Evidence map›Paper›PMID 27811858›Full record

ArticleBritish journal of cancer2016

The FOXD3/miR-214/MED19 axis suppresses tumour growth and metastasis in human colorectal cancer.

G Y He, J L Hu, L Zhou, X H Zhu, S N Xin, D Zhang, G F Lu, W T Liao, Y Q Ding, L Liang

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 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, 47 citations in OpenAlex.

  1. Article
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  5. The role of mediator complex subunit 19 in human diseases.Experimental biology and medicine (Maywood, N.J.) · 2021
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  14. MiRNA505/NET1 Axis Acts as a CD8OncoTargets and therapy · 2020
    Article
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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 2 institutions in 1 country.

G Y HeDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
J L HuDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
L ZhouFirst School of Clinical Medicine, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
X H ZhuDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
S N XinDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
D ZhangDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
G F LuDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
W T LiaoDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
Y Q DingDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
L LiangDepartment of Pathology, Southern Medical University, Guangzhou city 510515, Guangdong Province, China.
Southern Medical University · CNKey Laboratory of Guangdong Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMiR-214 is aberrantly regulated in several tumours, but its underlying mechanisms in colorectal cancer (CRC) metastasis remain largely unknown. This study aimed to demonstrate the function and potential mechanism of miR-214 in regulating invasion and metastasis of CRC.

methodsThe transcription factor and targets of miR-214 were predicted by bioinformatics and validated using ChIP and dual-luciferase reporter assay. DNA methylation status was explored using bisulphite sequencing PCR. The in vitro and in vivo function of miR-214 in CRC was evaluated using MTT, plate colony formation, Matrigel invasion and animal models. Real-time PCR or western blotting was performed to detect FOXD3, miR-214 and MED19 expressions in CRC cells and clinical specimens.

resultsMiR-214 was downregulated in CRC and was significantly correlated with lymphatic metastasis. Downregulation of miR-214 might due to promoter hypermethylation in CRC. FOXD3 was validated as a transcription factor of miR-214 by ChIP assay. Dual-luciferase assay identified MED19 as a target of miR-214 in CRC. In vitro and in vivo experiments showed that miR-214 mediated the inhibiting effect of FOXD3 on proliferation, invasion and metastasis by targeting MED19. Spearman's correlation analysis showed a positive correlation between FOXD3 and miR-214, and negative correlations between FOXD3 and MED19, miR-214 and MED19 in CRC cells and clinical specimens.

conclusionsFOXD3/miR-214/MED19 axis is important for the regulation of growth, invasion and metastasis of CRC. Targeting the miR-214-mediated axis might be helpful for the treatment of CRC.

Indexed as

AnimalsCell Line, TumorCell ProliferationColorectal NeoplasmsDNA MethylationDNA PrimersForkhead Transcription FactorsGene SilencingHumansMediator ComplexMiceMice, Inbred BALB CMice, NudeMicroRNAsNeoplasm MetastasisDNA PrimersForkhead Transcription FactorsFOXD3 protein, humanMED19 protein, humanMediator ComplexMicroRNAsMIRN214 microRNA, human

Identifiers

PMID27811858
PMCPMC5129822
OpenAlexW2548936049

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.