Evidence map›Paper›PMID 36192575›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2023

C5aR1 promotes the progression of colorectal cancer by EMT and activating Wnt/β-catenin pathway.

Duo Xu, Meirong Li, Longyan Ran, Xiaochen Li, Xingwang Sun, Tao Yin

Open access · hybridAbstract read
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Duo Xu *College of Basic Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Meirong Li *Department of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Longyan RanCollege of Basic Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Xiaochen LiCollege of Basic Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Xingwang SunDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Tao YinDepartment of Pathology, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China. yintao1745@swmu.edu.cn.ORCID http://orcid.org/0000-0001-5735-9389
Southwest Medical University · CNAffiliated Hospital of Southwest Medical University · CN

Funding

Major cultivation project of Education Department of Sichuan Province NO. 18CZ0044PhD Research Fund of the Affiliated Hospital of Southwest Medical University NO. 16241
6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is one of the most common malignant cancers in human, and its incidence increases gradually every year. Metastasis is an important factor leading to tumor development. The epithelial-mesenchymal transition (EMT) has been proved to be closely related to tumor metastasis, yet its related mechanism in CRC remains to be explored.

methodsWe obtained the differentially expressed gene C5aR1 with SETDB1 stable overexpression and knockdown cells by RNA-seq. Cell proliferation was tested by CCK8 and colony formation assay. Migration and invasion of CRC cells were determined by the wound healing and transwell invasion assay. The potential pathway of C5aR1 in CRC was preliminarily studied by western blotting.

resultsSequencing results showed that C5aR1 was the most differentially expressed gene. By changing the expression of C5aR1 in CRC cells, this study found that C5aR1 promoted the proliferation, colony formation, migration and invasion of CRC cells in vitro. C5aR1 accelerated the EMT process and the expression of C5aR1 altered the molecular expression of key proteins in the Wnt/β-catenin pathway.

conclusionC5aR1 promotes the development of CRC and accelerates the EMT process. Furthermore, C5aR1 may involve in the regulation of Wnt/β-catenin pathway in CRC.

Indexed as

Colorectal NeoplasmsEpithelial-Mesenchymal TransitionReceptor, Anaphylatoxin C5aWnt Signaling Pathwaybeta CateninCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansbeta CateninC5AR1 protein, humanReceptor, Anaphylatoxin C5aC5aR1CRCEMTRNA-seqWnt/β-catenin

Identifiers

PMID36192575
PMCPMC9873742
OpenAlexW4300817391

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.