Evidence map›Paper›PMID 29949944›Full record

ArticleGenes2018

Investigating the Promoter of FAT10 Gene in HCC Patients.

Shuaichen Liu, Yu Jin, Dongwei Zhang, Jingbo Wang, Guangyi Wang, Caroline G L Lee

Open access · goldAbstract read
In one paragraph

Article in Genes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Shuaichen LiuDepartment of Hepatobiliary & Pancreas Surgery, The First Hospital, Jilin University, Changchun 130021, China. liuscmd@163.com.
Yu JinDivision of Medical Sciences, National Cancer Center, Singapore 169610, Singapore. jin.yu@nccs.com.sg.
Dongwei ZhangDepartment of Biochemistry, National University of Singapore, Singapore 119077, Singapore. dongwei_z@hotmail.com.
Jingbo WangDepartment of Biochemistry, National University of Singapore, Singapore 119077, Singapore. jingbowang1980@hotmail.com.
Guangyi WangDepartment of Hepatobiliary & Pancreas Surgery, The First Hospital, Jilin University, Changchun 130021, China. wgymd@sina.com.
Caroline G L LeeDepartment of Biochemistry, National University of Singapore, Singapore 119077, Singapore. bchleec@nus.edu.sg.ORCID 0000-0002-4323-3635
National University of Singapore · SGJilin University · CNNational Cancer Centre Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FAT10, which is also known as diubiquitin, has been implicated to play important roles in immune regulation and tumorigenesis. Its expression is up-regulated in the tumors of Hepatocellular Carcinoma (HCC) and other cancer patients. High levels of FAT10 in cells have been shown to result in increased mitotic non-disjunction and chromosome instability, leading to tumorigenesis. To evaluate whether the aberrant up-regulation of the FAT10 gene in the tumors of HCC patients is due to mutations or the aberrant methylation of CG dinucleotides at the FAT10 promoter, sequencing and methylation-specific sequencing of the promoter of FAT10 was performed. No mutations were found that could explain the differential expression of FAT10 between the tumor and non-tumorous tissues of HCC patients. However, six single nucleotide polymorphisms (SNPs), including one that has not been previously reported, were identified at the promoter of the FAT10 gene. Different haplotypes of these SNPs were found to significantly mediate different FAT10 promoter activities. Consistent with the experimental observation, differential FAT10 expression in the tumors of HCC patients carrying haplotype 1 was generally higher than those carrying haplotype II. Notably, the methylation status of this promoter was found to correlate with FAT10 expression levels. Hence, the aberrant overexpression of the FAT10 gene in the tumors of HCC patients is likely due to aberrant methylation, rather than mutations at the FAT10 promoter.

Indexed as

expressionFAT10methylationpromoterSNPs

Identifiers

PMID29949944
PMCPMC6070910
OpenAlexW2810407048

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.