Evidence map›Paper›PMID 25025236›Full record

ArticlePloS one2014

The long noncoding RNA expression profile of hepatocellular carcinoma identified by microarray analysis.

Juanjuan Zhu, Shanshan Liu, Fuqiang Ye, Yuan Shen, Yi Tie, Jie Zhu, Yinghua Jin, Xiaofei Zheng, Yongge Wu, Hanjiang Fu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.1field-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

37 citing papers in PubMed, 59 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

10 authors at 2 institutions in 1 country.

Juanjuan ZhuCollege of Life Sciences, Jilin University, Changchun, China; Beijing Institute of Radiation Medicine, Beijing, China.
Shanshan LiuCollege of Life Sciences, Jilin University, Changchun, China; Beijing Institute of Radiation Medicine, Beijing, China.
Fuqiang YeBeijing Institute of Radiation Medicine, Beijing, China.
Yuan ShenBeijing Institute of Radiation Medicine, Beijing, China.
Yi TieBeijing Institute of Radiation Medicine, Beijing, China.
Jie ZhuBeijing Institute of Radiation Medicine, Beijing, China.
Yinghua JinCollege of Life Sciences, Jilin University, Changchun, China.
Xiaofei ZhengBeijing Institute of Radiation Medicine, Beijing, China.
Yongge WuCollege of Life Sciences, Jilin University, Changchun, China.
Hanjiang FuBeijing Institute of Radiation Medicine, Beijing, China.
Beijing Radiation Center · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThousands of long noncoding RNAs (lncRNAs) have been reported in mammalian genomes. These RNAs represent an important subset of pervasive genes involved in a broad range of biological functions. Aberrant expression of lncRNAs is associated with many types of cancers. Here, in order to explore the potential lncRNAs involved in hepatocellular carcinoma (HCC) oncogenesis, we performed lncRNA gene expression profile analysis in 3 pairs of human HCC and adjacent non-tumor (NT) tissues by microarray. METHODOLOGY: Differentially expressed lncRNAs and mRNAs were detected by human lncRNA microarray containing 33,045 lncRNAs and 30,215 coding transcripts. Bioinformatic analyses (gene ontology, pathway and network analysis) were applied for further study of these differentially expressed mRNAs. By qRT-PCR analysis in nineteen pairs of HCC and adjacent normal tissues, we found that eight lncRNAs were aberrantly expressed in HCC compared with adjacent NT tissues, which is consistent with microarray data.

conclusionsWe identified 214 lncRNAs and 338 mRNAs abnormally expressed in all three HCC tissues (Fold Change ≥2.0, P<0.05 and FDR <0.05) with the genome-wide lncRNAs and mRNAs expression profile analysis. The lncRNA-mRNA co-expression network was constructed, which may be used for predicting target genes of lncRNAs. Furthermore, we demonstrated for the first time that BC017743, ENST00000395084, NR_026591, NR_015378 and NR_024284 were up-regulated, whereas NR_027151, AK056988 and uc003yqb.1 were down-regulated in nineteen pairs of HCC samples compared with adjacent NT samples. Expression of seven lncRNAs was significantly correlated to their nearby coding genes. In conclusion, our results indicated that the lncRNA expression profile in HCC was significantly changed, and we identified a series of new hepatocarcinoma associated lncRNAs. These results provide important insights about the lncRNAs in HCC pathogenesis.

Indexed as

RNA, Long NoncodingTranscriptomeAdultCarcinoma, HepatocellularComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyGene Regulatory NetworksHumansLiver NeoplasmsMaleMiddle AgedReproducibility of ResultsRisk FactorsRNA, MessengerRNA, Long NoncodingRNA, Messenger

Identifiers

PMID25025236
PMCPMC4099127
OpenAlexW2055509265

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.