Evidence map›Paper›PMID 27120577›Full record

ArticleMolecular carcinogenesis2017

IL-33 promotes growth and liver metastasis of colorectal cancer in mice by remodeling the tumor microenvironment and inducing angiogenesis.

Yu Zhang, Celestia Davis, Sapana Shah, Daniel Hughes, James C Ryan, Diego Altomare, Maria Marjorette O Peña

Open access · greenAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

98 citing papers in PubMed, 150 citations in OpenAlex.

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38 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

7 authors at 2 institutions in 1 country.

Yu ZhangDepartment of Biological Sciences, University of South Carolina, Columbia, South Carolina.
Celestia DavisDepartment of Biological Sciences, University of South Carolina, Columbia, South Carolina.
Sapana ShahDepartment of Biological Sciences, University of South Carolina, Columbia, South Carolina.
Daniel HughesDepartment of Biological Sciences, University of South Carolina, Columbia, South Carolina.
James C RyanProteoGenomics, LLC, Vero Beach, Florida.
Diego AltomareCollege of Pharmacy, Drug Discovery and Biomedical Sciences, University of South Carolina, Columbia, South Carolina.
Maria Marjorette O PeñaDepartment of Biological Sciences, University of South Carolina, Columbia, South Carolina.
University of South Carolina · USInnoGenomics (United States) · US

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
TISSUE BIOREPOSITORYP20RR017698 · NCRR · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FAYAD, RAJA · 2002 to 2011
$22.5M
TISSUE BIOREPOSITORY COREP30GM103336 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI BERGER, FRANKLIN G. · 2013 to 2017
$5.4M
Stromal modulation of response to Thymidylate synthase inhibitorsR01CA154731 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PENA, MARIA MARJORETTE · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA154731NCRR NIH HHS P20 RR017698NIGMS NIH HHS P20 GM103499NIGMS NIH HHS P30 GM103336
6 · The paper itself

Abstract

Liver metastasis is the major cause of death from colorectal cancer (CRC). Understanding its mechanisms is necessary for timely diagnosis and development of effective therapies. Interleukin-33 (IL-33) is an IL-1 cytokine family member that uniquely functions as a cytokine and nuclear factor. It is released by necrotic epithelial cells and activated innate immune cells, functioning as an alarmin or an early danger signal. Its role in invoking type 2 immune response has been established; however, it has contrasting roles in tumor development and metastasis. We identified IL-33 as a potently upregulated cytokine in a highly metastatic murine CRC cell line and examined its role in tumor growth and metastasis to the liver. IL-33 was transgenically expressed in murine and human adenocarcinoma and carcinoma cell lines and their growth and spontaneous metastasis to the liver were assessed in orthotopic models of CRC in wild-type C57Bl/6 and Il33 knockout mice. The results showed that increased expression of IL-33 in CRC cells enhanced their tumor take, growth, and liver metastasis. Tumor- rather than host-derived IL-33 induced the enhanced recruitment of CD11b

Indexed as

Tumor MicroenvironmentAnimalsCell Line, TumorColonColorectal NeoplasmsGene Expression Regulation, NeoplasticHumansInterleukin-33LiverLiver NeoplasmsMaleMiceMice, Inbred BALB CMice, Inbred C57BLNeovascularization, PathologicRectumInterleukin-33alarmincolon cancercytokinesinflammationmyeloid cells

Identifiers

PMID27120577
PMCPMC5630136
OpenAlexW2372899587

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.