Evidence map›Paper›PMID 32920660›Full record

ArticleDigestive diseases and sciences2021

SNHG10 Promotes Cell Proliferation and Migration in Gastric Cancer by Targeting miR-495-3p/CTNNB1 Axis.

Xiu Yuan, Tianwen Yang, Yun Xu, Shan Ou, Peng Shi, Ming Cao, Xin Zuo, Qinglan Liu, Jie Yao

Abstract read
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In one paragraph

Article in Digestive diseases and sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. The Functions and Mechanisms of Long Non-coding RNA SNHGs in Gastric Cancer.Combinatorial chemistry & high throughput screening · 2024
    Review
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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

9 authors at 1 institution in 1 country.

Xiu YuanDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Tianwen YangDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Yun XuDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Shan OuDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Peng ShiDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Ming CaoDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Xin ZuoDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Qinglan LiuDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China.
Jie YaoDepartment of Gastroenterology, The Sixth People's Hospital of Chongqing, Chongqing, 400000, China. jrek06@163.com.ORCID 0000-0003-2568-6777
First People's Hospital of Chongqing · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong non-coding RNAs have been acknowledged as the crucial regulators in the progression of human cancers, including gastric cancer (GC). Small nucleolar RNA host gene 10 (SNHG10) has been identified as an oncogene in several cancer types. Nonetheless, it is unclear whether SNHG10 exerts functions in GC cells.

aimsThe aims of the current study were to explore the function and underlying mechanism of SNHG10 in GC.

methodsThe expression levels of SNHG10, miR-495-3p and catenin beta 1 (CTNNB1) were detected by RT-qPCR. Loss-of-function assays, including CCK-8, colony formation assay, flow cytometry analysis and transwell assays, were conducted to verify the effect of SHNG10 on the proliferation, apoptosis, migration and invasion of GC cells. Mechanism experiments were performed to identify the downstream molecular mechanism of SNHG10.

resultsSNHG10 was expressed at a high level in GC cells. Knockdown of SNHG10 inhibited the proliferation, migration and invasion of GC cells. Silencing of SNHG10 led to the downregulation of core factors of WNT signaling pathway. Knockdown of SNHG10 could decline the expression of CTNNB1 through sequestering miR-495-3p.

conclusionsSNHG10 promotes the procession of GC through targeting miR-495-3p/CTNNB1 and activating WNT signaling pathway.

Indexed as

beta CateninCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGene SilencingHumansMicroRNAsRNA, Long NoncodingStomach Neoplasmsbeta CateninCTNNB1 protein, humanMicroRNAsMIRN495 microRNA, humanRNA, Long NoncodingCTNNB1Gastric cancermiR-495-3pSNHG10

Identifiers

PMID32920660
OpenAlexW3085022185

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.