Evidence map›Paper›PMID 31844419›Full record

ArticleCellular & molecular biology letters2019

MiR-214 prevents the progression of diffuse large B-cell lymphoma by targeting PD-L1.

Jing-Ran Sun, Xiao Zhang, Ya Zhang

Open access · goldAbstract read
In one paragraph

Article in Cellular & molecular biology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 54 citations in OpenAlex.

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  8. Tumor immune checkpoints and their associated inhibitors.Journal of Zhejiang University. Science. B · 2022
    Review
  9. The Features of Immune Checkpoint Gene Regulation by microRNA in Cancer.International journal of molecular sciences · 2022
    Review
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  18. Regulatory mechanisms of immune checkpoints PD-L1 and CTLA-4 in cancer.Journal of experimental & clinical cancer research : CR · 2021
    Review
  19. Review
  20. Review
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

3 authors at 2 institutions in 1 country.

Jing-Ran SunLiaocheng Central Blood Station, 75 Huashan Road, Liaocheng, Shandong 25200 People's Republic of China.
Xiao Zhang2Department of Clinical Laboratory, Liaocheng People's Hospital, 67 Dongchang West Road, Liaocheng, Shandong 25200 People's Republic of China.
Ya Zhang3Department of Gynecology and Obstetrics, Liaocheng People's Hospital, 67 Dongchang West Road, Liaocheng, Shandong 25200 People's Republic of China.
Liaocheng People's Hospital · CNYancheng Central Blood Station · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe explored the role and mechanism of miR-214 involvement in the progression of diffuse large B-cell lymphoma (DLBCL).

methodsThe expression levels of miR-214 and PD-L1 in human DLBCL cell lines and in tissue samples from patients with DLBCL were determined using quantitative RT-PCR. The dual-luciferase reporter assay was employed to determine the correlation between the expressions of miR-214 and PD-L1. Cell viability, invasiveness and apoptosis were respectively examined in cells of the DLBCL line OCI-Ly3 using CCK-8, transwell and flow cytometry assays. The expression level of PD-L1 was determined via immunoblotting. Inflammatory cytokine secretion was determined via enzyme-linked immune sorbent assay (ELISA).

resultsmiR-214 was downregulated and PD-L1 was upregulated in DLBCL tissues and cell lines in comparison to normal adjacent tissues or normal B-cell. This indicates a negative correlation in the expression levels. Overexpression of miR-214 inhibited cell viability and invasion and induced apoptosis of OCI-Ly3 cells. Moreover, miR-214 was shown to target PD-L1 mRNA by binding to its 3'-untranslated region (UTR). Knockdown of PD-L1 attenuated the malignant phenotype of OCI-Ly3 cells. Overexpression of miR-214 inhibited tumor growth by targeting PD-L1 in vivo.

conclusionBy targeting PD-L1, miR-214 regulates the progression of DLBCL in vitro and in vivo.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsAgedAnimalsApoptosisB7-H1 AntigenBase PairingBase SequenceCell Line, TumorCell MovementCell SurvivalDisease ProgressionFemaleGenes, ReporterHumansLuciferases3' Untranslated RegionsB7-H1 AntigenCD274 protein, humanLuciferasesMicroRNAsMIRN214 microRNA, humanDiffuse large B-cell lymphomaInvasionmiR-214PD-L1ProliferationT cells

Identifiers

PMID31844419
PMCPMC6894298
OpenAlexW2994392690

What OpenQuestion holds

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LicenceCC BY
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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.