Evidence map›Paper›PMID 28710059›Full record

ArticleBlood2017

A FOXO1-induced oncogenic network defines the AML1-ETO preleukemic program.

Shan Lin, Anetta Ptasinska, Xiaoting Chen, Mahesh Shrestha, Salam A Assi, Paulynn S Chin, Maria R Imperato, B J Aronow, Jingsong Zhang, Matthew T Weirauch and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.7field-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

26 citing papers in PubMed, 38 citations in OpenAlex.

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  7. RUNX1T1 function in cell fate.Stem cell research & therapy · 2022
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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

12 authors at 4 institutions in 2 countries.

Shan LinDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Anetta PtasinskaInstitute of Cancer and Genomic Sciences, College of Medicine and Dentistry, University of Birmingham, Birmingham, United Kingdom.
Xiaoting ChenCenter for Autoimmune Genomics and Etiology and.
Mahesh ShresthaDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Salam A AssiInstitute of Cancer and Genomic Sciences, College of Medicine and Dentistry, University of Birmingham, Birmingham, United Kingdom.
Paulynn S ChinInstitute of Cancer and Genomic Sciences, College of Medicine and Dentistry, University of Birmingham, Birmingham, United Kingdom.
Maria R ImperatoInstitute of Cancer and Genomic Sciences, College of Medicine and Dentistry, University of Birmingham, Birmingham, United Kingdom.
B J AronowDivision of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; and.
Jingsong ZhangDepartment of Pharmacology and Physiology, St. Louis University School of Medicine, St. Louis, MO.
Matthew T WeirauchCenter for Autoimmune Genomics and Etiology and.
Constanze BoniferInstitute of Cancer and Genomic Sciences, College of Medicine and Dentistry, University of Birmingham, Birmingham, United Kingdom.
James C MulloyDivision of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
University of Birmingham · GBCincinnati Children's Hospital Medical Center · USAutoimmune Technologies (United States) · USSaint Louis University · US

Funding

REPRODUCTIVE AND DEVELOPMENTAL TOXICOLOGY RESEARCHP30ES006096 · NIEHS · UNIVERSITY OF CINCINNATI · PI PINNEY, SUSAN MENGEL · 1992 to 2022
$35.4M
VITAMIN K DEFICIENCY IN CHOLESTATIC LIVER DISEASEM01RR008084 · NCRR · CINCINNATI CHILDRENS HOSP MED CTR · PI STRAUSS, ARNOLD W · 1994 to 2009
$20.6M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
Cincinnati Center for Excellence in Molecular HematologyP30DK090971 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI ZHENG, YI · 2010 to 2015
$4.0M
Medical Research Council MR/M009157/1NCRR NIH HHS M01 RR008084NCRR NIH HHS UL1 RR026314NIDDK NIH HHS P30 DK090971NIEHS NIH HHS P30 ES006096
6 · The paper itself

Abstract

Understanding and blocking the self-renewal pathway of preleukemia stem cells could prevent acute myeloid leukemia (AML) relapse. In this study, we show that increased FOXO1 represents a critical mechanism driving aberrant self-renewal in preleukemic cells expressing the t(8;21)-associated oncogene AML1-ETO (AE). Although generally considered as a tumor suppressor, FOXO1 is consistently upregulated in t(8;21) AML. Expression of FOXO1 in human CD34

Indexed as

Gene Regulatory NetworksAnimalsAntigens, CD34Cell Line, TumorCell ProliferationCore Binding Factor Alpha 2 SubunitForkhead Box Protein O1Gene Expression ProfilingGene Expression Regulation, LeukemicGenome, HumanHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMice, SCIDOncogene Proteins, FusionPrecancerous ConditionsAML1-ETO fusion protein, humanAntigens, CD34Core Binding Factor Alpha 2 SubunitForkhead Box Protein O1Oncogene Proteins, FusionRUNX1 Translocation Partner 1 Protein

Identifiers

PMID28710059
PMCPMC5606002
OpenAlexW2734955076

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.