Evidence map›Paper›PMID 26823713›Full record

ArticleInternational journal of clinical and experimental pathology2015

MiR-211 inhibits cell proliferation and invasion of gastric cancer by down-regulating SOX4.

Chen-Yu Wang, Long Hua, Juan Sun, Kun-Hou Yao, Jiang-Tao Chen, Jun-Jie Zhang, Jun-Hong Hu

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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

25 citing papers in PubMed.

  1. Circular RNA circMTO1 suppressed the progression of renal cell carcinoma progression by sponging miR-211 and miR-204.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
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  11. MiRNA-134 suppresses esophageal squamous cell carcinoma progression by targeting FOXM1.International journal of clinical and experimental pathology · 2019
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  20. Propofol Suppresses Esophageal Squamous Cell Carcinoma Cell Migration and Invasion by Down-Regulation of Sex-Determining Region Y-box 4 (SOX4).Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
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

7 authors.

Chen-Yu WangDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.
Long HuaDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.
Juan SunSchool of Nursing, Xinxiang Medical University Xinxiang 453000, Henan Province, China.
Kun-Hou YaoDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.
Jiang-Tao ChenDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.
Jun-Jie ZhangDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.
Jun-Hong HuDepartment of General Surgery, Huaihe Hospital of Henan University Kaifeng 475000, Henan Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrevious studies have shown that the dysregulation of miRNAs are frequently associated with cancer progression. Deregulation of miR-211 has been observed in various types of human cancers. However, its biological function in gastric cancer (GC) is still unknown.

methodsThe expression of miR-211 in GC was detected by using quantitative real-time PCR (qRT-PCR). The miR-211 mimics and inhibitor were designed and transfected into BGC-823 cells. Then, we explore the probable biological function of miR-211 in gastric cancer cell proliferation and invasion in vitro. A luciferase reporter assay and western blot were performed to confirm the target gene of miR-211.

resultsMiR-211 was significantly down-regulated in GC. Over-expression of miR-211 inhibited gastric cancer cell proliferation and invasion in vitro, conversely, down-regulated expression of miR-211 promoted gastric cancer cell proliferation and invasion. In addition, the sex-determining region Y-related high mobility group box 4 (SOX4) is identified as a target of miR-211 in GC cells, and SOX4 expression levels was inversely correlated with miR-211. Furthermore, knockdown of Sox4 inhibited the proliferation and invasion in GC cells.

conclusionmiR-211 could inhibit GC cell proliferation and invasion partially by down-regulating SOX4. MiR-211 might be a potential therapeutic target for GC treatment in the future.

Indexed as

Cell MovementCell ProliferationCell Line, TumorDown-RegulationGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm InvasivenessSignal TransductionSOXC Transcription FactorsStomach NeoplasmsTime FactorsTransfectionMicroRNAsMIRN211 microRNA, humanSOX4 protein, humanSOXC Transcription FactorsGastric cancerinvasionmiR-211proliferationSOX4

Identifiers

PMID26823713
PMCPMC4713499

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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.