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 198 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Role of Fra-2 in cancer.Cell death and differentiation · 2024
    Review
  7. Review
  8. Methylation ofMedComm · 2023
    Article
  9. Article
  10. Review
  11. Phenanthroindolizidine Alkaloids Isolated fromInternational journal of molecular sciences · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Predictors of mammographic microcalcifications.International journal of cancer · 2021
    Article
  17. Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Xiaobo WangDepartment of Biochemistry, Boston University School of Medicine, Boston, MA 02118, USA.
Karine Belguise
Nathalie Kersual
Kathrin H Kirsch
Nora D Mineva
Florence Galtier
Dany Chalbos
Gail E Sonenshein
Boston University · USUniversité de Montpellier · FRInserm · FR

Funding

Signaling Pathways in Stages of TumorigenesisP01ES011624 · NIEHS · TUFTS UNIVERSITY BOSTON · PI SONENSHEIN, GAIL E. · 2001 to 2012
$11.4M
EXPRESSION OF ONCOGENES &IGA GENES IN TRANSFORMED CELLSR01CA036355 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SONENSHEIN, GAIL E · 1985 to 2007
$2.1M
NCI NIH HHS CA36355NCI NIH HHS R01 CA036355NIEHS NIH HHS ES11624NIEHS NIH HHS P01 ES011624
6 · The paper itself

Abstract

Aberrant constitutive expression of c-Rel, p65 and p50 NF-kappaB subunits has been reported in over 90% of breast cancers. Recently, we characterized a de novo RelB NF-kappaB subunit synthesis pathway, induced by the cytomegalovirus (CMV) IE1 protein, in which binding of p50-p65 NF-kappaB and c-Jun-Fra-2 AP-1 complexes to the RELB promoter work in synergy to potently activate transcription. Although RelB complexes were observed in mouse mammary tumours induced by either ectopic c-Rel expression or carcinogen exposure, little is known about RelB in human breast disease. Here, we demonstrate constitutive de novo RelB synthesis is selectively active in invasive oestrogen receptor alpha (ERalpha)-negative breast cancer cells. ERalpha signalling reduced levels of functional NF-kappaB and Fra-2 AP-1 and inhibited de novo RelB synthesis, leading to an inverse correlation between RELB and ERalpha gene expression in human breast cancer tissues and cell lines. Induction of Bcl-2 by RelB promoted the more invasive phenotype of ERalpha-negative cancer cells. Thus, inhibition of de novo RelB synthesis represents a new mechanism whereby ERalpha controls epithelial to mesenchymal transition (EMT).

Indexed as

AnimalsBlotting, NorthernBreast NeoplasmsCell Line, TumorCell MovementCell Transformation, NeoplasticElectrophoretic Mobility Shift AssayEstrogen Receptor alphaEstrogensFemaleFos-Related Antigen-2Gene Expression Regulation, NeoplasticHumansImmunoblottingMiceMicroscopy, FluorescenceEstrogen Receptor alphaEstrogensFos-Related Antigen-2NF-kappa BProto-Oncogene Proteins c-bcl-2Transcription Factor RelB

Identifiers

PMID17369819
PMCPMC2394707
OpenAlexW2112528220

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.