Evidence map›Paper›PMID 32908453›Full record

ArticleCancer cell international2020

circRAE1 promotes colorectal cancer cell migration and invasion by modulating miR-338-3p/TYRO3 axis.

Jiabin Du, Jianhua Xu, Junxing Chen, Weinan Liu, Pengcheng Wang, Kai Ye

Abstract read
In one paragraph

Article in Cancer cell international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

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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

18 citing papers in PubMed.

  1. Article
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  9. Circ_0004585 Facilitates Tumorigenesis of Colorectal CancerCellular and molecular bioengineering · 2023
    Article
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  11. 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

6 authors.

Jiabin DuDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.
Jianhua Xu *Department of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.
Junxing ChenDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.
Weinan LiuDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.
Pengcheng WangDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.
Kai YeDepartment of Gastrointestinal Surgery, Second Affiliated Hospital of Fujian Medical University, No.950 Donghai Dajie, Fengze District, Quanzhou, 362000 Fujian China.ORCID 0000-0003-4071-5660

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGrowing evidence has revealed the involvement of circular RNAs (circRNAs) in numerous carcinogenesis. However, the role of circRNAs in the cancer biology of colorectal cancer (CRC) remains vague.

methodsQuantitative RT-PCR was used to detect the expression level of circRAE1 in CRC tissues and CRC cell lines. Cell proliferation, migration, and invasion were detected using CCK8 assay, Colony formation assay, wound-healing and Transwell assays. The interaction between circRAE1 and miR-338-3p and TRYO3 was confirmed using dual-luciferase reporter assays.

resultsWe uncovered a novel circRNA Hsa_circ_0060967 (also known as circRAE1) that was remarkably increased in CRC tissues. The high circRAE1 level was positively associated with advanced tumor stage, lymph node metastasis, and tumor size. The loss-of-function assay showed that circRAE1 accelerated cell proliferation, migration, and invasion. Besides, miR-338-3p was lowly expressed in the CRC tissues and CRC cell lines. The dual-luciferase reporter assays showed that circRAE1 could sponge miR-338-3p, which targeted TRYO3 in CRC cells. Furthermore, the overexpression of circRAE1 could rescue the impaired migration and invasion triggered by miR-338-3p mimics or si-TYRO3 in CRC cells and vice versa.

conclusionWe identified the network of circRAE1, miR-338-3p, and TYRO3 in CRC cells and determined that the increase in circRAE1 could serve as an oncogene by sponging miR-338-3p, which resulted in an upregulated TYRO3 expression. The finding suggests that circRAE1 is a potential therapeutic target and diagnostic marker for CRC treatment.

Indexed as

circRAE1circRNAsColorectal cancermiR-338-3pTYRO3

Identifiers

PMID32908453
PMCPMC7470687

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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.