Evidence map›Paper›PMID 30679322›Full record

ArticleHaematologica2019

ZEB2 and LMO2 drive immature T-cell lymphoblastic leukemia via distinct oncogenic mechanisms.

Steven Goossens, Jueqiong Wang, Cedric S Tremblay, Jelle De Medts, Sara T'Sas, Thao Nguyen, Jesslyn Saw, Katharina Haigh, David J Curtis, Pieter Van Vlierberghe and 3 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.3field-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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Development of anMolecular therapy. Methods & clinical development · 2023
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. LMO2 expression is frequent in T-lymphoblastic leukemia and correlates with survival, regardless of T-cell stage.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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

13 authors at 4 institutions in 3 countries.

Steven GoossensDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium steven.goossens@ugent.be.
Jueqiong WangMammalian Functional Genetics Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Cedric S TremblayStem Cell Research Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Jelle De MedtsDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Sara T'SasDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Thao NguyenMammalian Functional Genetics Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Jesslyn SawStem Cell Research Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Katharina HaighMammalian Functional Genetics Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
David J CurtisStem Cell Research Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Pieter Van VlierbergheDepartment of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Geert BerxDepartment for Biomedical Molecular Biology, VIB-UGent Center for Inflammation Research (IRC), Ghent, Belgium.
Tom TaghonDepartment of Diagnostic Sciences, Ghent University, Ghent, Belgium.
Jody J HaighMammalian Functional Genetics Group, Australian Centre for Blood Diseases, Monash University, Melbourne, VIC, Australia.
Monash University · AUGhent University · BEVIB-UGent Center for Inflammation Research · BEResearch Institute in Oncology and Hematology · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ZEB1 and ZEB2 are structurally related E-box binding homeobox transcription factors that induce epithelial to mesenchymal transitions during development and disease. As such, they regulate cancer cell invasion, dissemination and metastasis of solid tumors. In addition, their expression is associated with the gain of cancer stem cell properties and resistance to therapy. Using conditional loss-of-function mice, we previously demonstrated that

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBiomarkersCell Line, TumorCell Self RenewalCell Transformation, NeoplasticDisease Models, AnimalGene Expression Regulation, LeukemicHematopoiesisHumansImmunohistochemistryInterleukin-7 Receptor alpha SubunitLIM Domain ProteinsMiceNeoplasm GradingNeoplastic Stem CellsAdaptor Proteins, Signal TransducingBiomarkersIL7R protein, humanInterleukin-7 Receptor alpha SubunitLIM Domain ProteinsLMO2 protein, humanProto-Oncogene ProteinsZEB2 protein, humanZinc Finger E-box Binding Homeobox 2

Identifiers

PMID30679322
PMCPMC6669144
OpenAlexW2914988374

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.