Evidence map›Paper›PMID 29679339›Full record

ArticleHuman cell2018

Long non-coding RNA (lncRNA) MAGI2-AS3 inhibits breast cancer cell growth by targeting the Fas/FasL signalling pathway.

Yong Yang, Hong Yang, Miao Xu, Haibin Zhang, Mingtao Sun, Peng Mu, Tongbao Dong, Shanmei Du, Kui Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

53 citing papers in PubMed, 84 citations in OpenAlex.

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  12. MicroRNA Expression Profile in Early-Stage Breast Cancers.MicroRNA (Shariqah, United Arab Emirates) · 2024
    Article
  13. Metformin and long non-coding RNAs in breast cancer.Journal of translational medicine · 2023
    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 6 institutions in 1 country.

Yong YangAffiliated Hospital of Taishan Medical University, Tai'an, 271000, Shandong, People's Republic of China.
Hong YangCentral Hospital of Tai'an City, Tai'an, 271000, Shandong, People's Republic of China.
Miao XuThe Seventh People's Hospital of Zibo, Zibo, 255040, Shandong, People's Republic of China.
Haibin ZhangQingzhou People's Hospital, Qingzhou, 262500, Shandong, People's Republic of China.
Mingtao SunZibo Vocational Institute, Zibo, 255314, Shandong, People's Republic of China.
Peng MuZibo Vocational Institute, Zibo, 255314, Shandong, People's Republic of China.
Tongbao DongZibo Vocational Institute, Zibo, 255314, Shandong, People's Republic of China.
Shanmei DuZibo Vocational Institute, Zibo, 255314, Shandong, People's Republic of China. dushanmei@126.com.
Kui LiuCenter of Translational Medicine, Zibo Central Hospital, 54# Gongqingtuan Road, Zibo, 255036, Shandong, People's Republic of China. liukui37190158@163.com.
Zibo Vocational Institute · CNAffiliated Hospital of Taishan Medical University · CNCentral Hospital of Zibo · CNQingzhou City People's Hospital · CNTaian City Central Hospital · CNThe Fourth People's Hospital of Zibo City · CN

Funding

the National Natural Science Foundation of China 81602330the Natural Scientific Foundation of Shandong Province ZR2015PH056
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) are non-protein-coding transcripts shown to play important roles in tumourigenesis and tumour progression. Our study aimed to examine expression of the lncRNA MAGI2-AS3 in breast cancer and to explore its function in cancer cell growth. First, MAGI2-AS3 expression levels in clinical samples and cell lines were determined by quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The functional significance of MAGI2-AS3 in cancer cell proliferation and apoptosis was then examined in vitro. Our results showed MAGI2-AS3 to be down-regulated in breast cancer tissues compared to normal adjacent tissues. Moreover, MAGI2-AS3 markedly inhibited breast cancer cell growth and increased expression of Fas and Fas ligand (FasL). In conclusion, our data suggest that MAGI2-AS3 expression is decreased in breast cancer and that MAGI2-AS3 plays an important role as a tumour suppressor by targeting Fas and FasL signalling. These results provide new insight into novel clinical treatments for breast cancer.

Indexed as

Adaptor Proteins, Signal TransducingApoptosisBreast NeoplasmsCarrier ProteinsCell ProliferationDNA-Binding ProteinsDown-RegulationFas Ligand Proteinfas ReceptorFemaleGene ExpressionGuanylate KinasesHumansMCF-7 CellsMiddle AgedMolecular Targeted TherapyAdaptor Proteins, Signal TransducingCarrier ProteinsDNA-Binding ProteinsFASLG protein, humanFas Ligand ProteinFAS protein, humanfas ReceptorGuanylate KinasesMAGI2 protein, humanPDS5B protein, humanRNA, Long NoncodingSincalideTranscription FactorsBreast cancerFas/FasLlncRNAMAGI2-AS3Proliferation

Identifiers

PMID29679339
OpenAlexW2803095297

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.