Evidence map›Paper›PMID 15356338›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Marek's disease is a natural model for lymphomas overexpressing Hodgkin's disease antigen (CD30).

S C Burgess, J R Young, B J G Baaten, L Hunt, L N J Ross, M S Parcells, P M Kumar, C A Tregaskes, L F Lee, T F Davison

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

49 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. A Review on the Marek's Disease Outbreak and Its Virulence-RelatedAnimals : an open access journal from MDPI · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Progress on chicken T cell immunity to viruses.Cellular and molecular life sciences : CMLS · 2019
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  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

10 authors at 2 institutions in 1 country.

S C BurgessDepartment of Basic Science, College of Veterinary Medicine, Mississippi State University, P.O. Box 1600, Mississippi State, MS 39762-6100, USA. burgess@cvm.msstate.edu
J R Young
B J G Baaten
L Hunt
L N J Ross
M S Parcells
P M Kumar
C A Tregaskes
L F Lee
T F Davison
Mississippi State University · USUniversity of Delaware · US

Funding

THE EFFECT OF DIELDRIN TREATMENT ON THE EXPRESSION OF SEVERAL GENES OF INTERESTP20RR017661 · NCRR · MISSISSIPPI STATE UNIVERSITY · PI CHAMBERS, JANICE ELAINE · 2002 to 2006
$8.7M
NCRR NIH HHS P20 RR 017661NCRR NIH HHS P20 RR017661
6 · The paper itself

Abstract

Animal models are essential for elucidating the molecular mechanisms of carcinogenesis. Hodgkin's and many diverse non-Hodgkin's lymphomas overexpress the Hodgkin's disease antigen CD30 (CD30(hi)), a tumor necrosis factor receptor II family member. Here we show that chicken Marek's disease (MD) lymphoma cells are also CD30(hi) and are a unique natural model for CD30(hi) lymphoma. Chicken CD30 resembles an ancestral form, and we identify a previously undescribed potential cytoplasmic signaling domain conserved in chicken, human, and mouse CD30. Our phylogeneic analysis defines a relationship between the structures of human and mouse CD30 and confirms that mouse CD30 represents the ancestral mammalian gene structure. CD30 expression by MD virus (MDV)-transformed lymphocytes correlates with expression of the MDV Meq putative oncogene (a c-Jun homologue) in vivo. The chicken CD30 promoter has 15 predicted high-stringency Meq-binding transcription factor recognition motifs, and Meq enhances transcription from the CD30 promoter in vitro. Plasma proteomics identified a soluble form of CD30. CD30 overexpression is evolutionarily conserved and defines one class of neoplastic transformation events, regardless of etiology. We propose that CD30 is a component of a critical intracellular signaling pathway perturbed in neoplastic transformation. Specific anti-CD30 Igs occurred after infection of genetically MD-resistant chickens with oncogenic MDV, suggesting immunity to CD30 could play a role in MD lymphoma regression.

Indexed as

Amino Acid SequenceAnimalsAntigens, CDCell Transformation, NeoplasticChickensConserved SequenceDisease Models, AnimalGene Expression Regulation, NeoplasticHodgkin DiseaseHumansKi-1 AntigenLymphocyte ActivationMardivirusMarek DiseaseMiceMolecular Sequence DataAntigens, CDKi-1 Antigen

Identifiers

PMID15356338
PMCPMC518847
OpenAlexW2112463928

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.