Evidence map›Paper›PMID 38009521›Full record

ArticleEMBO molecular medicine2023

Tumor endothelial cell autophagy is a key vascular-immune checkpoint in melanoma.

Jelle Verhoeven, Kathryn A Jacobs, Francesca Rizzollo, Francesca Lodi, Yichao Hua, Joanna Poźniak, Adhithya Narayanan Srinivasan, Diede Houbaert, Gautam Shankar, Sanket More and 15 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 26 citations in OpenAlex.

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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

25 authors at 6 institutions in 3 countries.

Jelle Verhoeven *Cell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0003-1534-3340
Kathryn A Jacobs *Cell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0003-3632-6400
Francesca RizzolloCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0002-5211-7281
Francesca LodiLaboratory of Translational Genetics, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0003-4321-1812
Yichao HuaLaboratory of Tumor Microenvironment and Therapeutic Resistance Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0002-1695-172X
Joanna PoźniakDepartment of Oncology, KU Leuven, Leuven, Belgium.
Adhithya Narayanan SrinivasanCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.
Diede HoubaertCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.
Gautam ShankarLaboratory of Translational Cell and Tissue Research, Department of Pathology, KULeuven and UZ Leuven, Leuven, Belgium.
Sanket MoreCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0003-3482-4414
Marco B SchaafCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.
Nikolina Dubroja LakicLaboratory of Translational Cell and Tissue Research, Department of Pathology, KULeuven and UZ Leuven, Leuven, Belgium.
Maarten GanneCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.
Jochen LamoteDepartment of Oncology, KU Leuven, Leuven, Belgium.
Johan Van WeyenberghLaboratory of Clinical and Epidemiological Virology, Department of Microbiology, Immunology and Transplantation, Rega Institute for Medical Research, KU Leuven, Leuven, Belgium.
Louis BoonPolpharma Biologics, Utrecht, The Netherlands.
Oliver BechterDepartment of General Medical Oncology, UZ Leuven, Leuven, Belgium.ORCID 0000-0003-0667-3284
Francesca BosisioLaboratory of Translational Cell and Tissue Research, Department of Pathology, KULeuven and UZ Leuven, Leuven, Belgium.
Yasuo UchiyamaDepartment of Cellular and Molecular Neuropathology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Mathieu Jm BertrandVIB Center for Inflammation Research, Ghent University, Ghent, Belgium.
Jean Christophe MarineLaboratory for Molecular Cancer Biology, Center for Cancer Biology, VIB, Leuven, Belgium.
Diether LambrechtsLaboratory of Translational Genetics, Center for Cancer Biology, VIB, Leuven, Belgium.
Gabriele BergersLaboratory of Tumor Microenvironment and Therapeutic Resistance Center for Cancer Biology, VIB, Leuven, Belgium.
Madhur AgrawalCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0002-0966-8571
Patrizia AgostinisCell Death Research and Therapy Laboratory, Center for Cancer Biology, VIB, Leuven, Belgium.ORCID 0000-0003-1314-2115
VIB-KU Leuven Center for Cancer Biology · BEUniversitair Ziekenhuis Leuven · BEGhent University · BEJuntendo University · JPPolpharma Biologics (Netherlands) · NLRega Institute for Medical Research · BE

Funding

EOS CD-INFLADISEOS DECODE 30837538EOS MetaNiche 40007532Fonds Wetenschappelijk Onderzoek (FWO) 1155121NFonds Wetenschappelijk Onderzoek (FWO) 11L7622NFonds Wetenschappelijk Onderzoek (FWO) 12Y4322NFonds Wetenschappelijk Onderzoek (FWO) G035320NFonds Wetenschappelijk Onderzoek (FWO) G044518NFonds Wetenschappelijk Onderzoek (FWO) G049817NFonds Wetenschappelijk Onderzoek (FWO) G070115NFonds Wetenschappelijk Onderzoek (FWO) G076617NiBOF-Atlantis iBOF/21/053Stichting Tegen Kanker (Fondation Contre le Cancer) FAF-F/2018/1252UGhent BOF23/GOA/001
6 · The paper itself

Abstract

Tumor endothelial cells (TECs) actively repress inflammatory responses and maintain an immune-excluded tumor phenotype. However, the molecular mechanisms that sustain TEC-mediated immunosuppression remain largely elusive. Here, we show that autophagy ablation in TECs boosts antitumor immunity by supporting infiltration and effector function of T-cells, thereby restricting melanoma growth. In melanoma-bearing mice, loss of TEC autophagy leads to the transcriptional expression of an immunostimulatory/inflammatory TEC phenotype driven by heightened NF-kB and STING signaling. In line, single-cell transcriptomic datasets from melanoma patients disclose an enriched Inflammatory

Indexed as

MelanomaAnimalsAutophagyCD8-Positive T-LymphocytesEndothelial CellsHumansImmunotherapyMiceNF-kappa BTumor MicroenvironmentNF-kappa Bautophagycancerimmunotherapyinflammationtumor endothelial cells

Identifiers

PMID38009521
PMCPMC10701618
OpenAlexW4389037422

What OpenQuestion holds

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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.