Evidence map›Paper›PMID 32725768›Full record

ArticleCancer medicine2020

Long noncoding RNA HCG18 up-regulates the expression of WIPF1 and YAP/TAZ by inhibiting miR-141-3p in gastric cancer.

Yan Liu, Wenji Lin, Yangyang Dong, Xinyu Li, Zhibin Lin, Jing Jia, Wenbing Zou, Yu Pan

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

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  9. The regulatory role of LncRNA HCG18 in various cancers.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
  10. The Hippo signaling pathway in gastric cancer.Acta biochimica et biophysica Sinica · 2023
    Review
  11. The role of long non-coding RNA HCG18 in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
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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

8 authors at 1 institution in 1 country.

Yan LiuDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.ORCID 0000-0002-8826-5948
Wenji LinDepartment of Radiology, Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Yangyang DongDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Xinyu LiDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Zhibin LinDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Jing JiaDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Wenbing ZouDepartment of Gastrointestinal Surgery (#2), Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, China.
Yu PanDepartment of General Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Fujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccumulating works show that lncRNAs play critical roles in the development of gastric cancer (GC). LncRNA HLA complex group 18 (HCG18) was implicated in the progression of bladder cancer and glioma, but its role in GC is unknown.

methodsRT-PCR was used to detect HCG18 and miR-141-3p expression in GC specimen. GC cell lines (AGS and MKN-28) were exploited as cell model. The biological effect of HCG18 on cancer cells was probed by CCK-8, colony formation, flow cytometry, Transwell and wound-healing experiments in vitro, and subcutaneous xenotransplanted tumor model and tail vein injection model in vivo. Interaction between HCG18 and miR-141-3p was determined by bioinformatics analysis, RT-PCR, and luciferase reporter experiments. Downstream gene expression of miR-141-3p, including Wiskott-Aldrich syndrome protein interacting protein family member 1 (WIPF1), Yes associated protein 1 (YAP), and tafazzin (TAZ) were detected using Western blot.

resultsHCG18 was markedly up-regulated in GC specimens, while miR-141-3p was markedly down-regulated. Down-regulation of HCG18 inhibited viability, migration, and invasion of GC cells, while miR-141-3p transfection led to opposite effect. HCG18 could down-regulate miR-141-3p through adsorbing it, and a negative association between HCG18 and miR-141-3p was found in GC specimens. HCG18 promoted WIPF1, YAP and TAZ expression, nonetheless, such influence was reversed by co-transfecting with miR-141-3p.

conclusionHCG18 was aberrantly up-regulated in GC tissues, and it indirectly regulated the activity of Hippo signaling through counteracting miR-141-3p expression.

Indexed as

AcyltransferasesAdaptor Proteins, Signal TransducingAdultAgedAnimalsCell Line, TumorCytoskeletal ProteinsFemaleGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMaleMice, Inbred BALB CMice, NudeMicroRNAsMiddle AgedAcyltransferasesAdaptor Proteins, Signal TransducingCytoskeletal ProteinsIntracellular Signaling Peptides and ProteinsMicroRNAsMIRN141 microRNA, humanRNA, Long NoncodingTAFAZZIN protein, humanTranscription FactorsWIPF1 protein, humanYAP1 protein, humanYAP-Signaling ProteinsHCG18invasionmigrationmiR-141-3pviability

Identifiers

PMID32725768
PMCPMC7520348
OpenAlexW3046212589

What OpenQuestion holds

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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.