Evidence map›Paper›PMID 35334500›Full record

ArticleJournal of clinical laboratory analysis2022

Biological and clinical implications of hsa_circ_0086720 in gastric cancer and its clinical application.

Yongfu Shao, Changlei Qi, Jianing Yan, Rongdan Lu, Guoliang Ye, Junming Guo

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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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 at 1 institution in 1 country.

Yongfu ShaoDepartment of Gastroenterology, The Affiliated Hospital of Medical School of Ningbo University, Ningbo, China.ORCID https://orcid.org/0000-0001-6256-1426
Changlei QiDepartment of Gastroenterology, The Affiliated Hospital of Medical School of Ningbo University, Ningbo, China.
Jianing YanDepartment of Biochemistry and Molecular Biology and Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.ORCID https://orcid.org/0000-0002-8781-9021
Rongdan LuDepartment of Gastroenterology, The Affiliated Hospital of Medical School of Ningbo University, Ningbo, China.
Guoliang YeDepartment of Gastroenterology, The Affiliated Hospital of Medical School of Ningbo University, Ningbo, China.ORCID https://orcid.org/0000-0003-0600-9981
Junming GuoDepartment of Biochemistry and Molecular Biology and Zhejiang Key Laboratory of Pathophysiology, Ningbo University School of Medicine, Ningbo, China.ORCID https://orcid.org/0000-0003-2026-1075
Ningbo University · CN

Funding

Key Scientific and Technological Projects of Ningbo 2021Z133National Natural Science Foundation of China 81702367Natural Science Foundation of Ningbo 202003N4198the Affiliated Hospital of Medical School of Ningbo University Youth Talent Cultivation Program FYQMKY202001the Youth Medical Backbone Talents Training Program of Ningbo
6 · The paper itself

Abstract

backgroundCircular RNAs (circRNAs) are thought to be vital participants in carcinogenesis and have the characteristics of being stable, specific, and well conserved. However, their clinical significance and application value in gastric cancer (GC) are still poorly understood. Hsa_circ_0086720 was found to be a dysregulated circRNA in GC by microarray screening and was further explored for its clinical significance and application.

methodsHsa_circ_0086720 was detected in GC cell lines, tissues, and plasma, and the clinicopathological correlations were investigated. The existence, stability, origin, and change in the plasma hsa_circ_0086720 level were verified in early GC patients. Moreover, receiver operating characteristic and Kaplan-Meier survival curves were constructed to analyze the diagnostic and prognostic values, and bioinformatics analysis was used to identify the potential functions. Finally, risk factors and nomogram predicting were established.

resultsHsa_circ_0086720 was found to be downregulated in gastric carcinogenesis, and tissue hsa_circ_0086720 was negatively associated with perineural invasion, Borrmann type, disease-free survival, and overall survival. Hsa_circ_0086720 was stable in circulating plasma and was actively secreted by cells in gastric carcinogenesis. As a biomarker for early GC screening, plasma hsa_circ_0086720 had good sensitivity and specificity, and its stability met the clinical application requirements. Bioinformatics analysis suggested that dysregulated hsa_circ_0086720 has important functions in gastric carcinogenesis. Univariate Cox regression analysis identified factors associated with overall survival time and disease-free survival time. The nomograms showed good accuracy of predicting survival time.

conclusionHsa_circ_0086720 is a novel biomarker for screening early GC and predicting the prognosis of advanced-stage patients.

Indexed as

Stomach NeoplasmsBiomarkers, TumorCarcinogenesisHumansPrognosisRNA, CircularBiomarkers, TumorRNA, CircularbiomarkerCircRNAgastric cancerhsa_circ_0086720prognosis

Identifiers

PMID35334500
PMCPMC9102612
OpenAlexW4220695792

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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.