Evidence map›Paper›PMID 29773641›Full record

ArticleThe Journal of experimental medicine2018

IL1RAP potentiates multiple oncogenic signaling pathways in AML.

Kelly Mitchell, Laura Barreyro, Tihomira I Todorova, Samuel J Taylor, Iléana Antony-Debré, Swathi-Rao Narayanagari, Luis A Carvajal, Joana Leite, Zubair Piperdi, Gopichand Pendurti and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
6.2field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 95 citations in OpenAlex.

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  15. Smoking-Associated Carcinogen-Induced Inflammation Promotes Lung Carcinogenesis via IRAK4 Activation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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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

15 authors at 1 institution in 1 country.

Kelly MitchellDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-1124-7864
Laura BarreyroDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-9515-5579
Tihomira I TodorovaDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Samuel J TaylorDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Iléana Antony-DebréDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Swathi-Rao NarayanagariDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0003-3372-1501
Luis A CarvajalDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Joana LeiteDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Zubair PiperdiDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.
Gopichand PendurtiDepartment of Medicine (Oncology), Division of Hemato-Oncology, Albert Einstein College of Medicine-Montefiore Medical Center, Bronx, NY.
Ioannis MantzarisDepartment of Medicine (Oncology), Division of Hemato-Oncology, Albert Einstein College of Medicine-Montefiore Medical Center, Bronx, NY.
Elisabeth PaiettaDepartment of Medicine (Oncology), Division of Hemato-Oncology, Albert Einstein College of Medicine-Montefiore Medical Center, Bronx, NY.
Amit VermaDepartment of Medicine (Oncology), Division of Hemato-Oncology, Albert Einstein College of Medicine-Montefiore Medical Center, Bronx, NY.
Kira GritsmanDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-1367-1167
Ulrich SteidlDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY ulrich.steidl@einstein.yu.edu.ORCID 0000-0002-9458-1795
Albert Einstein College of Medicine · US

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
ECOG-ACRIN Biospecimen Bank to Support NCTNU24CA196172 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI STANLEY R. HAMILTON, Scott D Jewell · 2015 to 2026
$41.1M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
ECOG-ACRIN INTEGRATED LEUKEMIA TRANSLATIONAL RESEARCH CENTERU10CA180827 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI LEVINE, ROSS L, MELNICK, ARI M. · 2014 to 2018
$3.0M
Mechanisms of Formation and Progression of Preleukemic Stem CellsR01CA217092 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STEIDL, ULRICH · 2017 to 2021
$2.0M
PI3K Isoform Dependence in Adult Hematopoiesis and Myeloid LeukemiaR01CA196973 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GRITSMAN, KIRA · 2016 to 2020
$2.0M
Role of a Novel Homeobox Transcription Factor (HLX) in Acute Myeloid LeukemiaR01CA166429 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STEIDL, ULRICH · 2013 to 2017
$1.9M
NCI NIH HHS R01 CA166429NCI NIH HHS R01 CA196973NCI NIH HHS R01 CA217092NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180827NCI NIH HHS U24 CA196172NIGMS NIH HHS T32 GM007491
6 · The paper itself

Abstract

The surface molecule interleukin-1 receptor accessory protein (IL1RAP) is consistently overexpressed across multiple genetic subtypes of acute myeloid leukemia (AML) and other myeloid malignancies, including at the stem cell level, and is emerging as a novel therapeutic target. However, the cell-intrinsic functions of IL1RAP in AML cells are largely unknown. Here, we show that targeting of IL1RAP via RNA interference, genetic deletion, or antibodies inhibits AML pathogenesis in vitro and in vivo, without perturbing healthy hematopoietic function or viability. Furthermore, we found that the role of IL1RAP is not restricted to the IL-1 receptor pathway, but that IL1RAP physically interacts with and mediates signaling and pro-proliferative effects through FLT3 and c-KIT, two receptor tyrosine kinases with known key roles in AML pathogenesis. Our study provides a new mechanistic basis for the efficacy of IL1RAP targeting in AML and reveals a novel role for this protein in the pathogenesis of the disease.

Indexed as

Signal TransductionAdultAgedAnimalsAntibodiesApoptosisCarcinogenesisCell DifferentiationCell Line, TumorCell ProliferationDown-RegulationFemaleGene DeletionHematopoiesisHumansInterleukin-1 Receptor Accessory ProteinAntibodiesflt3 ligand proteinInterleukin-1 Receptor Accessory ProteinMembrane ProteinsProto-Oncogene Proteins c-kitStem Cell Factor

Identifiers

PMID29773641
PMCPMC5987926
OpenAlexW2803596986

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.