Evidence map›Paper›PMID 33956406›Full record

ArticleEMBO molecular medicine2021

CXCR4 engagement triggers CD47 internalization and antitumor immunization in a mouse model of mesothelioma.

Rosanna Mezzapelle, Francesco De Marchis, Chiara Passera, Manuela Leo, Francesca Brambilla, Federica Colombo, Maura Casalgrandi, Alessandro Preti, Samuel Zambrano, Patrizia Castellani and 14 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% 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, 22 citations in OpenAlex.

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  5. Increased PRP19 in Hepatocyte Impedes B Cell Function to Promote Hepatocarcinogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 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

24 authors at 6 institutions in 1 country.

Rosanna MezzapelleChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Francesco De MarchisChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID 0000-0003-1275-5470
Chiara PasseraChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Manuela LeoDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Francesca BrambillaChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Federica ColomboChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Maura CasalgrandiHMGBiotech S.r.l., Milan, Italy.
Alessandro PretiHMGBiotech S.r.l., Milan, Italy.
Samuel ZambranoChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Patrizia CastellaniCell Biology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.ORCID 0000-0002-6326-5853
Riccardo ErtassiChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Marco SilingardiSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Francesca CaprioglioSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Veronica BassoDivision of Immunology, Transplantation and Infectious Diseases, Lymphocyte Activation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Renzo BoldoriniDepartment of Health Science, School of Medicine, University of Eastern Piedmont Amedeo Avogadro, Vercelli, Italy.
Angelo CarrettaDepartment of Thoracic Surgery, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Francesca SanvitoDepartment of Pathology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Ottavio RenaUnit of Thoracic Surgery, Maggiore della Carità Hospital, Novara, Italy.
Anna RubartelliCell Biology Unit, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Lina SabatinoDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Anna MondinoDivision of Immunology, Transplantation and Infectious Diseases, Lymphocyte Activation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Massimo P CrippaChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Vittorio ColantuoniDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Marco E BianchiChromatin Dynamics Unit, Division of Genetics and Cell Biology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Vita-Salute San Raffaele University · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Sannio · ITOspedale Policlinico San Martino · ITAzienda Ospedaliera Ospedale Maggiore · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Boosting antitumor immunity has emerged as a powerful strategy in cancer treatment. While releasing T-cell brakes has received most attention, tumor recognition by T cells is a pre-requisite. Radiotherapy and certain cytotoxic drugs induce the release of damage-associated molecular patterns, which promote tumor antigen cross-presentation and T-cell priming. Antibodies against the "do not eat me" signal CD47 cause macrophage phagocytosis of live tumor cells and drive the emergence of antitumor T cells. Here we show that CXCR4 activation, so far associated only with tumor progression and metastasis, also flags tumor cells to immune recognition. Both CXCL12, the natural CXCR4 ligand, and BoxA, a fragment of HMGB1, promote the release of DAMPs and the internalization of CD47, leading to protective antitumor immunity. We designate as Immunogenic Surrender the process by which CXCR4 turns in tumor cells to macrophages, thereby subjecting a rapidly growing tissue to immunological scrutiny. Importantly, while CXCL12 promotes tumor cell proliferation, BoxA reduces it, and might be exploited for the treatment of malignant mesothelioma and a variety of other tumors.

Indexed as

CD47 AntigenMesotheliomaAnimalsCell Line, TumorImmunizationMacrophagesMicePhagocytosisCD47 AntigenCD47CXCR4HMGB1immunogenic cell deathmesothelioma

Identifiers

PMID33956406
PMCPMC8185548
OpenAlexW3158846671

What OpenQuestion holds

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LicenceCC BY
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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.