Evidence map›Paper›PMID 29880605›Full record

ArticleHaematologica2018

Pharmacological inhibition of dihydroorotate dehydrogenase induces apoptosis and differentiation in acute myeloid leukemia cells.

Dang Wu, Wanyan Wang, Wuyan Chen, Fulin Lian, Li Lang, Ying Huang, Yechun Xu, Naixia Zhang, Yinbin Chen, Mingyao Liu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.6field-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

44 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 3 countries.

Dang WuShanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, China.
Wanyan WangShanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, China.
Wuyan ChenCAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), China.
Fulin LianCAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), China.
Li LangShanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, China.
Ying HuangGuangdong Institute for Drug Control, Guangzhou, China.
Yechun XuCAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), China.
Naixia ZhangCAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CAS), China.
Yinbin ChenShanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, China.
Mingyao LiuShanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, China.
Ruth NussinovCancer and Inflammation Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, National Cancer Institute at Frederick, MD, USA.
Feixiong ChengCenter for Complex Networks Research and Department of Physics, Northeastern University, Boston, MA, USA huangjin@ecust.edu.cn wqlu@bio.ecnu.edu.cn chengf@ccf.org.
Weiqiang LuShanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, China huangjin@ecust.edu.cn wqlu@bio.ecnu.edu.cn chengf@ccf.org.
Jin HuangShanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, China huangjin@ecust.edu.cn wqlu@bio.ecnu.edu.cn chengf@ccf.org.
East China University of Science and Technology · CNEast China Normal University · CNShanghai Institute of Materia Medica · CNChinese Academy of Sciences · CNCleveland Clinic Lerner College of Medicine · USGuangdong Institute for Drug Control · CNNational Cancer Institute · US

Funding

Protein Structure, Stability, and Amyloid FormationZIABC010440 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2009 to 2025
$11.8M
Method Development: Efficient Computer Vision Based AlgorithmsZIABC010442 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NUSSINOV, RUTH · 2009 to 2025
$2.4M
An individualized network medicine infrastructure for precision cardio-oncologyK99HL138272 · NHLBI · NORTHEASTERN UNIVERSITY · PI CHENG, FEIXIONG · 2017 to 2017
$86k
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENHLBI NIH HHS K99 HL138272
6 · The paper itself

Abstract

Acute myeloid leukemia is a disorder characterized by abnormal differentiation of myeloid cells and a clonal proliferation derived from primitive hematopoietic stem cells. Interventions that overcome myeloid differentiation have been shown to be a promising therapeutic strategy for acute myeloid leukemia. In this study, we demonstrate that CRISPR/Cas9-mediated knockout of dihydroorotate dehydrogenase leads to apoptosis and normal differentiation of acute myeloid leukemia cells, indicating that dihydroorotate dehydrogenase is a potential differentiation regulator and a therapeutic target in acute myeloid leukemia. By screening a library of natural products, we identified a novel dihydroorotate dehydrogenase inhibitor, isobavachalcone, derived from the traditional Chinese medicine

Indexed as

AnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorCell DifferentiationCell Line, TumorCell ProliferationChalconesDihydroorotate DehydrogenaseDisease Models, AnimalDrug SynergismEnzyme ActivationEnzyme InhibitorsGene ExpressionGene Knockdown TechniquesHumansAntineoplastic AgentsBiomarkers, TumorChalconesDihydroorotate DehydrogenaseEnzyme InhibitorsisobavachalconeOxidoreductases Acting on CH-CH Group Donors

Identifiers

PMID29880605
PMCPMC6119157
OpenAlexW2806824289

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.