Evidence map›Paper›PMID 32184620›Full record

ArticleOncoTargets and therapy2020

MicroRNA Profile Identifies miR-6165 Could Suppress Gastric Cancer Migration and Invasion by Targeting STRN4.

Zhu Wang, Yang Li, Jian Cao, Wei Zhang, Quan Wang, Zhen Zhang, Zhidong Gao, Yingjiang Ye, Kewei Jiang, Shan Wang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 48% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Microrna Expression inMicroRNA (Shariqah, United Arab Emirates) · 2026
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  3. Review
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  6. CD8Frontiers in immunology · 2022
    Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Zhu WangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Yang LiDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Jian CaoDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Wei ZhangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.ORCID 0000-0002-2001-1052
Quan WangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Zhen ZhangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.ORCID 0000-0003-4657-0589
Zhidong GaoDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Yingjiang YeDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Kewei JiangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Shan WangDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing 100044, People's Republic of China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies showed that aberrant expression of miRNAs causes tumor-suppressing or promoting effects in various cancers including gastric cancer (GC). Our previous studies showed that lots of miRNAs and mRNA expressed differentially in GC and normal tissues. However, the critical miRNAs and mRNA need to be clarified. MATERIALS AND

methodsMicroarray sequencing was used to profile the differential expression of miRNAs and mRNA in GC and normal tissues. Bioinformatics analysis and database prediction were used to search the critical miRNAs and mRNA. Real-time quantitative polymerase chain reaction (RT-qPCR), luciferase reporter assay, immunohistochemistry (IHC), wound healing assay and transwell assay were used to clarify the relationship between the target miRNAs and mRNA. Statistical analysis was used to seek their value of diagnosis and prognosis.

resultsWe identified microRNA-6165 (miR-6165) as a novel cancer-related miRNA in GC through high-throughput microarray sequencing. By bioinformatics analysis and luciferase reporter assay, we found STRN4 was the target of miR-6165. Via a series of cell experiments, we determined that miR-6165 suppressed GC cells migration and invasion by targeting STRN4. Also, we discovered the potential diagnosis and prognosis value of miR-6165 and STRN4.

conclusionIt was found that miR-6165 might suppress GC migration and invasion by targeting STRN4 in vitro, and the further research should focus more on the potential diagnosis and prognosis value of miR-6165 and STRN4 in gastric cancer patients.

Indexed as

gastric cancermigration and invasionmiR-6165STRN4

Identifiers

PMID32184620
PMCPMC7060782
OpenAlexW3009253420

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.