Evidence map›Paper›PMID 33243205›Full record

SynthesisBMC cancer2020

Long non-coding RNA SNHG15 in various cancers: a meta and bioinformatic analysis.

Caizhi Chen, Yeqian Feng, Jingjing Wang, Ye Liang, Wen Zou

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
0.6field-weighted citation impact, top 38% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 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

5 authors at 1 institution in 1 country.

Caizhi ChenDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
Yeqian FengDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
Jingjing WangDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
Ye LiangDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
Wen ZouDepartment of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China. zouwen29w@csu.edu.cn.ORCID http://orcid.org/0000-0001-6398-0649
Central South University · CN

Funding

Development and Reform Commission of Hunan Province (2019)412
6 · The paper itself

Abstract

backgroundThe snoRNA host gene SNHG15 produces a long non-coding RNA (lncRNA) with a short half-life and has been reported to be dysregulated in multiple cancers and has recently been found to be correlated with tumour progression. Therefore, this meta-analysis was performed to evaluate the generalised prognostic role of small nucleolar RNA host gene 15 (SNHG15) in malignancies, based on variable data from different studies.

methodsFour public databases were used to identify eligible studies. The association between prognostic indicators and clinical features was extracted and pooled to estimate the hazard ratios (HRs) or odds ratios (ORs) with 95% confidence intervals (CIs). Publication bias was measured using Begg's test and Egger's test, and the stability of pooled results were measured using sensitivity analysis. Additionally, an online database based on The Cancer Genome Atlas (TCGA) was screened to further validate our results. Ultimately, we predicted the molecular regulation of SNHG15 based on the public databases.

resultsIn total, 11 studies including 1087 patients were ultimately enrolled in our meta-analysis. We found that SNHG15 overexpression was associated with worse overall survival (OS) and disease-free survival (DFS), and this was validated in the Gene Expression Profiling Interactive Analysis (GEPIA) cohort. Moreover, increased SNHG15 expression suggested advanced TNM stage and LNM, but was not associated with age, gender, or tumour size. No publication bias or instability of the results was observed. SNHG15 was significantly upregulated in seven cancers and elevated expression of SNHG15 indicated shorter OS and DFS in five malignancies based on the validation using the GEPIA cohort. Further functional prediction indicated that SNHG15 may participate in some cancer-related pathways.

conclusionsUpregulation of lncRNA SNHG15 was notably associated with worse prognosis and clinical features, suggesting that SNHG15 might serve as a novel prognostic factor in various cancers.

Indexed as

Computational BiologyFemaleHumansMaleMiddle AgedNeoplasmsPrognosisRNA, Long NoncodingRNA, Long NoncodingBioinformaticsLncRNA SNHG15Meta-analysisPrognosis

Identifiers

PMID33243205
PMCPMC7690101
OpenAlexW3107583319

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.