Evidence map›Paper›PMID 31182782›Full record

ArticleLeukemia2019

The neuropeptide receptor calcitonin receptor-like (CALCRL) is a potential therapeutic target in acute myeloid leukemia.

Linus Angenendt, Eike Bormann, Caroline Pabst, Vijay Alla, Dennis Görlich, Leonie Braun, Kim Dohlich, Christian Schwöppe, Stefan K Bohlander, Maria Francisca Arteaga and 24 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Origin and stepwise evolution of vertebrate lungs.Nature ecology & evolution · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Interfering withAnnals of translational medicine · 2022
    Article
  16. Identification of Novel Genes for Cell Fusion during Osteoclast Formation.International journal of molecular sciences · 2022
    Article
  17. Article
  18. Journal of oncology · 2022
    Article
  19. Article
  20. 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

34 authors at 12 institutions in 4 countries.

Linus Angenendt *Department of Medicine A, University Hospital Münster, Münster, Germany. linus.angenendt@ukmuenster.de.ORCID http://orcid.org/0000-0003-2502-9910
Eike Bormann *Institute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
Caroline PabstDepartment of Medicine V, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-9716-5909
Vijay AllaDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Dennis GörlichInstitute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
Leonie BraunDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Kim DohlichDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Christian SchwöppeDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Stefan K BohlanderLeukaemia & Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, University of Auckland, Auckland, New Zealand.ORCID http://orcid.org/0000-0002-2202-9088
Maria Francisca ArteagaDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Klaus WethmarDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Wolfgang HartmannGerhard-Domagk-Institute of Pathology, University Hospital Münster, Münster, Germany.
Adrian AngenendtDepartment of Biophysics, Faculty of Medicine, Centre for Integrative Physiology and Molecular Medicine (CIPMM), Saarland University, Homburg, Germany.
Torsten KesslerDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Rolf M MestersDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Matthias StelljesDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Maja Rothenberg-ThurleyDepartment of Medicine III, University Hospital Grosshadern, LMU Munich, Munich, Germany.
Karsten SpiekermannDepartment of Medicine III, University Hospital Grosshadern, LMU Munich, Munich, Germany.
Josée HébertThe Leucegene Project at Institute for Research in Immunology and Cancer, University of Montreal, Montreal, QC, Canada.
Guy SauvageauThe Leucegene Project at Institute for Research in Immunology and Cancer, University of Montreal, Montreal, QC, Canada.
Peter J M ValkDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Bob LöwenbergDepartment of Hematology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Hubert ServeDepartment of Hematology and Oncology, University Hospital Frankfurt, Frankfurt, Germany.
Carsten Müller-TidowDepartment of Medicine V, University Hospital Heidelberg, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7166-5232
Georg LenzDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Bernhard J WörmannDepartment of Hematology, Oncology and Tumor Immunology, Charité University Medicine, Campus Virchow, Berlin, Germany.
M Christina SauerlandInstitute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
Wolfgang HiddemannDepartment of Medicine III, University Hospital Grosshadern, LMU Munich, Munich, Germany.
Wolfgang E BerdelDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Utz KrugDepartment of Medicine 3, Klinikum Leverkusen, Leverkusen, Germany.
Klaus H MetzelerDepartment of Medicine III, University Hospital Grosshadern, LMU Munich, Munich, Germany.
Jan-Henrik MikeschDepartment of Medicine A, University Hospital Münster, Münster, Germany.
Tobias Herold *Department of Medicine III, University Hospital Grosshadern, LMU Munich, Munich, Germany. tobias.herold@med.uni-muenchen.de.ORCID http://orcid.org/0000-0002-9615-9432
Christoph Schliemann *Department of Medicine A, University Hospital Münster, Münster, Germany. christoph.schliemann@ukmuenster.de.
University Hospital Münster · DELMU Klinikum · DEUniversity of Münster · DEErasmus University Rotterdam · NLHeidelberg University · DEHôpital Maisonneuve-Rosemont · CACharité - Universitätsmedizin Berlin · DEGoethe University Frankfurt · DEHelmholtz Zentrum München · DEKlinikum Leverkusen · DESaarland University · DEUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcitonin receptor-like (CALCRL) is a G-protein-coupled neuropeptide receptor involved in the regulation of blood pressure, angiogenesis, cell proliferation, and apoptosis, and is currently emerging as a novel target for the treatment of migraine. This study characterizes the role of CALCRL in acute myeloid leukemia (AML). We analyzed CALCRL expression in collectively more than 1500 well-characterized AML patients from five international cohorts (AMLCG, HOVON, TCGA, Leucegene, and UKM) and evaluated associations with survival. In the AMLCG analytic cohort, increasing transcript levels of CALCRL were associated with decreasing complete remission rates (71.5%, 53.7%, 49.6% for low, intermediate, high CALCRL expression), 5-year overall (43.1%, 26.2%, 7.1%), and event-free survival (29.9%, 15.8%, 4.7%) (all P < 0.001). CALCRL levels remained associated with all endpoints on multivariable regression analyses. The prognostic impact was confirmed in all validation sets. Genes highly expressed in CALCRL

Indexed as

Biomarkers, TumorAdultAgedAged, 80 and overAnimalsAntineoplastic AgentsBiopsyCalcitonin Receptor-Like ProteinFemaleFollow-Up StudiesGenetic VariationHumansImmunohistochemistryLeukemia, Myeloid, AcuteMaleMiceAntineoplastic AgentsBiomarkers, TumorCalcitonin Receptor-Like ProteinCALCRL protein, human

Identifiers

PMID31182782
OpenAlexW2952863579

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.