Evidence map›Paper›PMID 30185552›Full record

ArticleCancer research2018

EGR1-Mediated Transcription of lncRNA-HNF1A-AS1 Promotes Cell-Cycle Progression in Gastric Cancer.

Hai-Ting Liu, Sen Liu, Lei Liu, Ran-Ran Ma, Peng Gao

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 1% 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

117 citing papers in PubMed, 1 synthesis or guideline pooled it, 191 citations in OpenAlex.

  1. Pooled it
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  16. METTL3-mediated mCellular & molecular biology letters · 2024
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57 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Hai-Ting LiuDepartment of Pathology, School of Medicine, Shandong University, Jinan, P. R. China.
Sen LiuDepartment of Pathology, School of Medicine, Shandong University, Jinan, P. R. China.
Lei LiuDepartment of Pathology, School of Medicine, Shandong University, Jinan, P. R. China.
Ran-Ran MaDepartment of Pathology, School of Medicine, Shandong University, Jinan, P. R. China.
Peng GaoDepartment of Pathology, School of Medicine, Shandong University, Jinan, P. R. China. gaopeng@sdu.edu.cn.
Shandong University · CN

Funding

NIH Health DisparitiesR01ES017407 · NIEHS · MASSACHUSETTS STATE DEPT OF PUB HEALTH · PI SANDEL, MEGAN T, SMITH, LAUREN A. · 2009 to 2010
$928k
NIEHS NIH HHS R01 ES017407
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNA) are dysregulated in various human cancers and control tumor development and progression. However, the upstream mechanisms underlying their dysregulation remain unclear. Here, we demonstrate that the expression of hepatocyte nuclear factor 1 homeobox A antisense RNA 1 (HNF1A-AS1) is significantly upregulated in gastric cancer tissues. Overexpression of HNF1A-AS1 enhanced cell proliferation and promoted cell-cycle progression, whereas knockdown of HNF1A-AS1 elicited the opposite effects. Early growth response protein 1 (EGR1) directly bound the HNF1A-AS1 promoter region and activated its transcription. Overexpression of EGR1 enhanced cell proliferation and promoted cell-cycle promotion, similar to the function of HNF1A-AS1. HNF1A-AS1 functioned as competing endogenous RNA (ceRNA) by binding to miR-661, upregulating the expression of cell division cycle 34 (CDC34), which is a direct target of miR-661. EGR1 and HNF1A-AS1 enhanced the expression of cyclin-dependent kinase 2 (CDK2), CDK4, and cyclin E1 but inhibited the expression of p21 by promoting CDC34-mediated ubiquitination and degradation of p21. Taken together, these findings suggest that EGR1-activated HNF1A-AS1 regulates various pro- and antigrowth factors to promote the development of gastric cancer, implicating it as a possible target for therapeutic intervention in this disease.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisCell CycleCell Line, TumorCell MovementCell ProliferationCyclin-Dependent Kinase 4Cyclin ECycloheximideDactinomycinDisease ProgressionEarly Growth Response Protein 1HumansMaleMiceCCNE1 protein, humanCDC34 protein, humanCDK4 protein, humanCyclin-Dependent Kinase 4Cyclin ECycloheximideDactinomycinEarly Growth Response Protein 1EGR1 protein, humanlong non-coding RNA HNF1A-AS1, humanMicroRNAsOncogene ProteinsRNA, AntisenseRNA, Long NoncodingRNA, Small InterferingUbiquitin-Conjugating Enzymes

Identifiers

PMID30185552
PMCPMC6191331
OpenAlexW2891412523

What OpenQuestion holds

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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.