Evidence map›Paper›PMID 29348685›Full record

ArticleScientific reports2018

Overexpression of adhesion molecules and barrier molecules is associated with differential infiltration of immune cells in non-small cell lung cancer.

Young Kwang Chae, Wooyoung M Choi, William H Bae, Jonathan Anker, Andrew A Davis, Sarita Agte, Wade T Iams, Marcelo Cruz, Maria Matsangou, Francis J Giles

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Targeting Oxidative and Immune Dysregulation in Wound Healing via Gold Nanoparticle Conjugate Chitosan.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  14. Barriers to immune cell infiltration in tumors.Journal for immunotherapy of cancer · 2023
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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

10 authors at 1 institution in 1 country.

Young Kwang ChaeRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, 60611, USA. young.chae@northwestern.edu.
Wooyoung M ChoiNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
William H BaeNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
Jonathan AnkerNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
Andrew A DavisNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
Sarita AgteRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, 60611, USA.
Wade T IamsNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
Marcelo CruzNorthwestern University Feinberg School of Medicine, Chicago, 60611, USA.
Maria MatsangouRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, 60611, USA.
Francis J GilesRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, 60611, USA.
Northwestern University · US

Funding

Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
NCI NIH HHS K12 CA090625
6 · The paper itself

Abstract

Immunotherapy is emerging as a promising option for lung cancer treatment. Various endothelial adhesion molecules, such as integrin and selectin, as well as various cellular barrier molecules such as desmosome and tight junctions, regulate T-cell infiltration in the tumor microenvironment. However, little is known regarding how these molecules affect immune cells in patients with lung cancer. We demonstrated for the first time that overexpression of endothelial adhesion molecules and cellular barrier molecule genes was linked to differential infiltration of particular immune cells in non-small cell lung cancer. Overexpression of endothelial adhesion molecule genes is associated with significantly lower infiltration of activated CD4 and CD8 T-cells, but higher infiltration of activated B-cells and regulatory T-cells. In contrast, overexpression of desmosome genes was correlated with significantly higher infiltration of activated CD4 and CD8 T-cells, but lower infiltration of activated B-cells and regulatory T-cells in lung adenocarcinoma. This inverse relation of immune cells aligns with previous studies of tumor-infiltrating B-cells inhibiting T-cell activation. Although overexpression of endothelial adhesion molecule or cellular barrier molecule genes alone was not predictive of overall survival in our sample, these genetic signatures may serve as biomarkers of immune exclusion, or resistance to T-cell mediated immunotherapy.

Indexed as

Gene ExpressionBiomarkersB-LymphocytesCarcinoma, Non-Small-Cell LungCell Adhesion MoleculesDesmosomesGene Expression ProfilingHumansLung NeoplasmsLymphocyte ActivationLymphocytes, Tumor-InfiltratingModels, BiologicalT-LymphocytesTumor MicroenvironmentBiomarkersCell Adhesion Molecules

Identifiers

PMID29348685
PMCPMC5773521
OpenAlexW2783378204

What OpenQuestion 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 OpenQuestion graph.