Evidence map›Paper›PMID 30270123›Full record

ArticleCancer cell2018

HOXA9 Reprograms the Enhancer Landscape to Promote Leukemogenesis.

Yuqing Sun, Bo Zhou, Fengbiao Mao, Jing Xu, Hongzhi Miao, Zhenhua Zou, Le Tran Phuc Khoa, Younghoon Jang, Sheng Cai, Matthew Witkin and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 174 citations in OpenAlex.

  1. Article
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  6. CharacterizingCancers · 2026
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  14. Cancers · 2025
    Review
  15. Article
  16. Review
  17. Molecular principles underlying aggressive cancers.Signal transduction and targeted therapy · 2025
    Review
  18. Getting the right combination to break the epigenetic code.Nature reviews. Clinical oncology · 2025
    Review
  19. Review
  20. Pioneering biomimetic biomaterial for leukemia therapy enhancement: a review.Frontiers in bioengineering and biotechnology · 2025
    Review

36 more citing papers are in PubMed but not listed here.

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

17 authors at 5 institutions in 1 country.

Yuqing SunDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Bo ZhouDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Fengbiao MaoDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Jing XuDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Hongzhi MiaoDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Zhenhua ZouDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Le Tran Phuc KhoaDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Younghoon JangNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Sheng CaiMemorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Matthew WitkinMemorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Richard KocheMemorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Kai GeNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Gregory R DresslerDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Ross L LevineMemorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Scott A ArmstrongDana Farber Cancer Institute, Boston Children's Hospital and Harvard Medical School, Boston, MA 02215, USA.
Yali DouDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA; Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI 48109, USA. Electronic address: yalid@med.umich.edu.
Jay L HessDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA. Electronic address: jayhess@iu.edu.
University of Michigan · USMemorial Sloan Kettering Cancer Center · USNational Institutes of Health · USBoston Children's Hospital · USIndiana University Health · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Regulation of PPARgamma Expression and Adipogenesis by PTIP-Associated FactorsZIADK075003 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GE, KAI · 2009 to 2025
$17.6M
Research Supplement to Promote Diversity in Health Related ResearchR01DK054740 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DRESSLER, GREGORY R · 1999 to 2024
$9.0M
Epigenetic Regulation of Kidney DevelopmentR01DK073722 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DRESSLER, GREGORY R · 2006 to 2020
$4.6M
Function of MLL in transcription regulationR01GM082856 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DOU, YALI · 2009 to 2023
$4.0M
New Therapeutic Targets in AMLR01CA151425 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HESS, JAY L. · 2011 to 2015
$1.7M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA151425NIDDK NIH HHS R01 DK054740NIDDK NIH HHS R01 DK073722NIGMS NIH HHS R01 GM082856
6 · The paper itself

Abstract

Aberrant expression of HOXA9 is a prominent feature of acute leukemia driven by diverse oncogenes. Here we show that HOXA9 overexpression in myeloid and B progenitor cells leads to significant enhancer reorganizations with prominent emergence of leukemia-specific de novo enhancers. Alterations in the enhancer landscape lead to activation of an ectopic embryonic gene program. We show that HOXA9 functions as a pioneer factor at de novo enhancers and recruits CEBPα and the MLL3/MLL4 complex. Genetic deletion of MLL3/MLL4 blocks histone H3K4 methylation at de novo enhancers and inhibits HOXA9/MEIS1-mediated leukemogenesis in vivo. These results suggest that therapeutic targeting of HOXA9-dependent enhancer reorganization can be an effective therapeutic strategy in acute leukemia with HOXA9 overexpression.

Indexed as

AnimalsCell Transformation, NeoplasticEnhancer Elements, GeneticHomeodomain ProteinsHumansLeukemia, Myeloid, AcuteMethylationPromoter Regions, Genetichomeobox protein HOXA9Homeodomain Proteinsacute leukemiade novo enhancerepigeneticshistone methylationHOXA9KMT2MLLpioneer factortranscription factor

Identifiers

PMID30270123
PMCPMC6179449
OpenAlexW2893367264

What OpenQuestion holds

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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.