Evidence map›Paper›PMID 29628342›Full record

ArticleEBioMedicine2018

MEG3 Activated by Vitamin D Inhibits Colorectal Cancer Cells Proliferation and Migration via Regulating Clusterin.

Yan Zhu, Peizhan Chen, Yisha Gao, Na Ta, Yunshuo Zhang, Jialin Cai, Yong Zhao, Shupeng Liu, Jianming Zheng

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.6field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 88 citations in OpenAlex.

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  12. The role and function of CLU in cancer biology and therapy.Clinical and experimental medicine · 2023
    Review
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  15. Article
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  18. Long non-coding RNAs involved in different steps of cancer metastasis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Yan ZhuDepartment of Pathology, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China.
Peizhan ChenTranslational Medicine Research Center, Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Shanghai 201821, PR China.
Yisha GaoDepartment of Pathology, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China.
Na TaDepartment of Pathology, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China.
Yunshuo ZhangDepartment of Pathology, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China.
Jialin CaiTranslational Medicine Research Center, Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, Shanghai 201821, PR China.
Yong ZhaoOffice of Shanghai Administrative Committee for Laboratory Animal, Shanghai, Laboratory Animals Research Center, Shanghai, 201203, PR China.
Shupeng LiuClinical Research Center, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China. Electronic address: lshu_p@aliyun.com.
Jianming ZhengDepartment of Pathology, Changhai Hospital, Secondary Military Medical University, Shanghai 200433, PR China. Electronic address: jmzheng1962@163.com.
Second Military Medical University · CNShanghai Jiao Tong University · CNShanghai Veterinary Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long non-coding RNA maternally expressed gene 3 (MEG3) is frequently dysregulated in human cancers; however, its roles in colorectal cancer (CRC) development are largely unknown. Here, we reported that MEG3 was down-regulated in CRC tissues and CRC patients with lower MEG3 showed poorer overall survival and disease-free survival than those with higher MEG3 level. MEG3 over-expression represses CRC cells proliferation and migration in vivo and in vitro, while MEG3 knockdown leads to the enhanced proliferation and metastasis of CRC cells. In CRC cells, MEG3 over-expression is related to decreased Clusterin mRNA and the corresponding protein levels, and it also directly binds to Clusterin protein through its 732-1174 region. In further, Clusterin over-expression rescues the compromised abilities of proliferation and metastasis induced by MEG3 over-expression, suggesting that MEG3 inhibits the CRC progression through regulating the Clusterin activities. Additionally, we found that 1α,25-(OH)

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationClusterinColorectal NeoplasmsDisease-Free SurvivalGene Expression Regulation, NeoplasticHumansMaleMice, Inbred BALB CMice, NudeNeoplasm MetastasisPrognosisPromoter Regions, GeneticProtein BindingClusterinMEG3 non-coding RNA, humanRNA, Long NoncodingVitamin DClusterinCRClncRNAMEG3Vitamin D

Identifiers

PMID29628342
PMCPMC5952405
OpenAlexW2795199023

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.