Evidence map›Paper›PMID 32891166›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

LncRNA PSMB8-AS1 contributes to pancreatic cancer progression via modulating miR-382-3p/STAT1/PD-L1 axis.

Hao Zhang, Changhao Zhu, Zhiwei He, Shiyu Chen, Lin Li, Chengyi Sun

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% 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

99 citing papers in PubMed, 1 synthesis or guideline pooled it, 185 citations in OpenAlex.

  1. Necroptosis in pancreatic cancer: Molecular mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2026
    Pooled it
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  5. Role of eRNAs in Cardiovascular Diseases.Current cardiology reviews · 2026
    Review
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39 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Hao ZhangCollege of Basic Medicine, Guizhou Medical University, Guiyang, China.
Changhao ZhuCollege of Basic Medicine, Guizhou Medical University, Guiyang, China.
Zhiwei HeCollege of Basic Medicine, Guizhou Medical University, Guiyang, China.
Shiyu ChenCollege of Basic Medicine, Guizhou Medical University, Guiyang, China.
Lin LiCollege of Basic Medicine, Guizhou Medical University, Guiyang, China.
Chengyi SunCollege of Basic Medicine, Guizhou Medical University, Guiyang, China. sunchengyi2014@163.com.
Guiyang Medical University · CN

Funding

National Natural Science Foundation of China 81860505
6 · The paper itself

Abstract

backgroundAccumulating evidence demonstrates the essential role of long non-coding RNA (lncRNA) in various types of cancers, including pancreatic cancer. However, the functions and regulation mechanism of lncRNA PMSB8-AS1 in pancreatic cancer are largely unclear.

methodsQuantitative reverse transcription PCR (qRT-PCR) is used to examine the expression of PMSB8-AS1 in PC tissues and PC cell lines. The effect of PMSB8-AS1 on the proliferation of PC cells was detected using CCK8 assay, colony assay, and flow cytometry. The effect of PMSB8-AS1 on the migration and invasion of pancreatic cancer cells was detected using a wound-healing assay and transwell migration assay. Bioinformatic analysis, double luciferase reporting assay, western blot, and rescue experiments were used to detect the regulatory relationship between PMSB8-AS1, miR-382-3p, STAT1, and PD-L1.

resultsPMSB8-AS1 expression was upregulated in PC tissues and cell lines and positively associated with the worst survival in patients with PC. The in vitro and in vivo assays demonstrated that overexpression of PMSB8-AS1 significantly promoted pancreatic cancer cell proliferation, migration, and invasion, whereas knockdown of PMSB8-AS1 suppressed cell proliferation, migration, invasion, and EMT, and decreased apoptosis of PC cells. Besides, PMSB8-AS1 directly bound to miR-382-3p downregulated its expression. Besides, PMSB8-AS1 reversed the effect of miR-382-3p on the growth and metastasis of PC cells, which might be targeted on STAT1. Furthermore, STAT1 is the transcriptional factor that activates the expression of PD-L1.

conclusionlncRNA PMSB8-AS1 promotes pancreatic cancer progression via STAT1 by sponging miR-382-3p involving regulation PD-L1.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisB7-H1 AntigenBiomarkers, TumorCell ProliferationFemaleHumansLiver NeoplasmsMiceMice, Inbred BALB CMice, NudeMicroRNAsPancreatic NeoplasmsPrognosisProteasome Endopeptidase ComplexB7-H1 AntigenBiomarkers, TumorCD274 protein, humanLMP7 proteinMicroRNAsMIRN382 microRNA, humanProteasome Endopeptidase ComplexRNA, AntisenseRNA, Long NoncodingSTAT1 protein, humanSTAT1 Transcription FactormiR-382–3pPancreatic cancerPDL1PMSB8-AS1STAT1

Identifiers

PMID32891166
PMCPMC7487636
OpenAlexW3083239460

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.