Evidence map›Paper›PMID 34863279›Full record

ArticleBiology direct2021

Study on the mechanism of LOXL1-AS1/miR-3614-5p/YY1 signal axis in the malignant phenotype regulation of hepatocellular carcinoma.

ZhenYu Feng, ZhenYu Ye, JiaMing Xie, Wei Chen, Wei Li, ChunGen Xing

Open access · goldAbstract read
In one paragraph

Article in Biology direct, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  6. Article
  7. Review
  8. Making Sense of Antisense lncRNAs in Hepatocellular Carcinoma.International journal of molecular sciences · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. IFN-I inducibleFrontiers in immunology · 2022
    Article
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 2 institutions in 1 country.

ZhenYu FengDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, China.
ZhenYu YeDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, China.
JiaMing XieDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, China.
Wei ChenDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, China.
Wei LiDepartment of Hepatobiliary Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, China.
ChunGen XingDepartment of General Surgery, The Second Affiliated Hospital of Soochow University, No. 1055 Sanxiang Road, Gusu District, Suzhou, 215004, Jiangsu, China. xingchungen@sohu.com.
Second Affiliated Hospital of Soochow University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the most common malignant tumors with high mortality worldwide. Accumulating researches have indicated that long non‑coding RNAs (lncRNAs) are involved in varies human cancers, including HCC. Nevertheless, the specific molecular mechanism of lncRNA lysyl oxidase like 1 antisense RNA 1 (LOXL1-AS1) in HCC is still unclear.

methodsLOXL1-AS1 expression was tested via qRT-PCR in HCC cells. Functional and mechanism assays were respectively done to evaluate the biological functions of HCC cells and the potential interaction of LOXL1-AS1 and other factors.

resultsWe discovered that LOXL1-AS1 was high expressed in HCC cells. Inhibition of LOXL1-AS1 repressed cell proliferation, migration and invasion, but enhanced cell apoptosis in HCC. Further, miR-3614-5p was proven to be sponged by LOXL1-AS1. Additionally, Yin Yang 1 (YY1) was proven as the target gene of miR-3614-5p, and YY1 depletion could repress HCC cell malignant behaviors. YY1 could also transcriptionally activate LOXL1-AS1 expression. In rescue assays, we confirmed that overexpression of YY1 or miR-3614-5p inhibition could reverse the suppressive effects of LOXL1-AS1 silence on the malignant behaviors of HCC cells.

conclusionIn short, LOXL1-AS1/miR-3614-5p/YY1 forms a positive loop in modulating HCC cell malignant behaviors.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsRNA, Long NoncodingAmino Acid OxidoreductasesCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansPhenotypeYY1 Transcription FactorAmino Acid OxidoreductasesLOXL1 protein, humanMicroRNAsRNA, Long NoncodingYY1 protein, humanYY1 Transcription FactorHepatocellular carcinomaLOXL1-AS1miR-3614-5pYY1

Identifiers

PMID34863279
PMCPMC8645132
OpenAlexW4200022574

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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.