Evidence map›Paper›PMID 27062921›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Microrna-199a-5p Functions as a Tumor Suppressor via Suppressing Connective Tissue Growth Factor (CTGF) in Follicular Thyroid Carcinoma.

Dawei Sun, Shen Han, Chao Liu, Rui Zhou, Weihai Sun, Zhijun Zhang, Jianjun Qu

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical 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
3.7field-weighted citation impact, top 7% 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, 35 citations in OpenAlex.

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  17. BRAFV600E and RET/PTC Promote Proliferation and Migration of Papillary Thyroid Carcinoma Cells In Vitro by Regulating Nuclear Factor-κB.Medical science monitor : international medical journal of experimental and clinical research · 2017
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  18. MiR-150 Inhibits Cell Growth In Vitro and In Vivo by Restraining the RAB11A/WNT/β-Catenin Pathway in Thyroid Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2017
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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 5 institutions in 1 country.

Dawei SunThyroid Department of Affiliated Hospital of Qingdao University, Qingdao Key Laboratory of Thyroid Diseases, Qingdao, Shandong, China (mainland).
Shen Han, Guizhou Tongren Vocational and Technical College of Pharmaceutical Sciences, Guizhou, China (mainland).
Chao LiuDepartment of General Surgery, People's Hospital of Zhangqiu City, Jinan, Shandong, China (mainland).
Rui Zhou, Teaching and Research Section of Medicine and Health Management of Medical College of Qingdao University, Qingdao, Shandong, China (mainland).
Weihai SunThyroid Department of Affiliated Hospital of Qingdao University, Qingdao Key Laboratory of Thyroid Diseases, Qingdao, Shandong, China (mainland).
Zhijun Zhang, Linzi District of Zibo City People's Hospital of Hepatobiliary Surgery, Zibo, Shangdong, China (mainland).
Jianjun QuDepartment of Oncology, Weifang People's Hospital, Weifang, Shandong, China (mainland).
Qingdao University · CNAffiliated Hospital of Qingdao University · CNLinzi District People's Hospital · CNWeifang People's Hospital · CNZhangqiu City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The objective of this study was to explore the role of miR-199a-5p in the development of thyroid cancer, including its anti-proliferation effect and downstream signaling pathway. MATERIAL AND METHODS We conducted qRT-PCR analysis to detect the expressions of several microRNAs in 42 follicular thyroid carcinoma patients and 42 controls. We identified CTGF as target of miR-491, and viability and cell cycle status were determined in FTC-133 cells transfected with CTGF siRNA, miR-199a mimics, or inhibitors. RESULTS We identified an underexpression of miR-199a-5p in follicular thyroid carcinoma tissue samples compared with controls. Then we confirmed CTGF as a target of miR-199a-5p thyroid cells by using informatics analysis and luciferase reporter assay. Additionally, we found that mRNA and protein expression levels of CTGF were both clearly higher in malignant tissues than in benign tissues. miR-199a-5p mimics and CTGF siRNA similarly downregulated the expression of CTGF, and reduced the viability of FTC-133 cells by arresting the cell cycle in G0 phase. Transfection of miR-199a-5p inhibitors increased the expression of CTGF and promoted the viability of the cells by increasing the fraction of cells in G2/M and S phases. CONCLUSIONS Our study proves that the CTGF gene is a target of miR-199a-5p, demonstrating the negatively related association between CTGF and miR-199a. These findings suggest that miR-199a-5p might be a novel therapeutic target in the treatment of follicular thyroid carcinoma.

Indexed as

Adenocarcinoma, FollicularCase-Control StudiesCell Line, TumorCell ProliferationConnective Tissue Growth FactorDown-RegulationFemaleGene ExpressionGenes, Tumor SuppressorHumansMaleMicroRNAsMiddle AgedReal-Time Polymerase Chain ReactionSignal TransductionThyroid NeoplasmsCCN2 protein, humanConnective Tissue Growth FactorMicroRNAsmirn199 microRNA, human

Identifiers

PMID27062921
PMCPMC4830201
OpenAlexW2340902234

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.