Evidence map›Paper›PMID 27347317›Full record

ArticleAmerican journal of translational research2016

Tumor-suppressive microRNA-195-5p regulates cell growth and inhibits cell cycle by targeting cyclin dependent kinase 8 in colon cancer.

Qifeng Luo, Zhenyu Zhang, Zhenling Dai, Shiva Basnet, Shuping Li, Bin Xu, Haiyan Ge

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. 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
2.6field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 41 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

7 authors at 2 institutions in 1 country.

Qifeng LuoDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Zhenyu ZhangDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Zhenling DaiDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Shiva BasnetDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Shuping LiDepartment of Research Administration, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Bin XuDepartment of General Surgery, Shanghai Tenth People's Hospital, Tongji University School of Medicine Shanghai 200072, P. R. China.
Haiyan GeDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine Shanghai 200120, P. R. China.
Shanghai East Hospital · CNShanghai Tenth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are key regulators in gene expression. Dysregulation of them in cancer development have been attracting increasing attention. The purpose of this study was to investigate the potential role of miR-195-5p in colon cancer (CC) biology. Expression of miR-195-5p in CC specimens and adjacent normal tissues were measured by quantitative polymerase chain reaction (qPCR). Overexpression of miR-195-5p was established by transfecting mimics into SW480 CC cells. Following, MTT assays, wound healing assays, invasion assays and cell cycle assays were used to explore the potential function of miR-195-5p in SW480 cells. Dual-luciferase reporter assays were performed to validate the regulation of a putative target of miR-195-5p, in corroboration with qPCR and western blot assays. The expression of miR-195-5p in CC specimens was significantly lower than that of adjacent normal tissues (P < 0.05). Overexpression of miR-195-5p inhibited cellular growth, suppressed cellular migration and invasion, and led to cell cycle arrest at G1 phase in vitro. Dual-luciferase reporter assays showed that miR-195-5p binds the 3'-untranslated region (UTR) of CDK8, suggesting that CDK8 should be a direct target of miR-195-5p. Moreover, qPCR and western blot assays confirmed CDK8 mRNA and protein levels were reduced after overexpression of miR-195-5p. These findings are supportive of miR-195-5p as a novel tumor suppressor in CC, thus may serve as a new strategy for cancer treatment.

Indexed as

CDK8cell cyclecolon cancerMiR-195-5pSW480

Identifiers

PMID27347317
PMCPMC4891422
OpenAlexW2481162415

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.