Evidence map›Paper›PMID 34944095›Full record

ReviewCells2021

The Functional and Mechanistic Roles of Immunoproteasome Subunits in Cancer.

Satyendra Chandra Tripathi, Disha Vedpathak, Edwin Justin Ostrin

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 30 citations in OpenAlex.

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  14. Microproteins unveiling new dimensions in cancer.Functional & integrative genomics · 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

3 authors at 2 institutions in 2 countries.

Satyendra Chandra TripathiDepartment of Biochemistry, All India Institute of Medical Sciences Nagpur, Nagpur 441108, MH, India.ORCID 0000-0003-3917-9645
Disha VedpathakDepartment of Biochemistry, All India Institute of Medical Sciences Nagpur, Nagpur 441108, MH, India.
Edwin Justin OstrinDepartment of General Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-4538-6539
All India Institute of Medical Sciences, Nagpur · INThe University of Texas MD Anderson Cancer Center · US

Funding

Science and Engineering Research Board SERB-DST-SRG/2020/001564
6 · The paper itself

Abstract

Cell-mediated immunity is driven by antigenic peptide presentation on major histocompatibility complex (MHC) molecules. Specialized proteasome complexes called immunoproteasomes process viral, bacterial, and tumor antigens for presentation on MHC class I molecules, which can induce CD8 T cells to mount effective immune responses. Immunoproteasomes are distinguished by three subunits that alter the catalytic activity of the proteasome and are inducible by inflammatory stimuli such as interferon-γ (IFN-γ). This inducible activity places them in central roles in cancer, autoimmunity, and inflammation. While accelerated proteasomal degradation is an important tumorigenic mechanism deployed by several cancers, there is some ambiguity regarding the role of immunoproteasome induction in neoplastic transformation. Understanding the mechanistic and functional relevance of the immunoproteasome provides essential insights into developing targeted therapies, including overcoming resistance to standard proteasome inhibition and immunomodulation of the tumor microenvironment. In this review, we discuss the roles of the immunoproteasome in different cancers.

Indexed as

AnimalsHumansModels, BiologicalNeoplasmsProteasome Endopeptidase ComplexProteasome InhibitorsProtein SubunitsProteasome Endopeptidase ComplexProteasome InhibitorsProtein Subunitsimmunoproteasomeproteasome inhibitorssolid tumorsubiquitin–proteasome system (UPS)

Identifiers

PMID34944095
PMCPMC8700164
OpenAlexW4200084901

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.