Evidence map›Paper›PMID 33707310›Full record

ArticleCancer immunology research2021

Pro- and Antitumorigenic Capacity of Immunoproteasomes in Shaping the Tumor Microenvironment.

Hanna Leister, Maik Luu, Daniel Staudenraus, Aleksandra Lopez Krol, Hans-Joachim Mollenkopf, Arjun Sharma, Nils Schmerer, Leon N Schulte, Wilhelm Bertrams, Bernd Schmeck and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-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

21 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Adaptation of the Tumor Antigen Presentation Machinery to Ionizing Radiation.Journal of immunology (Baltimore, Md. : 1950) · 2023
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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

13 authors at 3 institutions in 2 countries.

Hanna Leister *Institute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany.
Maik Luu *Institute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany.
Daniel StaudenrausInstitute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany.ORCID 0000-0001-5523-5681
Aleksandra Lopez KrolInstitute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany.
Hans-Joachim MollenkopfMax Planck Institute for Infection Biology, Core Facility Microarray/Genomics, Berlin, Germany.ORCID 0000-0003-1167-4783
Arjun SharmaPulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0002-5705-5470
Nils SchmererInstitute for Lung Research, UGMLC, Philipps-University Marburg, Marburg, Germany.
Leon N SchulteInstitute for Lung Research, UGMLC, Philipps-University Marburg, Marburg, Germany.ORCID 0000-0001-6814-9344
Wilhelm BertramsInstitute for Lung Research, UGMLC, Philipps-University Marburg, Marburg, Germany.ORCID 0000-0002-0180-2529
Bernd SchmeckInstitute for Lung Research, UGMLC, Philipps-University Marburg, Marburg, Germany.
Markus BosmannPulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.ORCID 0000-0003-2773-1033
Ulrich SteinhoffInstitute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany.
Alexander VisekrunaInstitute for Medical Microbiology and Hygiene, Philipps-University Marburg, Marburg, Germany. alexander.visekruna@staff.uni-marburg.de.
Philipps University of Marburg · DEBoston University · USMax Planck Institute for Infection Biology · DE

Funding

Role reversal of MAVS in bacterial sepsisR01HL141513 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOSMANN, MARKUS · 2018 to 2022
$2.4M
New genetic models for C5a receptorsR01HL139641 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOSMANN, MARKUS · 2018 to 2022
$2.1M
NHLBI NIH HHS R01 HL139641NHLBI NIH HHS R01 HL141513
6 · The paper itself

Abstract

Apart from the constitutive proteasome, the immunoproteasome that comprises the three proteolytic subunits LMP2, MECL-1, and LMP7 is expressed in most immune cells. In this study, we describe opposing roles for immunoproteasomes in regulating the tumor microenvironment (TME). During chronic inflammation, immunoproteasomes modulated the expression of protumorigenic cytokines and chemokines and enhanced infiltration of innate immune cells, thus triggering the onset of colitis-associated carcinogenesis (CAC) in wild-type mice. Consequently, immunoproteasome-deficient animals (LMP2/MECL-1/LMP7-null mice) were almost completely resistant to CAC development. In patients with ulcerative colitis with high risk for CAC, immunoproteasome-induced protumorigenic mediators were upregulated. In melanoma tumors, the role of immunoproteasomes is relatively unknown. We found that high expression of immunoproteasomes in human melanoma was associated with better prognosis. Similarly, our data revealed that the immunoproteasome has antitumorigenic activity in a mouse model of melanoma. The antitumor immunity against melanoma was compromised in immunoproteasome-deficient mice because of the impaired activity of CD8

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorColitisCysteine EndopeptidasesCytokinesFemaleHistocompatibility Antigens Class IHumansMelanoma, ExperimentalMiceMice, Inbred C57BLMice, KnockoutProteasome Endopeptidase ComplexT-Lymphocytes, CytotoxicTumor MicroenvironmentAntineoplastic AgentsCysteine EndopeptidasesCytokinesHistocompatibility Antigens Class ILMP-2 proteinLMP7 proteinProteasome Endopeptidase Complex

Identifiers

PMID33707310
PMCPMC8355016
OpenAlexW3135738346

What OpenQuestion holds

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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.