Evidence map›Paper›PMID 17110463›Full record

ArticleBlood2007

Expression of a non-DNA-binding isoform of Helios induces T-cell lymphoma in mice.

Zheng Zhang, C Scott Swindle, John T Bates, Rose Ko, Claudiu V Cotta, Christopher A Klug

Abstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Helios-controller of Treg stability and function.Translational cancer research · 2016
    Article
  11. Article
  12. Phenotype and regulation of immunosuppressive Vδ2-expressing γδ T cells.Cellular and molecular life sciences : CMLS · 2014
    Article
  13. Article
  14. Article
  15. Article
  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

6 authors.

Zheng ZhangDepartment of Microbiology, Division of Developmental and Clinical Immunology, University of Alabama at Birmingham, AL, USA.
C Scott Swindle
John T Bates
Rose Ko
Claudiu V Cotta
Christopher A Klug

Funding

IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
Genetic mechanisms regulating B-lymphocyte commitmentR01AI055667 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KLUG, CHRISTOPHER · 2004 to 2008
$1.8M
IKAROS COMPLEX AND LYMPHOID DEVELOPMENTR01DK055650 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KLUG, CHRISTOPHER A · 1999 to 2002
$691k
NIAID NIH HHS R01 AI055667NIAID NIH HHS R01AI055667NIAID NIH HHS T32 AI007051NIAID NIH HHS T32AI07051NIDDK NIH HHS R01DK55650
6 · The paper itself

Abstract

Helios is a zinc-finger protein belonging to the Ikaros family of transcriptional regulators. It is expressed, along with Ikaros, throughout early stages of thymocyte development where it quantitatively associates with Ikaros through C-terminal zinc-finger domains that mediate heterodimerization between Ikaros family members. To understand the role of Helios in T-cell development, we used a retroviral vector to express full-length Helios or a Helios isoform that lacked the N-terminal DNA-binding domain in hematopoietic progenitor cells of reconstituted mice. Constitutive expression of full-length Helios resulted in an inhibition of T-cell development at the double-negative stage within the thymus. Although expression of the DNA-binding mutant of Helios did not contribute to developmental abnormalities at early times after transplantation, 60% of animals that expressed the Helios DNA-binding mutant developed an aggressive and transplantable T-cell lymphoma 4 to 10 months after transplantation. These results demonstrate a vital function for Helios in maintaining normal homeostasis of developing T cells and formally show that non-DNA-binding isoforms of Helios are lymphomagenic if aberrantly expressed within the T-cell lineage.

Indexed as

Gene ExpressionAnimalsCell DifferentiationCell ProliferationCells, CulturedCell Transformation, NeoplasticDNA-Binding ProteinsKiller Cells, NaturalLymphoma, T-CellMiceMice, Inbred C57BLMutationProtein IsoformsThymus GlandTranscription FactorsDNA-Binding ProteinsProtein IsoformsTranscription FactorsZfpn1a2 protein, mouse

Identifiers

PMID17110463
PMCPMC1801072

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.