Evidence map›Paper›PMID 31064876›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Heterogeneity in refractory acute myeloid leukemia.

Sachi Horibata, Gege Gui, Justin Lack, Christin B DeStefano, Michael M Gottesman, Christopher S Hourigan

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 65 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Sachi HoribataLaboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; sachi.horibata@nih.gov mgottesman@nih.gov hourigan@nih.gov.
Gege GuiLaboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20814.
Justin LackNIAID Collaborative Bioinformatics Resource, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Christin B DeStefanoLaboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20814.
Michael M GottesmanLaboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; sachi.horibata@nih.gov mgottesman@nih.gov hourigan@nih.gov.ORCID 0000-0001-8908-2097
Christopher S HouriganLaboratory of Myeloid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20814; sachi.horibata@nih.gov mgottesman@nih.gov hourigan@nih.gov.
National Institutes of Health · US

Funding

Detection, prevention and treatment of acute myeloid leukemia (AML) relapse.ZIAHL006163 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HOURIGAN, CHRISTOPHER · 2013 to 2023
$21.0M
Genetic Analysis of the Multidrug Resistance Phenotype in Tumor CellsZIABC005598 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GOTTESMAN, MICHAEL · 2009 to 2025
$11.9M
6 · The paper itself

Abstract

Successful clinical remission to therapy for acute myeloid leukemia (AML) is required for long-term survival to be achieved. Despite trends in improved survival due to better supportive care, up to 40% of patients will have refractory disease, which has a poorly understood biology and carries a dismal prognosis. The development of effective treatment strategies has been hindered by a general lack of knowledge about mechanisms of chemotherapy resistance. Here, through transcriptomic analysis of 154 cases of treatment-naive AML, three chemorefractory patient groups with distinct expression profiles are identified. A classifier, four key refractory gene signatures (RG4), trained based on the expression profile of the highest risk refractory patients, validated in an independent cohort (

Indexed as

Drug Resistance, NeoplasmInduction ChemotherapyAdultAgedAntineoplastic AgentsCohort StudiesFemaleFlavonoidsGene Expression ProfilingGenetic HeterogeneityHumansLeukemia, Myeloid, AcuteMaleMiddle AgedNuclear ProteinsNucleophosminalvocidibAntineoplastic AgentsFlavonoidsNuclear ProteinsNucleophosminPiperidinesacute myeloid leukemiacancer heterogeneitydrug resistance

Identifiers

PMID31064876
PMCPMC6535032
OpenAlexW2944433013

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.