Evidence map›Paper›PMID 32893980›Full record

ArticleThoracic cancer2020

MicroRNA-200b is a potential biomarker of the expression of PD-L1 in patients with lung cancer.

Seigo Katakura, Nobuaki Kobayashi, Hisashi Hashimoto, Chisato Kamimaki, Katsushi Tanaka, Sousuke Kubo, Kentaro Nakashima, Shuhei Teranishi, Saki Manabe, Keisuke Watanabe and 6 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

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  6. MicroRNA-200c in Cancer Generation, Invasion, and Metastasis.International journal of molecular sciences · 2025
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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

16 authors at 3 institutions in 2 countries.

Seigo KatakuraDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Nobuaki KobayashiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0002-7064-320X
Hisashi HashimotoDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Chisato KamimakiDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Katsushi TanakaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Sousuke KuboDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Kentaro NakashimaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Shuhei TeranishiRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Saki ManabeRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Keisuke WatanabeDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0001-9623-1492
Nobuyuki HoritaDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0002-8200-0340
Yu HaraDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0002-2574-2516
Masaki YamamotoRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.ORCID 0000-0001-7056-4192
Makoto KudoRespiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.
Hongmei PiaoDepartment of Respiratory Medicine, Affiliated Hospital of Yanbian University, Yanji, China.
Takeshi KanekoDepartment of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yokohama City University · JPYokohama City University Medical Center · JPYanbian University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced non-small cell lung cancer (NSCLC) has a high mortality rate and poor prognosis. However, outcomes have gradually improved after the introduction of novel immunotherapies, including immune checkpoint inhibitors (ICIs). Although programmed death-ligand 1 (PD-L1) expression in tumor tissues is a known biomarker for guiding ICI treatment of NSCLC, challenges such as difficulty of liquid biopsy and heterogeneous results during treatment persist. This study evaluated the potential of miR200b as a surrogate biomarker for PD-L1 expression.

methodsWe used the human lung cancer cell lines H226, H460, H520, A549, and H1975. miR200b expression in blood and bronchoscopy specimens of NSCLC patients was evaluated using reverse-transcription-quantitative PCR. Using flow cytometry, PD-L1 expression in vitro, as well as in tumor tissues, was evaluated after transfection with a mimic miR200b or siRNA.

resultsmiR200b expression negatively correlated with PD-L1 expression in all cell lines. The induction or knockdown of miR200b also altered PD-L1 expression in vitro. The patient group with a PD-L1 tumor proportion score ≥ 50% had significantly lower miR200b expression in the bronchoscopy specimens (P = 0.025) and serum-derived exosomes (P = 0.022) than that with PD-L1 tumor proportion score < 50%.

conclusionsmiR200b can regulate PD-L1 expression in lung cancer cells, and miR200b expression in clinical specimens negatively correlated with PD-L1 expression. Thus, miR200b may be a useful surrogate biomarker for PD-L1 expression in lung cancer patients. KEY POINTS: SIGNIFICANT FINDINGS OF THE STUDY: High PD-L1 expression was linked to low miR200b expression, whereas low PD-L1 expression was linked to high miR200b expression in human lung cancer patients. Thus, miR200b overexpression or silencing can control PD-L1 expression in cancer cells. What this study adds We demonstrated the potential of miR200b as a surrogate biomarker for PD-L1 expression in lung cancer patients.

Indexed as

AgedAged, 80 and overB7-H1 AntigenBiomarkers, TumorCell Line, TumorFemaleHumansLung NeoplasmsMaleMicroRNAsMiddle AgedB7-H1 AntigenBiomarkers, TumorCD274 protein, humanMicroRNAsMIRN200 microRNA, humanBiomarkersexosomesmiRNAnon-small cell lung cancerprogrammed cell death 1 ligand 1

Identifiers

PMID32893980
PMCPMC7529545
OpenAlexW3084418924

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LicenceCC BY
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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.