Evidence map›Paper›PMID 30019447›Full record

ReviewEuropean journal of clinical investigation2018

The underestimated role of basophils in Ph

Peter Valent, Hans-Peter Horny, Michel Arock

Open access · hybridAbstract readReview
In one paragraph

Review in European journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
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  5. Article
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  7. Genetic Variants Leading to Urticaria and Angioedema and Associated Biomarkers.The journal of allergy and clinical immunology. In practice · 2023
    Article
  8. Article
  9. Article
  10. Review
  11. Review
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  15. Review
  16. Article
  17. Review
  18. Histamine receptors and cancer pharmacology: an update.British journal of pharmacology · 2020
    Review
  19. The underestimated role of basophils in PhEuropean journal of clinical investigation · 2018
    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

3 authors at 3 institutions in 3 countries.

Peter ValentDivision of Hematology & Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-0456-5095
Hans-Peter HornyInstitute of Pathology, Ludwig Maximilian University, Munich, Germany.
Michel ArockLBPA CNRS UMR8113, Ecole Normale Supérieure de Paris Saclay, Cachan, France.
École Normale Supérieure Paris-Saclay · FRLudwig Boltzmann Institute for Cardiovascular Research · ATLudwig-Maximilians-Universität München · DE

Funding

Austrian National Science Fund F4701-B20Austrian National Science Fund F4704-B20
6 · The paper itself

Abstract

Chronic myeloid leukaemia (CML) is a hematopoietic neoplasm defined by the chromosome translocation t(9;22) and the related oncogene, BCR-ABL1. In most patients, leukaemic cells can be kept under control using BCR-ABL1-targeting drugs. However, many patients relapse which remains a clinical challenge. In particular, patients with advanced (accelerated or blast phase) CML have a poor prognosis. So far, little is known about molecular and cellular interactions and features that contribute to disease progression and drug resistance in CML. One key prognostic factor at diagnosis is marked basophilia. However, although basophils are well-known multifunctional effector cells, their impact in CML remains uncertain. In this article, we discuss the potential role of basophils as active contributors to disease evolution and progression in CML. In particular, basophils serve as a unique source of inflammatory, angiogenic and fibrogenic molecules, such as vascular endothelial growth factor or hepatocyte growth factor. In addition, basophils provide vasoactive substances, like histamine as well as the cytokine-degrading enzyme dipeptidyl-peptidase IV which may promote stem cell mobilization and the extramedullary spread of stem and progenitor cells. Finally, basophils may produce autocrine growth factors for myeloid cells. Understanding the role of basophils in CML evolution and progression may support the development of more effective treatment concepts.

Indexed as

Antigens, NeoplasmBasophilsBiomarkers, TumorDisease ProgressionForecastingHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveNeoplastic Stem CellsTumor MicroenvironmentAntigens, NeoplasmBiomarkers, Tumorbasophiliabasophil leukaemiachronic myeloid leukaemiaprognosticationtryptase

Identifiers

PMID30019447
PMCPMC6175372
OpenAlexW2884698969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.