Evidence map›Paper›PMID 23613996›Full record

ArticlePloS one2013

Stat3 downstream gene product chitinase 3-like 1 is a potential biomarker of inflammation-induced lung cancer in multiple mouse lung tumor models and humans.

Cong Yan, Xinchun Ding, Lingyan Wu, Menggang Yu, Peng Qu, Hong Du

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Review
  9. Article
  10. Chitinase-3-like-1/YKL-40 as marker of circulating tumor cells.Translational lung cancer research · 2015
    Review
  11. Article
  12. Article
  13. 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 at 3 institutions in 1 country.

Cong YanDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Xinchun Ding
Lingyan Wu
Menggang Yu
Peng Qu
Hong Du
Indiana University – Purdue University Indianapolis · USIndiana University Health · USUniversity of Wisconsin–Madison · US

Funding

Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI AMBER L. MOSLEY · 1999 to 2026
$59.3M
Pathophysiology of PPARgamma in the lungR01HL087001 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI DU, HONG · 2008 to 2012
$1.9M
Stat3 Downstream Genes as Lung Adenocarcinoma BiomarkersR01CA138759 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI YAN, CONG · 2010 to 2014
$1.8M
Inflammation and Immunosuppression in Lung CancerR01CA152099 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI YAN, CONG · 2011 to 2015
$1.5M
NCI NIH HHS CA138759NCI NIH HHS CA152099NCI NIH HHS P30 CA082709NCI NIH HHS R01 CA138759NCI NIH HHS R01 CA152099NHLBI NIH HHS HL087001NHLBI NIH HHS R01 HL087001
6 · The paper itself

Abstract

Over-activation of the signal transducers and activators of the transcription 3 (Stat3) pathway in lung alveolar type II (AT II) epithelial cells induces chronic inflammation and adenocarcinoma in the lung of CCSP-rtTA/(tetO)7-CMV-Stat3C bitransgenic mice. One of Stat3 downstream genes products, chitinase 3-like 1 (CHI3L1) protein, showed increased concentration in both bronchioalveolar lavage fluid (BALF) and blood of doxycycline-treated CCSP-rtTA/(tetO)7-CMV-Stat3C bitransgenic mice. When tested in other inflammation-induced lung cancer mouse models, the CHI3L1 protein concentration was also highly increased in BALF and blood of these models with tumors. Immunohistochemical staining showed strong staining of CHI3L1 protein around tumor areas in these mouse models. Analysis of normal objects and lung cancer patients revealed a significant elevation of CHI3L1 protein concentration in human serum samples from all categories of lung cancers. Furthermore, recombinant CHI3L protein stimulated proliferation and growth of Lewis lung cancer cells. Therefore, secretory CHI3L1 plays an important role in inflammation-induced lung cancer formation and potentially serve as a biomarker for lung cancer prediction. Based on our previous publication and this work, this is the first animal study linking overexpression of CHI3L1 to various lung tumor mouse models. These models will facilitate identification of additional biomarkers to predict and verify lung cancer under various pathogenic conditions, which normally cannot be done in humans.

Indexed as

AnimalsBiomarkers, TumorBronchoalveolar Lavage FluidCell Line, TumorChitinase-3-Like Protein 1Disease Models, AnimalGene Expression Regulation, NeoplasticGlycoproteinsHumansInflammationLungLung NeoplasmsMiceMice, TransgenicSTAT3 Transcription FactorBiomarkers, TumorChil1 protein, mouseChitinase-3-Like Protein 1GlycoproteinsSTAT3 Transcription Factor

Identifiers

PMID23613996
PMCPMC3632574
OpenAlexW2080823640

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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.