Evidence map›Paper›PMID 30867751›Full record

ArticleOncology letters2019

MicroRNA-218 inhibits the cell proliferation and migration in clear cell renal cell carcinoma through targeting cancerous inhibitor of protein phosphatase 2A.

Ruojing Wei, Xiongjun Ye, Yawei Zhao, Ning Jia, Tongwei Liu, Wenfeng Lian, Hongjian Wei, Gang Zhang, Lijie Song

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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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 3 institutions in 1 country.

Ruojing WeiDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Xiongjun YeDepartment of Urological Surgery, Beijing University People's Hospital, Beijing 100044, P.R. China.
Yawei ZhaoDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Ning JiaDepartment of Digestive Endoscopy Center, The Affiliated Hospital of Hebei University, Baoding, Hebei 071000, P.R. China.
Tongwei LiuDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Wenfeng LianDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Hongjian WeiDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Gang ZhangDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Lijie SongDepartment of Urology, The First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.
Baoding People's Hospital · CNAffiliated Hospital of Hebei University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRs) have emerged as critical modulators of tumor initiation and progression in numerous types of human cancer, including clear cell renal cell carcinoma (ccRCC), which is the most common subtype of renal cell carcinoma. Cancerous inhibitor of protein phosphatase 2A (CIP2A) is a newly characterized oncoprotein and its overexpression has been reported to promote cellular epithelial-mesenchymal transition and the tumor progression of ccRCC. The present study examined the effects of miR-218 on CIP2A expression in ccRCC cells. The results demonstrated that the expression level of miR-218 was lower in ccRCC tissues compared with that in adjacent non-tumor renal tissues. In addition, it was identified that miR-128 could directly bind to the 3'-untranslated region of CIP2A. Furthermore, a negative correlation between the expression levels of miR-218 and CIP2A was detected in ccRCC. Additionally, the downregulation of CIP2A or overexpression of miR-218 in ccRCC cells was revealed to inhibit cell proliferation and migration. In summary, these data suggest that miR-218 serves a role in the regulation of CIP2A and elucidate its consequences on tumor progression, tumor cell proliferation and migration. These results indicate that miR-218 may exhibit potential as a molecular target for the treatment of ccRCC.

Indexed as

cancerous inhibitor of protein phosphatase 2Aclear cell renal cell carcinomamicroRNA-218tumor suppressor

Identifiers

PMID30867751
PMCPMC6396187
OpenAlexW2914038348

What OpenQuestion holds

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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.