Evidence map›Paper›PMID 28784723›Full record

ArticleMolecular and cellular biology2017

Upregulation of MicroRNA 18b Contributes to the Development of Colorectal Cancer by Inhibiting CDKN2B.

Yiming Li, Meng Chen, Juan Liu, Lianyun Li, Xiao Yang, Jiao Zhao, Min Wu, Mei Ye

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  8. mRNA and miRNA Expression Analyses of theInternational journal of molecular sciences · 2021
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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

8 authors at 3 institutions in 1 country.

Yiming LiGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Meng ChenGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Juan LiuGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Lianyun LiCollege of Life Sciences, Wuhan University, Wuhan, Hubei, China.
Xiao YangGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Jiao ZhaoGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Min WuCollege of Life Sciences, Wuhan University, Wuhan, Hubei, China.
Mei YeGastroenterology Division, Integrated Internal Medicine and Geriatrics Department, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China wumeiye08@163.com.
Wuhan University · CNZhongnan Hospital of Wuhan University · CNHubei Provincial Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) exhibit aberrant expression in the initiation and progression of a variety of human cancers, including colorectal cancer (CRC). However, the exact mechanisms are not well defined. miRNA expression profiles were characterized by microarrays in CRC samples, and miRNA 18b (miR-18b) was increased significantly in tumor tissues. The expression of miR-18b was confirmed in the CRC cell lines SW480 and HCT116 and 44 clinical specimens by quantitative real-time PCR (qRT-PCR). Multiple linear regression analysis showed a strong correlation of miR-18b expression with lymph node and distant metastasis. Overexpression of miR-18b promoted cell proliferation by facilitating cell cycle progression, and knockdown of miR-18b significantly suppressed migration in CRC cells. CDKN2B was identified as a target of miR-18b by high-throughput RNA sequencing and bioinformatics. After transfection with a miR-18b mimic, expression of CDKN2B was reduced significantly in CRC cells, and the effect was restored when a miR-18b inhibitor was transfected. A luciferase assay indicated miR-18b directly binds to the 3' untranslated region (UTR) of CDKN2B. Expression of CDKN2B was downregulated in patient cancer tissues and negatively correlated with miR-18b. In a model of ectopic expression of miR-18b and CDKN2B, CDKN2B overexpression antagonized the effects of miR-18b

Indexed as

Up-Regulation3' Untranslated RegionsAnimalsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsCyclin-Dependent Kinase Inhibitor p15FemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansLymphatic MetastasisMaleMiceMicroRNAs3' Untranslated RegionsCdkn2b protein, mouseCyclin-Dependent Kinase Inhibitor p15MicroRNAsMIRN18 microRNA, humanCDKN2Bcolorectal cancerhigh-throughput RNA sequencingmicroRNA 18bmicroRNA array

Identifiers

PMID28784723
PMCPMC5660464
OpenAlexW2743923431

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.