Evidence map›Paper›PMID 30364632›Full record

ArticlePeerJ2018

Coordinative control of G2/M phase of the cell cycle by non-coding RNAs in hepatocellular carcinoma.

Jun Shi, Guangqiang Ye, Guoliang Zhao, Xuedong Wang, Chunhui Ye, Keooudone Thammavong, Jing Xu, Jiahong Dong

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  3. NClinical and translational medicine · 2022
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  8. Frontiers in cell and developmental biology · 2021
    Article
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  13. Mechano-signalling, induced by fullerene CInternational journal of nanomedicine · 2019
    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

8 authors at 3 institutions in 1 country.

Jun Shi *Department of Hepatobiliary and Pancreas Surgery, Beijing Tsinghua Changguang Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China.
Guangqiang Ye *The First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University, Nanning, China.
Guoliang ZhaoThe First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University, Nanning, China.
Xuedong WangDepartment of Hepatobiliary and Pancreas Surgery, Beijing Tsinghua Changguang Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China.
Chunhui YeThe First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University, Nanning, China.
Keooudone ThammavongThe First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University, Nanning, China.
Jing XuThe First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University, Nanning, China.
Jiahong DongDepartment of Hepatobiliary and Pancreas Surgery, Beijing Tsinghua Changguang Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China.
Beijing Tsinghua Chang Gung Hospital · CNGuangxi Medical University · CNFirst Affiliated Hospital of GuangXi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the interaction of non-coding RNAs (ncRNAs) in hepatocellular carcinoma.

methodsWe compared the ncRNAs and mRNAs expression profiles of hepatocellular carcinoma and adjacent tissue by microarray and RT-PCR. The relationship between different ncRNAs and mRNA was analyzed using bioinformatics tools. A regulatory model of ncRNAs in hepatocellular carcinoma cells was developed.

resultsA total of 1,704 differentially expressed lncRNAs, 57 miRNAs, and 2,093 mRNAs were identified by microarray analyses. There is a co-expression relationship between two ncRNAs (miRNA-125b-2-3p and lncRNA P26302). Bioinformatics analysis demonstrated cyclin-dependent kinases 1 and CyclinA2 as potential targets of miR-125b-2-3p and Polo-like kinase 1 as potential target of lncRNAP26302. All three gene are important components in the G2/M phase of cell cycle. Subsequently real-time polymerase chain reaction (PCR) studies confirmed these microarray results.

conclusionMiR-125b-2-3p and lncRNAP26302 may affect the G2/M phase of the cell cycle through the regulation of their respective target genes. This study shows a role of ncRNAs in pathogenesis of hepatocellular carcinoma at molecular level, providing a basis for the future investigation aiming at early diagnosis and novel treatment of hepatocellular carcinoma.

Indexed as

Hepatocellular carcinoma cellslncRNAMicroarraymiRNAmRNA

Identifiers

PMID30364632
PMCPMC6197396
OpenAlexW2896413769

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.