Evidence map›Paper›PMID 28483607›Full record

ArticleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer2017

Interleukin-17A Promotes Lung Tumor Progression through Neutrophil Attraction to Tumor Sites and Mediating Resistance to PD-1 Blockade.

Esra A Akbay, Shohei Koyama, Yan Liu, Ruben Dries, Lauren E Bufe, Michael Silkes, Md Maksudul Alam, Dillon M Magee, Robert Jones, Masahisa Jinushi and 14 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06974097 (Tumor Associated Neutrophils as a Biomarker of Chemo-immunotherapy Response in Locally Advanced Non-small Cell Lung Cancer), which is not on this map. Cited by 137 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 2 pooled it
7.9field-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.

NCT06974097 not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Tumor Associated Neutrophils as a Biomarker of Chemo-immunotherapy Response in Locally Advanced Non-small Cell Lung Cancer : a Model Based on Neoadjuvant Strategy

TypeobservationalSponsorUniversity Hospital, MontpellierRan2025 to 2028Enrolled72ConditionsNon-Small Cell Lung CancerArmsblood sampling
3 · Its place in the literature

Who cites it

137 citing papers in PubMed, 2 syntheses or guidelines pooled it, 193 citations in OpenAlex.

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  18. Emerging new immune checkpoint inhibitors in solid tumor immunotherapy.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
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  20. Article

77 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

24 authors at 10 institutions in 3 countries.

Esra A AkbayDepartment of Pathology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas; Simmons Comprehensive Cancer Center, Dallas, Texas.
Shohei KoyamaDepartment of Respiratory Medicine, Allergy, and Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Yan LiuDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Ruben DriesDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Lauren E BufeDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Michael SilkesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Md Maksudul AlamDepartment of Pathology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas; Simmons Comprehensive Cancer Center, Dallas, Texas.
Dillon M MageeDepartment of Pathology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas; Simmons Comprehensive Cancer Center, Dallas, Texas.
Robert JonesBelfer Center for Applied Cancer Science, Dana-Farber Cancer Institute, Boston, Massachusetts.
Masahisa JinushiGraduate School of Medicine, Institute for Advanced Medical Research, Keio University, Tokyo, Japan.
Meghana KulkarniDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Julian CarreteroDepartment of Physiology, University of Valencia, Valencia, Spain.
Xiaoen WangDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Tiquella Warner-HattenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Jillian D CavanaughDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Akio OsaDepartment of Respiratory Medicine, Allergy, and Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Atsushi KumanogohDepartment of Respiratory Medicine, Allergy, and Rheumatic Disease, Osaka University Graduate School of Medicine, Osaka, Japan.
Gordon J FreemanDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Mark M AwadDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
David C ChristianiHarvard T.H. Chan School of Public Health, Boston, Massachusetts.
Raphael BuenoThoracic Surgery, Brigham and Women's Hospital, Boston, Massachusetts.
Peter S HammermanDepartment of Medicine, Harvard Medical School, Boston, Massachusetts; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Glenn DranoffNovartis Institutes for Biomedical Research, Cambridge, Massachusetts.
Kwok-Kin WongLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York. Electronic address: kwok-kin.wong@nyumc.org.
Dana-Farber Cancer Institute · USHarvard University · USOsaka University · JPHarold C. Simmons Comprehensive Cancer CenterBoston Biomedical Research Institute · USBrigham and Women's Hospital · USKeio University · JPNYU Langone Health · USThe University of Texas Southwestern Medical Center · USUniversitat de València · ES

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Wanling Xie · 2003 to 2026
$53.4M
Tuberous Sclerosis-Pathway and PathogenesisP01CA120964 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI David J. Kwiatkowski · 2007 to 2026
$35.9M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
MUC1-C Oncoprotein Evades Immune Destruction in Non-small Cell Lung CancerR01CA166480 · NCI · DANA-FARBER CANCER INST · PI KUFE, DONALD W., WONG, KWOK KIN · 2012 to 2021
$6.3M
Therapeutic strategies for specific subsets of KRAS mutant lung cancersR01CA140594 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WONG, KWOK KIN · 2009 to 2017
$4.5M
Therapeutic approaches for LKB1-deficient non-small cell lung cancerR01CA205150 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEYMACH, JOHN V., WONG, KWOK KIN · 2016 to 2020
$3.0M
In vivo analysis of EGFR mutant driven lung cancers responses to radiation therapR01CA122794 · NCI · DANA-FARBER CANCER INST · PI WONG, KWOK KIN · 2006 to 2015
$2.8M
In vivo murine models of metastasis for therapeutic testingR01CA163896 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHARPLESS, NORMAN E, WONG, KWOK KIN · 2012 to 2016
$2.0M
Credentialing Mouse Models for Immune System Therapy ResearchR01CA195740 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEROU, CHARLES M, WONG, KWOK KIN · 2015 to 2017
$1.8M
NCI NIH HHS P01 CA120964NCI NIH HHS P50 CA101942NCI NIH HHS R01 CA122794NCI NIH HHS R01 CA140594NCI NIH HHS R01 CA163896NCI NIH HHS R01 CA166480NCI NIH HHS R01 CA195740NCI NIH HHS R01 CA205150NCI NIH HHS R35 CA197449
6 · The paper itself

Abstract

introductionProinflammatory cytokine interleukin-17A (IL-17A) is overexpressed in a subset of patients with lung cancer. We hypothesized that IL-17A promotes a protumorigenic inflammatory phenotype and inhibits antitumor immune responses.

methodsWe generated bitransgenic mice expressing a conditional IL-17A allele along with conditional Kras

resultsTumors in IL-17:Kras

conclusionsHere we have shown that an increase in a single cytokine, IL-17A, without additional mutations can promote lung cancer growth by promoting inflammation, which contributes to resistance to PD-1 blockade and sensitizes tumors to cytokine and neutrophil depletion.

Indexed as

AnimalsDisease ProgressionGene ExpressionHumansInterleukin-17Lung NeoplasmsMiceMice, TransgenicMutationNeutrophilsProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins p21(ras)Interleukin-17Programmed Cell Death 1 ReceptorProto-Oncogene Proteins p21(ras)CytokinesIL-17MDSCNeutrophilsPD-1Resistance

Identifiers

PMID28483607
PMCPMC5532066
OpenAlexW2610919492

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.