Evidence map›Paper›PMID 10602468›Full record

ReviewOncogene1999

Aberrant rel/nfkb genes and activity in human cancer.

B Rayet, C Gélinas

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 437 papers.

0numbers the graph read from it
0cells of the map it votes in
437citing papers in PubMed
18.5field-weighted citation impact, top 1% 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

437 citing papers in PubMed, 1,102 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Sea conch (Food science & nutrition · 2024
    Article
  7. Article
  8. Article
  9. Chronic Treatment withInternational journal of molecular sciences · 2024
    Article
  10. Article
  11. Review
  12. Neuroprotective effects of a novel peptide fromFood science & nutrition · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. NF-kB's contribution to B cell fate decisions.Frontiers in immunology · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Review

377 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

2 authors at 2 institutions in 1 country.

B RayetAdvanced Biotechnology and Medicine, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey, NJ 08854-5638, USA.
C Gélinas
Gorgias Press (United States) · USRutgers, The State University of New Jersey · US

Funding

TRANS-ACTING FUNCTION OF THE V- AND C-REL ONCOPROTEINSR01CA054999 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GELINAS, CELINE · 1996 to 2005
$1.6M
TRANS-ACTING FUNCTION OF THE V- AND C-REL ONCOPROTEINSR29CA054999 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GELINAS, CELINE · 1991 to 1995
–
NCI NIH HHS CA54999
6 · The paper itself

Abstract

Rel/NF-kappaB transcription factors are key regulators of immune, inflammatory and acute phase responses and are also implicated in the control of cell proliferation and apoptosis. Remarkable progress has been made in understanding the signal transduction pathways that lead to the activation of Rel/NF-kappaB factors and the consequent induction of gene expression. Evidence linking deregulated Rel/NF-kappaB activity to oncogenesis in mammalian systems has emerged in recent years, consistent with the acute oncogenicity of the viral oncoprotein v-Rel in animal models. Chromosomal amplification, overexpression and rearrangement of genes coding for Rel/NF-kappaB factors have been noted in many human hematopoietic and solid tumors. Persistent nuclear NF-kappaB activity was also described in several human cancer cell types, as a result of constitutive activation of upstream signaling kinases or mutations inactivating inhibitory IkappaB subunits. Studies point to a correlation between the activation of cellular gene expression by Rel/NF-kappaB factors and their participation in the malignant process. Experiments implicating NF-kappaB in the control of the apoptotic response also support a role in oncogenesis and in the resistance of tumor cells to chemotherapy. This review focuses on the status of the rel, nfkb and ikb genes and their activity in human tumors and their association with the onset or progression of malignancies.

Indexed as

B-Cell Lymphoma 3 ProteinCell DivisionCell SurvivalGene AmplificationGene RearrangementHumansNeoplasmsNF-kappa BProto-Oncogene ProteinsProto-Oncogene Proteins c-relTranscription Factor RelATranscription Factor RelBTranscription FactorsB-Cell Lymphoma 3 ProteinBCL3 protein, humanNF-kappa BProto-Oncogene ProteinsProto-Oncogene Proteins c-relRELB protein, humanTranscription Factor RelATranscription Factor RelBTranscription Factors

Identifiers

PMID10602468
OpenAlexW2027260180

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.