Evidence map›Paper›PMID 23335373›Full record

ArticleBlood2013

Ikaros inhibits megakaryopoiesis through functional interaction with GATA-1 and NOTCH signaling.

Sébastien Malinge, Clarisse Thiollier, Timothy M Chlon, Louis C Doré, Lauren Diebold, Olivier Bluteau, Vinciane Mabialah, William Vainchenker, Philippe Dessen, Susan Winandy and 2 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Multifaceted roles ofFrontiers in oncology · 2024
    Review
  7. Review
  8. Article
  9. IKAROS in Acute Leukemia: A Positive Influencer or a Mean Hater?International journal of molecular sciences · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. GermlineExpert review of clinical immunology · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Sébastien MalingeDivision of Hematology/Oncology, Northwestern University, Chicago, IL 60611, USA.
Clarisse Thiollier
Timothy M Chlon
Louis C Doré
Lauren Diebold
Olivier Bluteau
Vinciane Mabialah
William Vainchenker
Philippe Dessen
Susan Winandy
Thomas Mercher
John D Crispino
Northwestern University · USWeatherford College · USInserm · FRUniversité Paris Cité · FR

Funding

CORE: ADMINISTRATIVEP50GM081892 · NIGMS · UNIVERSITY OF CHICAGO · PI WHITE, KEVIN P. · 2008 to 2013
$15.9M
Mechanisms of Leukemogenesis in Down SyndromeR01CA101774 · NCI · UNIVERSITY OF CHICAGO · PI CRISPINO, JOHN D · 2003 to 2021
$6.1M
NCI NIH HHS R01 CA101774NIGMS NIH HHS P50 GM081892
6 · The paper itself

Abstract

The transcription factor Ikaros regulates the development of hematopoietic cells. Ikaros-deficient animals fail to develop B cells and display a T-cell malignancy, which is correlated with altered Notch signaling. Recently, loss of Ikaros was associated with progression of myeloproliferative neoplasms to acute myeloid leukemia and increasing evidence shows that Ikaros is also critical for the regulation of myeloid development. Previous studies showed that Ikaros-deficient mice have increased megakaryopoiesis, but the molecular mechanism of this phenomenon remains unknown. Here, we show that Ikaros overexpression decreases NOTCH-induced megakaryocytic specification, and represses expression of several megakaryocytic genes including GATA-1 to block differentiation and terminal maturation. We also demonstrate that Ikaros expression is differentially regulated by GATA-2 and GATA-1 during megakaryocytic differentiation and reveal that the combined loss of Ikzf1 and Gata1 leads to synthetic lethality in vivo associated with prominent defects in erythroid cells and an expansion of megakaryocyte progenitors. Taken together, our observations demonstrate an important functional interplay between Ikaros, GATA factors, and the NOTCH signaling pathway in specification and homeostasis of the megakaryocyte lineage.

Indexed as

AnimalsCell DifferentiationCell ProliferationCells, CulturedDown-RegulationEmbryo, MammalianGATA1 Transcription FactorGene Expression Regulation, DevelopmentalIkaros Transcription FactorMegakaryocytesMiceMice, KnockoutModels, BiologicalProtein BindingReceptors, NotchSignal TransductionGata1 protein, mouseGATA1 Transcription FactorIkaros Transcription FactorReceptors, NotchZfpn1a1 protein, mouse

Identifiers

PMID23335373
PMCPMC3612856
OpenAlexW2052469849

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.