Evidence map›Paper›PMID 26186938›Full record

ArticleBlood2015

Leukemic marrow infiltration reveals a novel role for Egr3 as a potent inhibitor of normal hematopoietic stem cell proliferation.

Hui Cheng, Sha Hao, Yanfeng Liu, Yakun Pang, Shihui Ma, Fang Dong, Jing Xu, Guoguang Zheng, Shaoguang Li, Weiping Yuan and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 110 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. EGR3 Promotes Glioblastoma Cell Growth with Upregulation of MYC and CDK1.International journal of molecular sciences · 2025
    Article
  5. Article
  6. Article
  7. EGR3 Inhibits Tumor Progression by Inducing Schwann Cell-Like Differentiation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  8. Article
  9. LinCell proliferation · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. DPP4Leukemia · 2021
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Hui ChengState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China; Center for Stem Cell Medicine, Chinese Academy of Medical Sciences, Tianjin, China;
Sha HaoState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Yanfeng LiuState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Yakun PangState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Shihui MaState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Fang DongState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Jing XuState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Guoguang ZhengState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China;
Shaoguang LiDivision of Hematology/Oncology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA; and.
Weiping YuanState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China; Center for Stem Cell Medicine, Chinese Academy of Medical Sciences, Tianjin, China; Department of Stem Cell and Regenerative Medicine, Peking Union Medical College, Tianjin, China.
Tao ChengState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Collaborative Innovation Center for Cancer Medicine, Tianjin, China; Center for Stem Cell Medicine, Chinese Academy of Medical Sciences, Tianjin, China; Department of Stem Cell and Regenerative Medicine, Peking Union Medical College, Tianjin, China.
Institute of Hematology & Blood Diseases Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNPeking Union Medical College Hospital · CNUniversity of Massachusetts Chan Medical School · US

Funding

Zileuton as a chemopreventive agent for chronic myeloid leukemiaR01CA176179 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LI, SHAOGUANG · 2014 to 2018
$1.7M
NCI NIH HHS R01 CA176179
6 · The paper itself

Abstract

Cytopenias resulting from the impaired generation of normal blood cells from hematopoietic precursors are important contributors to morbidity and mortality in patients with leukemia. However, the process by which normal hematopoietic cells are overtaken by emerging leukemia cells and how different subsets of hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) are distinctly influenced during leukemic cell infiltration is poorly understood. To investigate these important questions, we used a robust nonirradiated mouse model of human MLL-AF9 leukemia to examine the suppression of HSCs and HPCs during leukemia cell expansion in vivo. Among all the hematopoietic subsets, long-term repopulating HSCs were the least reduced, whereas megakaryocytic-erythroid progenitors were the most significantly suppressed. Notably, nearly all of the HSCs were forced into a noncycling state in leukemic marrow at late stages, but their reconstitution potential appeared to be intact upon transplantation into nonleukemic hosts. Gene expression profiling and further functional validation revealed that Egr3 was a strong limiting factor for the proliferative potential of HSCs. Therefore, this study provides not only a molecular basis for the more tightened quiescence of HSCs in leukemia, but also a novel approach for defining functional regulators of HSCs in disease.

Indexed as

AnimalsBone MarrowCell ProliferationEarly Growth Response Protein 3Gene Expression ProfilingHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansLeukemia, ExperimentalLeukemic InfiltrationMiceResting Phase, Cell CycleRNA, MessengerRNA, NeoplasmSpleenEarly Growth Response Protein 3Egr3 protein, mouseRNA, MessengerRNA, Neoplasm

Identifiers

PMID26186938
PMCPMC4574014
OpenAlexW2159035471

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.