Evidence map›Paper›PMID 34092977›Full record

ArticleWorld journal of gastroenterology2021

Upregulation of long noncoding RNA W42 promotes tumor development by binding with DBN1 in hepatocellular carcinoma.

Guang-Lin Lei, Yan Niu, Si-Jie Cheng, Yuan-Yuan Li, Zhi-Fang Bai, Ling-Xiang Yu, Zhi-Xian Hong, Hu Liu, Hong-Hong Liu, Jin Yan and 5 more

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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  10. New Insights into LINC00346 and its Role in Disease.Frontiers in cell and developmental biology · 2021
    Review
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

15 authors at 1 institution in 1 country.

Guang-Lin LeiFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Yan NiuInner Mongolia Medical University, Hohhot 010110, Inner Mongolia Autonomous Region, China.
Si-Jie ChengFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Yuan-Yuan LiFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Zhi-Fang BaiFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Ling-Xiang YuFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Zhi-Xian HongFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Hu LiuFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Hong-Hong LiuFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Jin YanFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Yuan GaoFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Shao-Geng ZhangFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Zhu ChenFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Rui-Sheng LiFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China.
Peng-Hui YangFifth Medical Center of Chinese PLA General Hospital, Beijing 100039, China. ypenghuiamms@hotmail.com.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a malignancy found globally. Accumulating studies have shown that long noncoding RNAs (lncRNAs) play critical roles in HCC. However, the function of lncRNA in HCC remains poorly understood.

aimTo understand the effect of lncRNA W42 on HCC and dissect the underlying molecular mechanisms.

methodsWe measured the expression of lncRNA W42 in HCC tissues and cells (Huh7 and SMMC-7721) by quantitative reverse transcriptase polymerase chain reaction. Receiver operating characteristic curves were used to assess the sensitivity and specificity of lncRNA W42 expression. HCC cells were transfected with pcDNA3.1-lncRNA W42 or shRNA-lncRNA W42. Cell functions were detected by cell counting Kit-8 (CCK-8), colony formation, flow cytometry and Transwell assays. The interaction of lncRNA W42 and DBN1 was confirmed by RNA immunoprecipitation and RNA pull down assays. An HCC xenograft model was used to assess the role of lncRNA W42 on tumor growth

resultsIn this study, we identified a novel lncRNA (lncRNA W42), and investigated its biological functions and clinical significance in HCC. LncRNA W42 expression was upregulated in HCC tissues and cells. Overexpression of lncRNA W42 notably promoted the proliferative and invasion of HCC, and inhibited cell apoptosis. LncRNA W42 directly bound to DBN1 and activated the downstream pathway. LncRNA W42 knockdown suppressed HCC xenograft tumor growth

conclusion

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsRNA, Long NoncodingCell ProliferationGene Expression Regulation, NeoplasticHumansUp-RegulationRNA, Long NoncodingCancerDBN1Hepatocellular carcinomaLong noncoding RNALong noncoding RNA W42Tumor

Identifiers

PMID34092977
PMCPMC8160624
OpenAlexW3164108904

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.