Evidence map›Paper›PMID 33413419›Full record

ArticleMolecular cancer2021

ITGBL1 is a new immunomodulator that favors development of melanoma tumors by inhibiting natural killer cells cytotoxicity.

Yann Cheli, Meri K Tulic, Najla El Hachem, Nicolas Nottet, Arnaud Jacquel, Maeva Gesson, Thomas Strub, Karine Bille, Alexandra Picard-Gauci, Henri Montaudié and 5 more

Erratum issuedOpen access · goldAbstract readLetter
In one paragraph

Article in Molecular cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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, 19 citations in OpenAlex.

  1. Article
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  6. Emerging roles of MITF as a crucial regulator of immunity.Experimental & molecular medicine · 2024
    Review
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  12. Review
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  14. NRF2 Enables EGFR Signaling in Melanoma Cells.International journal of molecular sciences · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Yann CheliUniversité Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France. Yann.Cheli@univ-cotedazur.fr.ORCID http://orcid.org/0000-0001-9839-4332
Meri K TulicUniversité Nice Côte d'Azur, INSERM, U1065, Team12 Study of the melanocytic differentiation applied to vitiligo and melanoma, 06000, Nice, France.
Najla El HachemLaboratory of Cancer Signaling, University of Liège, Liège, Belgium.
Nicolas NottetUniversité Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Arnaud JacquelUniversité Nice Côte d'Azur, INSERM, U1065, Team2 Cell death, differentiation and cancer, 06000, Nice, France.
Maeva GessonUniversité Nice Côte d'Azur, INSERM, U1065, Imaging platform, 06000, Nice, France.
Thomas StrubUniversité Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Karine BilleUniversité Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Alexandra Picard-GauciCHU NICE, Département de Dermatologie, 06000, Nice, France.
Henri MontaudiéCHU NICE, Département de Dermatologie, 06000, Nice, France.
Guillaume E BerangerUniversité Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Thierry PasseronUniversité Nice Côte d'Azur, INSERM, U1065, Team12 Study of the melanocytic differentiation applied to vitiligo and melanoma, 06000, Nice, France.
Pierre CloseLaboratory of Cancer Signaling, University of Liège, Liège, Belgium.
Corine Bertolotto *Université Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Robert Ballotti *Université Nice Côte d'Azur, INSERM U1065, Team1 Biology and pathologies of melanocytes. Equipe labellisée ARC 2019, 06000, Nice, France.
Inserm · FRCentre Hospitalier Universitaire de Nice · FRUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistances to immunotherapies remains a major hurdle towards a cure for melanoma in numerous patients. An increase in the mesenchymal phenotype and a loss of differentiation have been clearly associated with resistance to targeted therapies. Similar phenotypes have been more recently also linked to resistance to immune checkpoint therapies. We demonstrated here that the loss of MIcrophthalmia associated Transcription Factor (MITF), a pivotal player in melanocyte differentiation, favors the escape of melanoma cells from the immune system. We identified Integrin beta-like protein 1 (ITGBL1), a secreted protein, upregulated in anti-PD1 resistant patients and in MITF

Indexed as

Cytotoxicity, ImmunologicAnimalsCarcinogenesisCell Line, TumorCell ProliferationImmunologic FactorsIntegrin beta1Killer Cells, NaturalMelanomaMiceMice, Inbred C57BLMicrophthalmia-Associated Transcription FactorImmunologic FactorsIntegrin beta1ITGBL1 protein, humanMicrophthalmia-Associated Transcription FactorITGBL1MelanomaMITF

Identifiers

PMID33413419
PMCPMC7789764
OpenAlexW3119405288

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.