Evidence map›Paper›PMID 30253791›Full record

ArticleJournal of experimental & clinical cancer research : CR2018

MiR-452 promotes an aggressive colorectal cancer phenotype by regulating a Wnt/β-catenin positive feedback loop.

Tingting Li, Xiangyu Jian, Han He, Qiuhua Lai, Xianzheng Li, Danling Deng, Tengfei Liu, Jiehong Zhu, Hongli Jiao, Yaping Ye and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Function and mechanisms of microRNA-20a in colorectal cancer.Experimental and therapeutic medicine · 2020
    Review
  16. Article
  17. The miRNAs Role in Melanoma and in Its Resistance to Therapy.International journal of molecular sciences · 2020
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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

15 authors at 4 institutions in 1 country.

Tingting LiDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Xiangyu JianDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Han HeDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Qiuhua LaiDepartment of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Xianzheng LiMedical genetic center, Guangdong Women and Children Hospital, Guangzhou, Guangdong, China.
Danling DengDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Tengfei LiuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Jiehong ZhuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Hongli JiaoDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Yaping YeDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Shuyang WangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Minhui YangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Lin ZhengDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Weijie ZhouDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China. 30269940@qq.com.
Yanqing DingDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China. dyq20184@126.com.
Southern Medical University · CNGuangzhou Experimental Station · CNNanfang Hospital · CNGuangdong Province Women and Children Hospital · CN

Funding

Guangdong Provincial medical scientific research Foundation of China A2016218Guangdong Provincial Natural Science Foundation of China No. 2017A030313707, 2016A030310394, 2017A030313463, 2017A030313643, 2017A030313583, 2017A030310081, 2017A030310117, 2017C1034229, 2016A030310394, 2016A030310392, 2016A030310395, 2015A030306048, 2014A030310134Guangzhou Science & Technology Plan Project 201300000056Key Program of National Natural Science Foundation of Guangdong, China 2010B031500012National Basic Research Program of China 973 program, 2015CB554002National Natural Science Foundation of China National Natural Science Foundation of ChinaPresidents fund of Nanfang Hospital 2015C009
6 · The paper itself

Abstract

backgroundAberrant activation of Wnt/β-catenin signaling pathway is considered to be an important issue in progression and metastasis of various human cancers, especially in colorectal cancer (CRC). MiR-452 could activate of Wnt/β-catenin signaling. But the mechanism remains unclear.

methodsThe expression of miR-452 in CRC and normal tissues was detected by real-time quantitative PCR. The effect of miR-452 on CRC growth and invasion was conducted by functional experiments in vitro and in vivo. Bioinformatics and cell luciferase function studies verified the direct regulation of miR-452 on the 3'-UTR of the GSK3β, which leads to the activation of Wnt/β-catenin signaling.

resultsMiR-452 was upregulated in CRC compared with normal tissues and was correlated with clinical significance. The luciferase reporter system studies affirmed the direct regulation of miR-452 on the 3'-UTR of the GSK3β, which activate the Wnt/β-catenin signaling. The ectopic upregulation of miR-452 significantly inhibited the expression of GSK3β and enhanced CRC proliferation and invasion in vitro and in vivo. Meanwhile, knockdown of miR-452 significantly recovered the expression of GSK3β and attenuated Wnt/β-catenin-mediated cell metastasis and proliferation. More important, T-cell factor/lymphoid enhancer factor (TCF/LEF) family of transcription factors, which are crucial downstream molecules of the Wnt/β-catenin signaling pathway was verified as a valid transcription factor of miR-452's promoter.

conclusionsOur findings first demonstrate that miR-452-GSK3β-LEF1/TCF4 positive feedback loop induce CRC proliferation and migration.

Indexed as

AdultAgedAnimalsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlycogen Synthase Kinase 3 betaHCT116 CellsHumansLymphoid Enhancer-Binding Factor 1MaleMiceGlycogen Synthase Kinase 3 betaLEF1 protein, humanLymphoid Enhancer-Binding Factor 1MicroRNAsMIRN452 microRNA, humanTCF4 protein, humanTranscription Factor 4Colorectal canerGSK3βmiR-452TCF4/LEF1Wnt/β-catenin pathway

Identifiers

PMID30253791
PMCPMC6156870
OpenAlexW2892923684

What OpenQuestion holds

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Registered trials

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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.