Evidence map›Paper›PMID 28878242›Full record

ArticleScientific reports2017

Increased PD-L1 expression and IL-6 secretion characterize human lung tumor-derived perivascular-like cells that promote vascular leakage in a perfusable microvasculature model.

Colette A Bichsel, Limei Wang, Laurène Froment, Sabina Berezowska, Stefan Müller, Patrick Dorn, Thomas M Marti, Ren-Wang Peng, Thomas Geiser, Ralph A Schmid and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

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  6. Advancements in preclinical human-relevant modeling of pulmonary vasculature on-chip.European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences · 2024
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  15. Tumor Dormancy: Implications for Invasion and Metastasis.International journal of molecular sciences · 2021
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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

12 authors at 1 institution in 2 countries.

Colette A BichselARTORG Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.
Limei WangDepartment of BioMedical Research, University of Bern, Bern, Switzerland.
Laurène FromentDepartment of BioMedical Research, University of Bern, Bern, Switzerland.
Sabina BerezowskaDepartment of Pathology, University of Bern, Bern, Switzerland.ORCID 0000-0001-5442-9791
Stefan MüllerFlow cytometry core facility, Department of BioMedical Research, University of Bern, Bern, Switzerland.
Patrick DornDepartment of BioMedical Research, University of Bern, Bern, Switzerland.
Thomas M MartiDepartment of BioMedical Research, University of Bern, Bern, Switzerland.
Ren-Wang PengDepartment of BioMedical Research, University of Bern, Bern, Switzerland.
Thomas GeiserDepartment of Pulmonary Medicine, Inselspital, Bern University Hospital, Bern, Switzerland.
Ralph A SchmidDepartment of BioMedical Research, University of Bern, Bern, Switzerland. Ralph.Schmid@insel.ch.
Olivier T GuenatARTORG Organs-on-Chip Technologies, University of Bern, Bern, Switzerland.ORCID 0000-0003-1103-9712
Sean R R HallDepartment of BioMedical Research, University of Bern, Bern, Switzerland. Sean.Hall@insel.ch.ORCID 0000-0003-3561-7329
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pericytes represent important support cells surrounding microvessels found in solid organs. Emerging evidence points to their involvement in tumor progression and metastasis. Although reported to be present in the human lung, their specific presence and functional orientation within the tumor microenvironment in non-small cell lung cancer (NSCLC) has not yet been adequately studied. Using a multiparameter approach, we prospectively identified, sorted and expanded mesenchymal cells from human primary NSCLC samples based on co-expression of CD73 and CD90 while lacking hematopoietic and endothelial lineage markers (CD45, CD31, CD14 and Gly-A) and the epithelial marker EpCAM. Compared to their normal counterpart, tumor-derived Lineage-EpCAM-CD73+CD90+ cells showed enhanced expression of the immunosuppressive ligand PD-L1, a higher constitutive secretion of IL-6 and increased basal αSMA levels. In an in vitro model of 3D microvessels, both tumor-derived and matched normal Lineage-EpCAM-CD73+CD90+ cells supported the assembly of perfusable vessels. However, tumor-derived Lineage-EpCAM-CD73+CD90+ cells led to the formation of vessels with significantly increased permeability. Together, our data show that perivascular-like cells present in NSCLC retain functional abnormalities in vitro. Perivascular-like cells as an eventual target in NSCLC warrants further investigation.

Indexed as

Capillary Permeability5'-NucleotidaseB7-H1 AntigenBiomarkersCarcinoma, Non-Small-Cell LungEpithelial Cell Adhesion MoleculeHumansInterleukin-6Lung NeoplasmsMesenchymal Stem CellsMicrovesselsNeovascularization, PathologicPericytesStromal CellsThy-1 AntigensTransforming Growth Factor beta5'-NucleotidaseB7-H1 AntigenBiomarkersCD274 protein, humanEpithelial Cell Adhesion MoleculeInterleukin-6Thy-1 AntigensTransforming Growth Factor beta

Identifiers

PMID28878242
PMCPMC5587684
OpenAlexW2751663880

What OpenQuestion holds

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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.