Evidence map›Paper›PMID 26979394›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2016

Lack of Immunomodulatory Interleukin-27 Enhances Oncogenic Properties of Mutant p53 In Vivo.

Denada Dibra, Abhisek Mitra, Melisa Newman, Xueqing Xia, Jeffry J Cutrera, Mihai Gagea, Eugenie S Kleinerman, Guillermina Lozano, Shulin Li

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  3. Inflammation suppresses DLG2 expression decreasing inflammasome formation.Journal of cancer research and clinical oncology · 2022
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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

9 authors at 2 institutions in 1 country.

Denada DibraDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Abhisek MitraDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Melisa NewmanBanfield Pet Hospital, Sugar Land, Texas.
Xueqing XiaDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jeffry J CutreraDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mihai GageaDepartment of Veterinary Medicine and Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Eugenie S KleinermanDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Guillermina LozanoDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Shulin LiDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas. sli4@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USHouston Methodist Sugar Land Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Gene-Product Auto-Targeting to Tumor VesselsR01CA120895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2007 to 2025
$4.8M
IL12 Gene Therapy For Enhancing Therapeutic Efficacy of Bleomycin Against Oral TuR01CA142855 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2010 to 2014
$1.6M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA120895NCI NIH HHS R01 CA142855
6 · The paper itself

Abstract

purposep53 is mutated in about 50% of human cancers, mostly through missense mutations. Expression of mutant p53 is associated with poor clinical outcomes or metastasis. Although mutant p53 is inherently instable, various stressors such as DNA damage or expression of the oncogenic Kras or c-myc affect the oncogenic properties of mutant p53. However, the effects of inflammation on mutant p53 are largely unknown. IL27 is an important immunomodulatory cytokine, but its impact on mutant p53-driven tumorigenesis has not been reported. EXPERIMENTAL

designIL27RA(-/-) mice were bred with mutant p53 heterozygous (p53(R172H/+)) mice to obtain IL27RA(-/-)p53(H/+) and IL27RA(-/-)p53(H/H) mice. Mouse survival and tumor spectra for the cohort were analyzed. Stability of p53 protein was analyzed via IHC and Western blot analysis.

resultsThis study unraveled that lack of IL27 signaling significantly shortened the survival duration of mice with tumors expressing both copies of the mutant p53 gene (Li-Fraumeni mouse model). Interestingly, in mice that were heterozygous for mutant p53, lack of IL27 signaling not only significantly shortened survival time but also doubled the incidence of osteosarcomas. Furthermore, lack of IL27 signaling is closely associated with increased mutant p53 stability in vivo from early age.

conclusionsThese results suggest that IL27 signaling modulates the oncogenic properties of mutant p53 in vivo Clin Cancer Res; 22(15); 3876-83. ©2016 AACR.

Indexed as

ImmunomodulationMutationAnimalsCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticDisease Models, AnimalGenotypeHeterograftsHumansImmunohistochemistryInterleukin-27MiceMice, KnockoutReceptors, InterleukinIL27RA protein, humanInterleukin-27Receptors, InterleukinTumor Suppressor Protein p53

Identifiers

PMID26979394
PMCPMC4970873
OpenAlexW2297938062

What OpenQuestion holds

Textmetadata
LicenceTDM
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.