Evidence map›Paper›PMID 27543107›Full record

ArticleBMC cancer2016

Increased long noncoding RNA SNHG20 predicts poor prognosis in colorectal cancer.

Cong Li, Li Zhou, Jun He, Xue-Qing Fang, Shao-Wen Zhu, Mao-Ming Xiong

Abstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

46 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  19. Long Non-coding RNA Signature for Liver Metastasis of Colorectal Cancers.Frontiers in cell and developmental biology · 2021
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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.

Cong LiDepartment of Minimally Invasive Surgery, The People's Hospital of Chizhou, Chizhou, 247000, China.
Li ZhouDepartment of Minimally Invasive Surgery, The People's Hospital of Chizhou, Chizhou, 247000, China.
Jun HeDepartment of Minimally Invasive Surgery, The People's Hospital of Chizhou, Chizhou, 247000, China.
Xue-Qing FangDepartment of Minimally Invasive Surgery, The People's Hospital of Chizhou, Chizhou, 247000, China.
Shao-Wen ZhuDepartment of Minimally Invasive Surgery, The People's Hospital of Chizhou, Chizhou, 247000, China.
Mao-Ming XiongDepartment of General Surgery, First Hospital Affiliated to Anhui Medical University, Hefei, 230022, China. xiongmmahmu@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong noncoding RNAs (lncRNAs) have been suggested to be involved in the development and progression of malignancies. However, the investigation of small nucleolar RNA host gene 20 (SNHG20) on cancer progression remains unknown. The present study aims to explore the clinical significance of SNHG20 and its potential molecular mechanism in colorectal cancer (CRC).

methodsQuantitative real-time PCR (qRT-PCR) was used to measure the SNHG20 expression in a total of 107 CRC tissues and CRC cell lines. Loss of function approach was employed to explore the biological roles of SNHG20 in vitro. Its potential molecular mechanism was further verified by western blotting and qRT-PCR.

resultsThe results suggested that SNHG20 expression was significantly upregulated in CRC tissues compared to corresponding normal tissues from 107 CRC patients. High expression of SNHG20 was remarkably associated with advanced TNM stage in patients with CRC. Multivariate analyses unraveled that SNHG20 expression was an independent prognostic factor for overall survival in CRC patients. Further functional assays revealed that knockdown of SNHG20 suppressed cell proliferation, invasion and migration, and cell cycle progression in CRC cells. Moreover, SNHG20 regulated cell growth through modulation of a series of cell cycle-associated genes.

conclusionsOur findings suggest that dysregulation of SNHG20 participates in CRC progression and may serve as a potential therapeutic target in CRC patients.

Indexed as

Up-RegulationApoptosisCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease ProgressionFemaleGene Expression Regulation, NeoplasticHCT116 CellsHT29 CellsHumansMalePrognosisRNA, Long NoncodingSurvival Analysislong non-coding RNA SNHG20, humanRNA, Long NoncodingCell cycleColorectal cancerLong noncoding RNASNHG20

Identifiers

PMID27543107
PMCPMC4992210

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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.