Evidence map›Paper›PMID 34321607›Full record

ArticleLeukemia2022

The RNA-binding protein IGF2BP3 is critical for MLL-AF4-mediated leukemogenesis.

Tiffany M Tran, Julia Philipp, Jaspal Singh Bassi, Neha Nibber, Jolene M Draper, Tasha L Lin, Jayanth Kumar Palanichamy, Amit Kumar Jaiswal, Oscar Silva, May Paing and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Translational cancer research · 2026
    Article
  12. Article
  13. IGF2BP3 recognizes mThe EMBO journal · 2026
    Article
  14. Article
  15. IGF2BP3 remodels the microRNA targeting landscape in MLL-AF4 leukemia.bioRxiv : the preprint server for biology · 2025
    Article
  16. Review
  17. Article
  18. IGF2BP3 As a Prognostic Biomarker and Regulator of Metastasis in Merkel Cell Carcinoma.JID innovations : skin science from molecules to population health · 2025
    Article
  19. FTO controls CD8Cell death & disease · 2025
    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

14 authors at 3 institutions in 2 countries.

Tiffany M TranDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.ORCID http://orcid.org/0000-0003-2163-3520
Julia PhilippDepartment of Molecular, Cellular and Developmental Biology, UCSC, Santa Cruz, CA, 95064, USA.
Jaspal Singh BassiDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.
Neha NibberDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.
Jolene M DraperDepartment of Molecular, Cellular and Developmental Biology, UCSC, Santa Cruz, CA, 95064, USA.
Tasha L LinDivision of Hematology/Oncology, Department of Medicine, UCLA, Los Angeles, CA, 90095, USA.ORCID http://orcid.org/0000-0003-4281-4152
Jayanth Kumar PalanichamyDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.ORCID http://orcid.org/0000-0002-3903-7252
Amit Kumar JaiswalDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.
Oscar SilvaDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
May PaingDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA.
Jennifer KingDivision of Rheumatology, Department of Medicine, UCLA, Los Angeles, CA, 90095, USA.
Sol KatzmanUCSC Genomics Institute, Santa Cruz, CA, 95064, USA.
Jeremy R SanfordDepartment of Molecular, Cellular and Developmental Biology, UCSC, Santa Cruz, CA, 95064, USA.
Dinesh S RaoDepartment of Pathology & Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, 90095, USA. DRao@mednet.ucla.edu.ORCID http://orcid.org/0000-0002-0794-9337
University of California, Los Angeles · USUniversity of California, Santa Cruz · USStanford University · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 1991 to 2018
$39.9M
TUMOR CELL SURFACES AND CHROMOSOMEST32CA009056 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Gay M Crooks, David A. Nathanson · 1985 to 2026
$10.5M
UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
Protein-RNA interactions in cancerR01CA264986 · NCI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Dinesh S. Rao, Jeremy Robert Sanford · 2021 to 2026
$3.7M
Regulation of mRNA FateR35GM130361 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Jeremy Robert Sanford · 2019 to 2026
$3.1M
Characterizing tumor suppressive functions of microRNAs in B-cell neoplasiaR01CA166450 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RAO, DINESH S · 2013 to 2017
$2.5M
Unraveling the Function of RNA-Binding proteins in B-lympoblastic LeukemiaR21CA197441 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RAO, DINESH S · 2016 to 2017
$368k
NCI NIH HHS P30 CA016042NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA166450NCI NIH HHS R01 CA264986NCI NIH HHS R21 CA197441NCI NIH HHS T32 CA009056NCI NIH HHS T32 CA009120NIAID NIH HHS P30 AI028697NIGMS NIH HHS R35 GM130361
6 · The paper itself

Abstract

Despite recent advances in therapeutic approaches, patients with MLL-rearranged leukemia still have poor outcomes. Here, we find that the RNA-binding protein IGF2BP3, which is overexpressed in MLL-translocated leukemia, strongly amplifies MLL-Af4-mediated leukemogenesis. Deletion of Igf2bp3 significantly increases the survival of mice with MLL-Af4-driven leukemia and greatly attenuates disease, with a minimal impact on baseline hematopoiesis. At the cellular level, MLL-Af4 leukemia-initiating cells require Igf2bp3 for their function in leukemogenesis. At the molecular level, IGF2BP3 regulates a complex posttranscriptional operon governing leukemia cell survival and proliferation. IGF2BP3-targeted mRNA transcripts include important MLL-Af4-induced genes, such as those in the Hoxa locus, and the Ras signaling pathway. Targeting of transcripts by IGF2BP3 regulates both steady-state mRNA levels and, unexpectedly, pre-mRNA splicing. Together, our findings show that IGF2BP3 represents an attractive therapeutic target in this disease, providing important insights into mechanisms of posttranscriptional regulation in leukemia.

Indexed as

Gene Expression Regulation, LeukemicAnimalsApoptosisCarcinogenesisCell ProliferationDNA-Binding ProteinsFemaleHistone-Lysine N-MethyltransferaseLeukemia, ExperimentalMiceMice, Inbred C57BLMice, KnockoutMyeloid-Lymphoid Leukemia ProteinNuclear ProteinsOncogene Proteins, FusionRNA-Binding ProteinsAff1 protein, mouseDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseIgf2bp3 protein, mouseKmt2a protein, mouseMyeloid-Lymphoid Leukemia ProteinNuclear ProteinsOncogene Proteins, FusionRNA-Binding Proteins

Identifiers

PMID34321607
PMCPMC8727287
OpenAlexW3185040741

What OpenQuestion holds

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Registered trials

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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.