Evidence map›Paper›PMID 32406388›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2020

miR-20a/Foxj2 Axis Mediates Growth and Metastasis of Colorectal Cancer Cells as Identified by Integrated Analysis.

Yong Qiang, Liang Feng, Gang Wang, Jian Liu, Jing Zhang, Lanlan Xiang, Chunjie Su, Songbai Zhang, Xiongwei Xie, Erlin Chen

Open access · greenAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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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

10 authors at 3 institutions in 1 country.

Yong QiangDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Liang FengDepartment of Burn and Plastic Surgery, Affiliated Nantong Hospital No. 3 of Nantong University, Nantong, Jiangsu, China (mainland).
Gang WangDepartment of Anesthesiology, Union Hospital Affiliated with Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, China (mainland).
Jian LiuDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Jing ZhangDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Lanlan XiangDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Chunjie SuDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Songbai ZhangDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Xiongwei XieDepartment of General Surgery, Jingmen No. 1 People's Hospital, Jingmen, Hubei, China (mainland).
Erlin ChenDepartment of General Surgery, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China (mainland).
First People’s Hospital of Jingmen · CNNantong University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND MicroRNAs (miRNAs) have a significant regulatory effect on the proliferation, migration, and invasion of cells, and have been widely reported to have oncogenic or tumor-suppressive impacts on various tumors. In the present study we assessed the regulation and function of miR-20a on colorectal cancer (CRC) cell lines. MATERIAL AND METHODS qPCR was used to quantify miR-20a expression. Luciferase reporter assay was conducted to confirm Foxj2 3'UTR associations. In addition, the function of miR-20a and Foxj2 in CRC was detected using MTT, colony formation, transwell assays, and cell cycle analysis. RESULTS Our data revealed that miR-20a expression was elevated in the CRC cell lines, and cell migration, proliferation, and invasion abilities were promoted by the overexpression of miR-20a. Moreover, Foxj2 was authenticated as a direct target gene of miR-20a in CRC cells. Furthermore, we found that the ectopic Foxj2 dramatically suppressed miR-20a-promoted proliferation, migration, invasion, and xenografts in vitro and in vivo, and induced cell cycle arrest at G1 stage. CONCLUSIONS Our results showing the roles of miR-20a/Foxj2 in carcinogenesis of CRC may help improve treatment of CRC.

Indexed as

Cell Line, TumorCell MovementCell ProliferationChinaColorectal NeoplasmsEpithelial-Mesenchymal TransitionForkhead Transcription FactorsGene ExpressionGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisForkhead Transcription FactorsFOXJ2 protein, humanMicroRNAsMIRN20a microRNA, human

Identifiers

PMID32406388
PMCPMC7247419
OpenAlexW3021338335

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.