Evidence map›Paper›PMID 21785465›Full record

ArticleOncogene2012

Hipk2 cooperates with p53 to suppress γ-ray radiation-induced mouse thymic lymphoma.

J-H Mao, D Wu, I-J Kim, H C Kang, G Wei, J Climent, A Kumar, F G Pelorosso, R DelRosario, E J Huang and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. HIPK2 phosphorylates HDAC3 for NF-κB acetylation to ameliorate colitis-associated colorectal carcinoma and sepsis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. The nutrient sensor OGT regulates Hipk stability and tumorigenic-like activities inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Role of HIPK2 in kidney fibrosis.Kidney international supplements · 2014
    Review
  17. Article
  18. Identification of Hipk2 as an essential regulator of white fat development.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Review
  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

11 authors at 3 institutions in 2 countries.

J-H MaoLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
D Wu
I-J Kim
H C Kang
G Wei
J Climent
A Kumar
F G Pelorosso
R DelRosario
E J Huang
A Balmain
UCSF Helen Diller Family Comprehensive Cancer Center · USSan Francisco VA Medical Center · USLawrence Berkeley National Laboratory · US

Funding

Identification of epithelial tumor susceptiility genesU01CA084244 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BALMAIN, ALLAN · 1999 to 2013
$13.3M
The Role of Fbxw7 in genetic instability and cancerR01CA116481 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MAO, JIAN-HUA · 2008 to 2012
$1.7M
NCI NIH HHS R01 CA116481NCI NIH HHS U01 CA084244NCI NIH HHS U01 CA84244
6 · The paper itself

Abstract

A genome-wide screen for genetic alterations in radiation-induced thymic lymphomas generated from p53+/- and p53-/- mice showed frequent loss of heterozygosity (LOH) on chromosome 6. Fine mapping of these LOH regions revealed three non-overlapping regions, one of which was refined to a 0.2 Mb interval that contained only the gene encoding homeobox-interacting protein kinase 2 (Hipk2). More than 30% of radiation-induced tumors from both p53+/- and p53-/- mice showed heterozygous loss of one Hipk2 allele. Mice carrying a single inactive allele of Hipk2 in the germline were susceptible to induction of tumors by γ-radiation, but most tumors retained and expressed the wild-type allele, suggesting that Hipk2 is a haploinsufficient tumor suppressor gene for mouse lymphoma development. Heterozygous loss of both Hipk2 and p53 confers strong sensitization to radiation-induced lymphoma. We conclude that Hipk2 is a haploinsufficient lymphoma suppressor gene.

Indexed as

AnimalsCarrier ProteinsCell Transformation, NeoplasticChromosomes, MammalianGamma RaysGene Expression Regulation, NeoplasticLoss of HeterozygosityLymphomaMiceMice, Inbred C57BLMice, KnockoutNeoplasms, Radiation-InducedProtein BindingProtein Serine-Threonine KinasesThymus NeoplasmsTumor Suppressor Protein p53Carrier ProteinsHipk2 protein, mouseProtein Serine-Threonine KinasesTumor Suppressor Protein p53

Identifiers

PMID21785465
PMCPMC3307058
OpenAlexW1972130528

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.