Evidence map›Paper›PMID 39079535›Full record

ArticleImmunity2024

Cancer stem cells release interleukin-33 within large oncosomes to promote immunosuppressive differentiation of macrophage precursors.

Hannah L Erickson, Sachiko Taniguchi, Anish Raman, Justin J Leitenberger, Sanjay V Malhotra, Naoki Oshimori

Abstract read
In one paragraph

Article in Immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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  13. Etoposide activates CD8Journal for immunotherapy of cancer · 2025
    Article
  14. Review
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  16. Mouse TThe Journal of allergy and clinical immunology · 2025
    Article
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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

6 authors.

Hannah L EricksonDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR 97239, USA.
Sachiko TaniguchiDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR 97239, USA.
Anish RamanDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR 97239, USA.
Justin J LeitenbergerDepartment of Dermatology, Oregon Health and Science University, Portland, OR 97239, USA.
Sanjay V MalhotraDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR 97239, USA; Center for Experimental Therapeutics, Oregon Health and Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.
Naoki OshimoriDepartment of Cell, Developmental & Cancer Biology, Oregon Health and Science University, Portland, OR 97239, USA; Department of Dermatology, Oregon Health and Science University, Portland, OR 97239, USA; Department of Otolaryngology, Head & Neck Surgery, Oregon Health and Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA. Electronic address: oshimori@ohsu.edu.

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Grace B Gill · 1997 to 2026
$60.5M
Mechanisms of cellular crosstalk in tumor-promoting niche formationR01CA245535 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI OSHIMORI, NAOKI · 2021 to 2025
$2.1M
NCI NIH HHS P30 CA069533NCI NIH HHS R01 CA245535
6 · The paper itself

Abstract

In squamous cell carcinoma (SCC), macrophages responding to interleukin (IL)-33 create a TGF-β-rich stromal niche that maintains cancer stem cells (CSCs), which evade chemotherapy-induced apoptosis in part via activation of the NRF2 antioxidant program. Here, we examined how IL-33 derived from CSCs facilitates the development of an immunosuppressive microenvironment. CSCs with high NRF2 activity redistributed nuclear IL-33 to the cytoplasm and released IL-33 as cargo of large oncosomes (LOs). Mechanistically, NRF2 increased the expression of the lipid scramblase ATG9B, which exposed an "eat me" signal on the LO surface, leading to annexin A1 (ANXA1) loading. These LOs promoted the differentiation of AXNA1 receptor

Indexed as

Cell DifferentiationInterleukin-33MacrophagesNeoplastic Stem CellsAnimalsAutophagy-Related ProteinsCarcinoma, Squamous CellCell Line, TumorHumansMiceMice, Inbred C57BLTumor MicroenvironmentAutophagy-Related ProteinsInterleukin-33annexin A1ATG9bcancer stem cell nichecancer stem cellsFPR2IL-33large oncosomesmacrophagessquamous cell carcinomatumor microenvironment

Identifiers

PMID39079535
PMCPMC11324407

What OpenQuestion holds

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Registered trials

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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.