Evidence map›Paper›PMID 33640021›Full record

ArticleJournal of biological research (Thessalonike, Greece)2021

CircCTNNA1 acts as a ceRNA for miR-363-3p to facilitate the progression of colorectal cancer by promoting CXCL5 expression.

Yan Zhang, Sheng Zheng, Nansheng Liao, Huifeng Huang, Wenxiao Chen, Zhenxing Wu, Deqing Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of biological research (Thessalonike, Greece), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  4. Role of microRNA-363 during tumor progression and invasion.Journal of physiology and biochemistry · 2024
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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

7 authors at 3 institutions in 1 country.

Yan Zhang *Department of Gastroenterology, Taizhou First People's Hospital, Taizhou, 318020, China.
Sheng Zheng *Department of Gastroenterology, The Third People's Hospital of Yunnan Province, Kunming, 650011, China.
Nansheng LiaoDepartment of General Surgery, Taizhou First People's Hospital, Taizhou, 318020, China.
Huifeng HuangDepartment of Gastroenterology, Taizhou First People's Hospital, Taizhou, 318020, China.
Wenxiao ChenDepartment of Gastroenterology, Taizhou First People's Hospital, Taizhou, 318020, China.
Zhenxing WuDepartment of Gastroenterology, Taizhou First People's Hospital, Taizhou, 318020, China.
Deqing WuDepartment of Gastrointestinal Surgery, Guangdong Academy of Medical Sciences, School of Medicine, Guangdong Provincial People's Hospital, South China University of Technology, No. 106 Zhongshan 2nd Road, Yuexiu District, Guangzhou, 510000, China. qymqcb@163.com.
Taizhou First People's Hospital · CNGuangdong Provincial People's Hospital · CNThird People's Hospital of Yunnan Province · CN

Funding

Basic Research Joint Special General Project of Yunnan Provincial Local Universities (part) 018FH001-076Basic Research Joint Special General Project of Yunnan Provincial Local Universities (part) 2018FH001-080Yunnan Province high-level Health and Family planning Personnel Training Project Yunwei Science and Education Development [2017] No. 14
6 · The paper itself

Abstract

backgroundCircular RNAs (circRNA) have been shown to be involved in the pathogenesis of colorectal cancer (CRC). CircCTNNA1 was found to be one of the upregulated circRNAs in CRC. However, there are few studies on circCTNNA1, so it is necessary to carry out further studies.

methodsThe expression of circCTNNA1, microRNA (miR)-363-3p, and chemokine C-X-C motif ligand 5 (CXCL5) was detected by quantitative real-time PCR (qRT-PCR). The protein levels of CXCL5 and metastasis markers were measured using western blot (WB) analysis. Cell proliferation, apoptosis, cell cycle, migration, and invasion were determined by cell counting kit 8 (CCK8) assay, colony formation assay, flow cytometry, and transwell assay. The relationship between miR-363-3p and circCTNNA1 or CXCL5 was evaluated via dual-luciferase reporter assay and RNA immunoprecipitation assay. Animal study was performed to explore the function of circCTNNA1 on CRC tumorigenesis.

resultsCircCTNNA1 and CXCL5 were highly expressed in CRC. Knockdown of circCTNNA1 could inhibit the proliferation, cell cycle, metastasis, and promote the apoptosis of CRC cells. MiR-363-3p could be sponged by circCTNNA1, and the inhibition effect of circCTNNA1 silencing on CRC progression could be reversed by miR-363-3p inhibitor. Moreover, miR-363-3p could interact with CXCL5, and CXCL5 overexpression also could reverse the suppressive effect of miR-363-3p on CRC progression. Downregulation of circCTNNA1 also could hinder the tumor growth of CRC in vivo.

conclusionCircCTNNA1 enhanced CRC progression via regulating the miR-363-3p/CXCL5 axis.

Indexed as

circCTNNA1Colorectal cancerCXCL5miR-363-3p

Identifiers

PMID33640021
PMCPMC7913448
OpenAlexW3134466903

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.