Evidence map›Paper›PMID 24509510›Full record

ArticleNature immunology2014

Loss of Ikaros DNA-binding function confers integrin-dependent survival on pre-B cells and progression to acute lymphoblastic leukemia.

Ila Joshi, Toshimi Yoshida, Nilamani Jena, Xiaoqing Qi, Jiangwen Zhang, Richard A Van Etten, Katia Georgopoulos

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
20.2field-weighted citation impact, top 1% 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

105 citing papers in PubMed, 162 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. IKAROS Family Transcription Factors in Lymphocyte Differentiation and Function.Advances in experimental medicine and biology · 2024
    Review
  15. Multifaceted roles ofFrontiers in oncology · 2024
    Review
  16. Biomedicines · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Review

45 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

7 authors at 4 institutions in 2 countries.

Ila JoshiCutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, USA.
Toshimi YoshidaCutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, USA.
Nilamani JenaMolecular Oncology Research Institute, Tufts Medical Center, Boston, Massachusetts, USA.
Xiaoqing QiCutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, USA.
Jiangwen ZhangSchool of Biological Sciences, The University of Hong Kong, Hong Kong.
Richard A Van Etten1] Molecular Oncology Research Institute, Tufts Medical Center, Boston, Massachusetts, USA. [2] Present address: Chao Family Comprehensive Cancer Center and Division of Hematology/Oncology, University of California, Irvine, Irvine, California, USA.
Katia GeorgopoulosCutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts, USA.
Massachusetts General Hospital · USHarvard University · USMolecular Oncology (United States) · USUniversity of Hong Kong · HK

Funding

STUDIES OF BCR/ABL LEUKEMOGENESIS IN MICER01CA090576 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAN ETTEN, RICHARD A. · 2001 to 2021
$5.9M
Ikaros and Mi-2 beta interactions in early lymphoid developmentR01AI042254 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 1998 to 2013
$5.3M
Role of IKAROS in the Biology and Therapy of High-Risk Precursor B-Cell LeukemiaR01CA190964 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GEORGOPOULOS, KATIA, VAN ETTEN, RICHARD A. · 2015 to 2019
$2.7M
Ikaros regulation: study on hemo-lymphopoiesisR01CA162092 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GEORGOPOULOS, KATIA · 2011 to 2015
$1.8M
NCI NIH HHS 5R01CA162092-20NCI NIH HHS CA090576NCI NIH HHS R01 CA090576NCI NIH HHS R01 CA162092NCI NIH HHS R01 CA190964NIAID NIH HHS 5R01AI 42254-14NIAID NIH HHS R01 AI042254
6 · The paper itself

Abstract

Deletion of the DNA-binding domain of the transcription factor Ikaros generates dominant-negative isoforms that interfere with its activity and correlate with poor prognosis in human precursor B cell acute lymphoblastic leukemia (B-ALL). Here we found that conditional inactivation of the Ikaros DNA-binding domain in early pre-B cells arrested their differentiation at a stage at which integrin-dependent adhesion to niches augmented signaling via mitogen-activated protein kinases, proliferation and self-renewal and attenuated signaling via the pre-B cell signaling complex (pre-BCR) and the differentiation of pre-B cells. Transplantation of polyclonal Ikaros-mutant pre-B cells resulted in long-latency oligoclonal pre-B-ALL, which demonstrates that loss of Ikaros contributes to multistep B cell leukemogenesis. Our results explain how normal pre-B cells transit from a highly proliferative and stroma-dependent phase to a stroma-independent phase during which differentiation is enabled, and suggest potential therapeutic strategies for Ikaros-mutant B-ALL.

Indexed as

Cell ProliferationAdoptive TransferAnimalsApoptosisCell DifferentiationCell SeparationCell SurvivalDisease ProgressionDNA-Binding ProteinsFlow CytometryFluorescent Antibody TechniqueIkaros Transcription FactorImmunoblottingMiceMice, TransgenicPrecursor Cell Lymphoblastic Leukemia-LymphomaDNA-Binding ProteinsIkaros Transcription FactorZfpn1a1 protein, mouse

Identifiers

PMID24509510
PMCPMC4494688
OpenAlexW2035749206

What OpenQuestion holds

Textmetadata
LicenceTDM
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.