Evidence map›Paper›PMID 38799433›Full record

ReviewFrontiers in immunology2024

Emerging role of immunogenic cell death in cancer immunotherapy.

Kei-Ichiro Arimoto, Sayuri Miyauchi, Mengdan Liu, Dong-Er Zhang

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
–field-weighted citation impact
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

56 citing papers in PubMed.

  1. Review
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  6. Degraded sulfated galactan derived fromMolecular medicine reports · 2026
    Article
  7. European journal of nuclear medicine and molecular imaging · 2026
    Article
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  16. Probiotics Cancer Interaction, Prevention, and Therapy.Immunity, inflammation and disease · 2026
    Review
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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

4 authors.

Kei-Ichiro ArimotoMoores Cancer Center, University of California San Diego, La Jolla, CA, United States.
Sayuri MiyauchiMoores Cancer Center, University of California San Diego, La Jolla, CA, United States.
Mengdan LiuMoores Cancer Center, University of California San Diego, La Jolla, CA, United States.
Dong-Er ZhangMoores Cancer Center, University of California San Diego, La Jolla, CA, United States.

Funding

ISG15 and Protein ISGylation in CancerR01CA177305 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, DONG-ER · 2013 to 2023
$3.7M
USP18 in Cancer DevelopmentR01CA232147 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, DONG-ER · 2019 to 2023
$1.9M
NCI NIH HHS R01 CA177305NCI NIH HHS R01 CA232147
6 · The paper itself

Abstract

Cancer immunotherapy, such as immune checkpoint blockade (ICB), has emerged as a groundbreaking approach for effective cancer treatment. Despite its considerable potential, clinical studies have indicated that the current response rate to cancer immunotherapy is suboptimal, primarily attributed to low immunogenicity in certain types of malignant tumors. Immunogenic cell death (ICD) represents a form of regulated cell death (RCD) capable of enhancing tumor immunogenicity and activating tumor-specific innate and adaptive immune responses in immunocompetent hosts. Therefore, gaining a deeper understanding of ICD and its evolution is crucial for developing more effective cancer therapeutic strategies. This review focuses exclusively on both historical and recent discoveries related to ICD modes and their mechanistic insights, particularly within the context of cancer immunotherapy. Our recent findings are also highlighted, revealing a mode of ICD induction facilitated by atypical interferon (IFN)-stimulated genes (ISGs), including polo-like kinase 2 (

Indexed as

Immunogenic Cell DeathImmunotherapyNeoplasmsAnimalsHumansImmune Checkpoint InhibitorsSignal TransductionImmune Checkpoint Inhibitorsanti-tumor immune responseimmunogenic cell death (ICD)immunotherapiesinterferonPLK2tumor biologytumor micreoenvironment (TME)USP18 (UBP43)

Identifiers

PMID38799433
PMCPMC11116615

What OpenQuestion holds

Textmetadata
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.