Evidence map›Paper›PMID 30205617›Full record

ReviewInternational journal of molecular sciences2018

The Role of IL-33/ST2 Pathway in Tumorigenesis.

Kristen M Larsen, Maydelis Karla Minaya, Vivek Vaish, Maria Marjorette O Peña

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 3 pooled it
4.7field-weighted citation impact, top 4% 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

70 citing papers in PubMed, 3 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Targeting IL-33 in Precision Neuroimmunology: Cellular Mechanisms and Therapeutic Strategies for CNS Disorders.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Review
  6. Article
  7. Article
  8. ILC2s and their immune checkpoints in the antitumor response.Journal for immunotherapy of cancer · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Etoposide activates CD8Journal for immunotherapy of cancer · 2025
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

10 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Kristen M LarsenDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA. kmlarsen@email.sc.edu.
Maydelis Karla MinayaDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA. maydelis_minaya@brown.edu.
Vivek VaishDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA. vivekvaish@live.com.
Maria Marjorette O PeñaDepartment of Biological Sciences and Center for Colon Cancer Research, University of South Carolina, Columbia, SC 29208, USA. mpena@biol.sc.edu.
University of South Carolina · US

Funding

National Institutes of Health R01CA154731, P3GM1033336
6 · The paper itself

Abstract

Cancer is initiated by mutations in critical regulatory genes; however, its progression to malignancy is aided by non-neoplastic cells and molecules that create a permissive environment known as the tumor stroma or microenvironment (TME). Interleukin 33 (IL-33) is a dual function cytokine that also acts as a nuclear factor. IL-33 typically resides in the nucleus of the cells where it is expressed. However, upon tissue damage, necrosis, or injury, it is quickly released into extracellular space where it binds to its cognate receptor suppression of tumorigenicity 2 (ST2)L found on the membrane of target cells to potently activate a T Helper 2 (Th2) immune response, thus, it is classified as an alarmin. While its role in immunity and immune-related disorders has been extensively studied, its role in tumorigenesis is only beginning to be elucidated and has revealed opposing roles in tumor development. The IL-33/ST2 axis is emerging as a potent modulator of the TME. By recruiting a cohort of immune cells, it can remodel the TME to promote malignancy or impose tumor regression. Here, we review its multiple functions in various cancers to better understand its potential as a therapeutic target to block tumor progression or as adjuvant therapy to enhance the efficacy of anticancer immunotherapies.

Indexed as

Signal TransductionAnimalsCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHumansInterleukin-1 Receptor-Like 1 ProteinInterleukin-33NeoplasmsTumor MicroenvironmentIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33cancerIL-33/ST2 signalinginflammationInterleukin 33tumor microenvironment

Identifiers

PMID30205617
PMCPMC6164146
OpenAlexW2890938707

What Socratic 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 Socratic graph.