Evidence map›Paper›PMID 18573879›Full record

ArticleMolecular and cellular biology2008

Selection against PUMA gene expression in Myc-driven B-cell lymphomagenesis.

Sean P Garrison, John R Jeffers, Chunying Yang, Jonas A Nilsson, Mark A Hall, Jerold E Rehg, Wen Yue, Jian Yu, Lin Zhang, Mihaela Onciu and 3 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

88 citing papers in PubMed, 143 citations in OpenAlex.

  1. Activating p53Nature communications · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. BCL-2 protein family: attractive targets for cancer therapy.Apoptosis : an international journal on programmed cell death · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. The Common GermlineCancer research · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Cell Death Pathways in Lymphoid Malignancies.Current oncology reports · 2020
    Review
  19. Review
  20. Review

28 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

13 authors at 4 institutions in 2 countries.

Sean P GarrisonDepartment of Biochemistry, St. Jude Children's Research Hospital, 332 N. Lauderdale, Memphis, TN 38105, USA.
John R Jeffers
Chunying Yang
Jonas A Nilsson
Mark A Hall
Jerold E Rehg
Wen Yue
Jian Yu
Lin Zhang
Mihaela Onciu
Jeffery T Sample
John L Cleveland
Gerard P Zambetti
Scripps Research Institute · USSt. Jude Children's Research Hospital · USUniversity of Pittsburgh · USUmeå University · SE

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
PAX3/FKHR IN ALVEOLAR RHABDOMYOSARCOMAP01CA071907 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DOWNING, JAMES R · 1996 to 2005
$10.8M
The Bcl-2/Bcl-X Pathway in Myc-Induced LymphomagenesisR01CA076379 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CLEVELAND, JOHN L. · 1998 to 2012
$3.5M
PUMA-mediated apoptosis in human cancer cellsR01CA106348 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZHANG, LIN · 2004 to 2014
$2.6M
MUTANT P53 GAIN OF FUNCTION IN TURMORIGENISISR01CA063230 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ZAMBETTI, GERARD PAUL · 1995 to 2007
$2.3M
Role of Epstein-Barr Virus in Burkitt LymphomaR01CA073544 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SAMPLE, JEFFERY T · 1996 to 2007
$1.6M
NCI NIH HHS CA63230NCI NIH HHS CA71907NCI NIH HHS CA73544NCI NIH HHS CA76379NCI NIH HHS P01 CA071907NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA063230NCI NIH HHS R01 CA073544NCI NIH HHS R01 CA076379NCI NIH HHS R01 CA106348
6 · The paper itself

Abstract

The p53 tumor suppressor pathway limits oncogenesis by inducing cell cycle arrest or apoptosis. A key p53 target gene is PUMA, which encodes a BH3-only proapoptotic protein. Here we demonstrate that Puma deletion in the Emu-Myc mouse model of Burkitt lymphoma accelerates lymphomagenesis and that approximately 75% of Emu-Myc lymphomas naturally select against Puma protein expression. Furthermore, approximately 40% of primary human Burkitt lymphomas fail to express detectable levels of PUMA and in some tumors this is associated with DNA methylation. Burkitt lymphoma cell lines phenocopy the primary tumors with respect to DNA methylation and diminished PUMA expression, which can be reactivated following inhibition of DNA methyltransferases. These findings establish that PUMA is silenced in human malignancies, and they suggest PUMA as a target for the development of novel chemotherapeutics.

Indexed as

AnimalsApoptosisApoptosis Regulatory ProteinsAzacitidineBase SequenceB-LymphocytesBurkitt LymphomaCell Line, TumorEpigenesis, GeneticGene Expression ProfilingGene Expression Regulation, NeoplasticHistonesHumansMethylationMiceMice, Inbred C57BLApoptosis Regulatory ProteinsAzacitidineBBC3 protein, humanHistonesProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycPUMA protein, mouseTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID18573879
PMCPMC2519737
OpenAlexW1981178222

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.