Evidence map›Paper›PMID 26904942›Full record

ArticleCell reports2016

Ezh2 Controls an Early Hematopoietic Program and Growth and Survival Signaling in Early T Cell Precursor Acute Lymphoblastic Leukemia.

Etienne Danis, Taylor Yamauchi, Kristen Echanique, Xi Zhang, Jessica N Haladyna, Simone S Riedel, Nan Zhu, Huafeng Xie, Stuart H Orkin, Scott A Armstrong and 2 more

Abstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Trial
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  10. Cancer discovery · 2020
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  19. Article
  20. Emerging epigenetic-modulating therapies in lymphoma.Nature reviews. Clinical oncology · 2019
    Review
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.

Etienne DanisDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Taylor YamauchiDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Kristen EchaniqueDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Xi ZhangDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Jessica N HaladynaDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Simone S RiedelDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA.
Nan ZhuStem Cell Biology and Hematopoiesis Program, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, WI 53226, USA.
Huafeng XieDana Farber Cancer Institute and Boston Children's Hospital, Harvard Medical School and HHMI, Boston, MA 02115, USA.
Stuart H OrkinDana Farber Cancer Institute and Boston Children's Hospital, Harvard Medical School and HHMI, Boston, MA 02115, USA.
Scott A ArmstrongCancer Biology and Genetics Program, Departments of Medicine and Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Kathrin M BerntDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA; Center for Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, CO 80045, USA. Electronic address: kathrin.bernt@ucdenver.edu.
Tobias NeffDepartment of Pediatrics, Section of Pediatric Hematology/Oncology/Bone Marrow Transplantation, University of Colorado Denver, Aurora, CO 80045, USA; Center for Cancer and Blood Disorders, Children's Hospital Colorado, Aurora, CO 80045, USA. Electronic address: tobias.neff@ucdenver.edu.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Ezh2 in MLL-AF9 mediated acute myeloid leukemiaK08CA154777 · NCI · UNIVERSITY OF COLORADO DENVER · PI NEFF, TOBIAS · 2011 to 2015
$730k
H3K79 Methylation in Hematopoietic Stem Cell Development and MLL-Rearranged LeukK08HL102264 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BERNT, KATHRIN M · 2010 to 2014
$660k
Howard Hughes Medical InstituteNCI NIH HHS K08 CA154777NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA046934NCI NIH HHS P30CA046934NHLBI NIH HHS K08 HL102264NHLBI NIH HHS K08HL102264
6 · The paper itself

Abstract

Early T cell precursor acute lymphoblastic leukemia (ETP-ALL) is an aggressive subtype of ALL distinguished by stem-cell-associated and myeloid transcriptional programs. Inactivating alterations of Polycomb repressive complex 2 components are frequent in human ETP-ALL, but their functional role is largely undefined. We have studied the involvement of Ezh2 in a murine model of NRASQ61K-driven leukemia that recapitulates phenotypic and transcriptional features of ETP-ALL. Homozygous inactivation of Ezh2 cooperated with oncogenic NRASQ61K to accelerate leukemia onset. Inactivation of Ezh2 accentuated expression of genes highly expressed in human ETP-ALL and in normal murine early thymic progenitors. Moreover, we found that Ezh2 contributes to the silencing of stem-cell- and early-progenitor-cell-associated genes. Loss of Ezh2 also resulted in increased activation of STAT3 by tyrosine 705 phosphorylation. Our data mechanistically link Ezh2 inactivation to stem-cell-associated transcriptional programs and increased growth/survival signaling, features that convey an adverse prognosis in patients.

Indexed as

Gene Expression Regulation, LeukemicGenes, rasAnimalsDisease Models, AnimalEnhancer of Zeste Homolog 2 ProteinHistonesHumansInterleukin-6Janus Kinase 1MiceMice, TransgenicPhosphorylationPolycomb Repressive Complex 2Precursor Cells, T-LymphoidPrecursor T-Cell Lymphoblastic Leukemia-LymphomaReceptors, Interleukin-6Eed protein, mouseEnhancer of Zeste Homolog 2 ProteinEzh2 protein, mouseHistonesInterleukin-6interleukin-6, mouseJak1 protein, mouseJanus Kinase 1Polycomb Repressive Complex 2Receptors, Interleukin-6Stat3 protein, mouseSTAT3 Transcription FactorSuz12 protein, mouse

Identifiers

PMID26904942
PMCPMC4790111

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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.