Evidence map›Paper›PMID 35783017›Full record

ArticleDisease markers2022

circIFITM1/miR-802/Foxp1 Axis Participates in Proliferation and Invasion of Lovo Cells.

Yu Wan, Jinhua He, Zeping Han, Shengbo Wang, Yingying Zhao, Di Zeng, Ying Tang, Yiwei He, Lishan Zeng

Abstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Yu WanDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.ORCID https://orcid.org/0000-0003-0886-0921
Jinhua HeDepartment of Clinical Laboratory, Panyu Central Hospital, Guangzhou, China.ORCID https://orcid.org/0000-0003-4841-5179
Zeping HanDepartment of Clinical Laboratory, Panyu Central Hospital, Guangzhou, China.
Shengbo WangDepartment of Clinical Laboratory, Panyu Central Hospital, Guangzhou, China.
Yingying ZhaoDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.
Di ZengDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.
Ying TangDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.
Yiwei HeDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.
Lishan ZengDepartment of Gastroenterology, Panyu Central Hospital, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To explore the role of circIFITM1 and its potential molecular mechanism in colon cancer. Methods: The circIFITM1 in human samples and cell lines of colon cancer was measured via RT-PCR. The cyclicity of circIFITM1 was confirmed by agarose gel electrophoresis and Sanger sequencing, and the stability of circIFITM1 was confirmed by actinomycin D assay. The proliferative and invasive ability was detected by the CCK-8 assay and Transwell assay, respectively. RNA pull-down assay confirmed a combination of circIFITM1 and miRNA. Dual-luciferase reporter gene was used to detect the direct relationship between miRNA and the target gene. Results: circIFITM1 originated from the maternal gene IFITM1and had high stability. It was resistant to processing by actinomycin D. Upregulating circIFITM1 facilitated the proliferation and invasion of Lovo cells, while interfering with circIFITM1 expression inhibited them. circIFITM1 interacted with miR-802, and miR-802 targeted the 3'UTR of FOXP1. The overexpression of circIFITM1 downregulated miR-802 and upregulated FOXP1. Conclusion: circIFITM1 facilitates the proliferative and invasive abilities via miR-802/FOXP1 in Lovo cells.

Indexed as

Colonic NeoplasmsMicroRNAsCell Line, TumorCell ProliferationDactinomycinForkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessRepressor ProteinsTranscription FactorsDactinomycinForkhead Transcription FactorsFOXP1 protein, humanMicroRNAsMIRN802 microRNA, humanRepressor ProteinsTranscription Factors

Identifiers

PMID35783017
PMCPMC9249523

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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.