Evidence map›Paper›PMID 28269753›Full record

ArticleCancer biomarkers : section A of Disease markers2017

LncRNA, NEAT1 is a prognosis biomarker and regulates cancer progression via epithelial-mesenchymal transition in clear cell renal cell carcinoma.

Li Ning, Zhiguo Li, Dianjun Wei, Haiyan Chen, Chao Yang

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

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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

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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

47 citing papers in PubMed, 76 citations in OpenAlex.

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  19. The Long Noncoding RNAMolecular cancer research : MCR · 2020
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Li NingDepartment of Clinical Laboratory, The Second Hospital of Tianjin Medical University, Tianjin, China.
Zhiguo LiDepartment of Clinical Laboratory, The Second Hospital of Tianjin Medical University, Tianjin, China.
Dianjun WeiDepartment of Clinical Laboratory, The Second Hospital of Tianjin Medical University, Tianjin, China.
Haiyan ChenDepartment of Nephrology, The Second Hospital of Tianjin Medical University, Tianjin, China.
Chao YangDepartment of Clinical Laboratory, The First Affiliated Hospital of Xi'an Medical University, Xi'an, Shaanxi, China.
Second Hospital of Tianjin Medical University · CNTianjin Medical University · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe long non-coding RNAs (lncRNAs) are emerging as important regulators in cancer progression. Clear cell renal cell carcinoma (ccRCC) is one of the most common urological cancers with poor prognosis. In this study, we examined the functional role of the lncRNA, nuclear enriched abundant transcript 1 (NEAT1) in ccRCC progression.

methodsWe performed quantitative real time PCR and western blotting assays to measure mRNA and protein expression levels, respectively. CCK-8 assay, cell invasion and migration assays were used to determine the cell proliferative, cell invasive and migratory ability. Flow cytometric analysis was performed to examine cell apoptosis.

resultsThe expression levels of NEAT1 was up-regulated in ccRCC tissues and up-regulation of NETA1 was positively correlated with tumor size, higher Fuhrman grade, and lymph node metastasis, and also predicts worse 5-year survival rate of patients with ccRCC. NEAT1 knock-down by NEAT siRNAs transfection suppressed cell proliferation and induced cell apoptosis in ccRCC cell lines. In addition, NEAT1 knock-down suppressed cell invasion and migration and inhibited the mRNA and protein expression levels of epithelial-mesenchymal transition-related markers in ccRCC cell lines.

conclusionsIn conclusion, NEAT1 may be an important mediator in the regulation of ccRCC progression and predicts the poor prognosis in patients with ccRCC.

Indexed as

ApoptosisBiomarkers, TumorCarcinoma, Renal CellCell Line, TumorCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMaleNeoplasm InvasivenessPrognosisRNA, Long NoncodingBiomarkers, TumorNEAT1 long non-coding RNA, humanRNA, Long NoncodingccRCCepithelial-mesenchymal transitionlncRNANEAT1prognosisprogression

Identifiers

PMID28269753
PMCPMC13020697
OpenAlexW2594577398

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.