Evidence map›Paper›PMID 34254261›Full record

ArticleSleep & breathing = Schlaf & Atmung2022

Extracellular vesicles derived from lung cancer cells exposed to intermittent hypoxia upregulate programmed death ligand 1 expression in macrophages.

Yuanling Liu, Minzhen Lu, Jianan Chen, Siqi Li, Yiyu Deng, Shifang Yang, Qiong Ou, Jing Li, Ping Gao, Zeru Luo and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Sleep & breathing = Schlaf & Atmung, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Yuanling LiuThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Minzhen LuThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Jianan ChenDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Siqi LiThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China.
Yiyu DengDepartment of Critical Care and Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, China.
Shifang YangDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Qiong OuDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Jing LiDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Ping GaoDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Zeru LuoDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Ping YuanDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Jianlong TanDepartment of Pulmonary and Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Zhongshan 2nd road No. 106, Guangzhou, 510080, China.
Xinglin GaoThe Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China. xinglingao@hotmail.com.
Guangdong Provincial People's Hospital · CNGuangdong Academy of Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIntermittent hypoxia (IH), a hallmark of obstructive sleep apnea (OSA), compromises immune surveillance through the upregulation of programmed cell death-1 ligand (PD-L1). Tumor-released extracellular vesicles (EVs) have been reported to modulate immunosuppressive activities. We investigated whether or not EVs derived from intermittent hypoxic lung cancer cells can alter the expression of PD-L1 in macrophages.

methodsThe expression of PD-L1

resultsPD-L1

conclusionIH can enhance the function of EVs derived from lung cancer cells to aggravate immunosuppressive status in macrophages. HIF-1α may play an important role in this process.

Indexed as

Carcinoma, Non-Small-Cell LungExtracellular VesiclesLung NeoplasmsSleep Apnea, ObstructiveB7-H1 AntigenHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitMacrophagesB7-H1 AntigenHypoxia-Inducible Factor 1, alpha SubunitExtracellular vesicleMacrophageNon-small-cell lung cancerObstructive sleep apneaProgrammed cell death-1 ligand

Identifiers

PMID34254261
PMCPMC9130183
OpenAlexW3181246723

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.