Evidence map›Paper›PMID 32930970›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2021

Long non-coding RNA SNHG3, induced by IL-6/STAT3 transactivation, promotes stem cell-like properties of gastric cancer cells by regulating the miR-3619-5p/ARL2 axis.

Bo Sun, Yang Han, Hong Cai, Hua Huang, Yi Xuan

RetractedAbstract readRetracted Publication
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Signaling pathways and therapeutic interventions in gastric cancer.Signal transduction and targeted therapy · 2022
    Review
  3. Article
  4. Review
  5. Article
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  17. [Role of long noncoding RNA SNHG3 in regulating proliferation, migration and invasion of cervical cancer SiHa cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Bo Sun *Department of Gastric Surgery, Fudan University Shanghai Cancer Center, No. 270 Dongan Road, 200032, Shanghai, China.
Yang Han *Department of Gastric Surgery, Fudan University Shanghai Cancer Center, No. 270 Dongan Road, 200032, Shanghai, China.
Hong CaiDepartment of Gastric Surgery, Fudan University Shanghai Cancer Center, No. 270 Dongan Road, 200032, Shanghai, China. caihong450@hotmail.com.
Hua HuangDepartment of Gastric Surgery, Fudan University Shanghai Cancer Center, No. 270 Dongan Road, 200032, Shanghai, China. huahuang@fudan.edu.cn.
Yi XuanDepartment of Gastric Surgery, Fudan University Shanghai Cancer Center, No. 270 Dongan Road, 200032, Shanghai, China. xuanyi0118@126.com.
Fudan University Shanghai Cancer Center · CN

Funding

Shanghai Anticancer Association "aoxiang" Project SACA-AX201901
6 · The paper itself

Abstract

backgroundChemotherapy is, next to surgery and radiotherapy, the mainstay regimen for the clinical management of gastric cancer. This therapy is, however, heavily compromised by the acquisition of resistance. Here, we aimed to clarify the potential involvement of long non-coding RNA SNGH3 in the acquisition of cisplatin resistance and stemness in gastric cancer.

methodsCell viability and proliferation were measured using Cell Counting Kit-8 and colony formation assays, respectively. Stem cell-like cell growth was evaluated using a mammosphere formation assay. RNA levels of SNHG2, OCT-4, SOX-2, CD44, miR-3619-5p and ARL2 were determined using qRT-PCR, whereas protein levels of OCT-4, SOX-2, CD44, ARL2, STAT3 and pSTAT3 were determined using Western blotting. Dual luciferase reporter assays were employed to interrogate regulatory interactions between STAT3, SNHG3, miR-3619-5p and ARL2, respectively. Direct binding of STAT3 to the SNHG3 promoter was investigated using a chromatin immunoprecipitation assay.

resultsWe found that IL-6 triggered stem cell-like properties in cisplatin-treated gastric cancer cells and activated STAT3, which in turn transcriptionally regulated SNHG3 expression. SNHG3 expression up-regulation positively correlated with cisplatin resistance and stemness of gastric cancer cells, while SNHG3 down-regulation inhibited stem cell-like properties. In addition, we found that SNHG3 up-regulated ARL2 expression through sponging miR-3619-5p, which predominantly mediated the oncogenic properties of SNHG3 in this disease.

conclusionsOur data indicate an involvement of aberrant SNHG3 over-expression in the acquisition of both cisplatin resistance and stemness of gastric cancer cells, and of the IL-6/STAT3/SNHG3/miR-3619-5p/ARL2 signaling cascade in the oncogenic properties of SNHG3.

Indexed as

Base SequenceCell Line, TumorCisplatinDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticGene Knockdown TechniquesGTP-Binding ProteinsHumansInterleukin-6MicroRNAsModels, BiologicalNeoplastic Stem CellsRNA, Long NoncodingSTAT3 Transcription FactorStomach NeoplasmsTranscriptional ActivationARL2 protein, humanCisplatinGTP-Binding ProteinsInterleukin-6MicroRNAsMIRN-3619 microRNA, humanRNA, Long NoncodingSTAT3 Transcription Factorcisplatin resistancegastric cancermiR-3619-5pSNHG3stem cell

Identifiers

PMID32930970
PMCPMC12980753
OpenAlexW3085708708

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.