Evidence map›Paper›PMID 36269299›Full record

ArticleThe Journal of experimental medicine2023

Primary tumor-derived systemic nANGPTL4 inhibits metastasis.

Corinne Hübers, Ashik Ahmed Abdul Pari, Denise Grieshober, Martin Petkov, Alexander Schmidt, Tatjana Messmer, Christian Moritz Heyer, Sebastian Schölch, Stephanie S Kapel, Nicolas Gengenbacher and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
4.8field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  10. Research (Washington, D.C.) · 2024
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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

23 authors at 7 institutions in 4 countries.

Corinne Hübers *European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-8095-866X
Ashik Ahmed Abdul Pari *European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0003-2878-9210
Denise Grieshober *European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-4746-9805
Martin PetkovEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-0325-7982
Alexander SchmidtDepartment of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-3149-2381
Tatjana MessmerDivision of Vascular Oncology and Metastasis, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.ORCID 0000-0003-2466-6192
Christian Moritz HeyerFaculty of Biosciences, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-1732-8355
Sebastian SchölchJCCU Translational Surgical Oncology (A430), German Cancer Research Center, Heidelberg, Germany.ORCID 0000-0003-0012-3177
Stephanie S KapelEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0001-8629-2398
Nicolas GengenbacherEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0003-0642-4886
Mahak SinghalEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-7303-9585
Benjamin SchiebEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-3943-5867
Claudine FrickeEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0003-2479-176X
Rainer WillGenomics & Proteomics Core Facilities, German Cancer Research Center, Heidelberg, Germany.ORCID 0000-0001-6049-2690
Kim RemansProtein Expression and Purification Core Facility, European Molecular Biology Center, Heidelberg, Germany.ORCID 0000-0002-4394-7953
Jochen Sven UtikalDepartment of Dermatology, Venereology and Allergy, University Medical Centre Mannheim, Medical Faculty Mannheim, Heidelberg University and Centre of Excellence of Dermatology of Baden-Württemberg, Mannheim, Germany.ORCID 0000-0001-5316-0241
Christoph ReissfelderDepartment of Surgery, University Medical Centre Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0003-4591-1046
Matthias SchlesnerBiomedical Informatics, Data Mining and Data Analytics, Augsburg University, Augsburg, Germany.ORCID 0000-0002-5896-4086
Kairbaan M Hodivala-DilkeCenter for Tumor Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science Center, London, United Kingdom.ORCID 0000-0002-2859-749X
Sander KerstenNutrition, Metabolism and Genomics group, Division of Human Nutrition and Health, Wageningen University, Wageningen, The Netherlands.ORCID 0000-0003-4488-7734
Sergij GoerdtEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-5718-415X
Hellmut G Augustin *European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-7173-4242
Moritz Felcht *European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-8032-9716
German Cancer Research Center · DEHeidelberg University · DEUniversity of Augsburg · DEEuropean Molecular Biology Laboratory · DEQueen Mary University of London · GBUniversity of Basel · CHWageningen University & Research · NL

Funding

European Research Council 787181
6 · The paper itself

Abstract

Primary tumors and distant site metastases form a bidirectionally communicating system. Yet, the molecular mechanisms of this crosstalk are poorly understood. Here, we identified the proteolytically cleaved fragments of angiopoietin-like 4 (ANGPTL4) as contextually active protumorigenic and antitumorigenic contributors in this communication ecosystem. Preclinical studies in multiple tumor models revealed that the C-terminal fragment (cANGPTL4) promoted tumor growth and metastasis. In contrast, the N-terminal fragment of ANGPTL4 (nANGPTL4) inhibited metastasis and enhanced overall survival in a postsurgical metastasis model by inhibiting WNT signaling and reducing vascularity at the metastatic site. Tracing ANGPTL4 and its fragments in tumor patients detected full-length ANGPTL4 primarily in tumor tissues, whereas nANGPTL4 predominated in systemic circulation and correlated inversely with disease progression. The study highlights the spatial context of the proteolytic cleavage-dependent pro- and antitumorigenic functions of ANGPTL4 and identifies and validates nANGPTL4 as a novel biomarker of tumor progression and antimetastatic therapeutic agent.

Indexed as

Angiopoietin-Like Protein 4NeoplasmsAngiopoietinsBiomarkers, TumorHumansPeptide FragmentsAngiopoietin-Like Protein 4AngiopoietinsBiomarkers, Tumorpeptide fragment cANGPTL4peptide fragment nANGPTL4Peptide Fragments

Identifiers

PMID36269299
PMCPMC9595206
OpenAlexW4307030305

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.