Evidence map›Paper›PMID 36797792›Full record

ArticleParasites & vectors2023

Clonorchis sinensis legumain promotes migration and invasion of cholangiocarcinoma cells via regulating tumor-related molecules.

Yanfei Chu, Doufei Shi, Nan Wang, Lebin Ren, Naiguo Liu, Fengai Hu, Wei Meng, Sung-Jong Hong, Xuelian Bai

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

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  8. The cancer microbiome.Advances in clinical chemistry · 2025
    Review
  9. RETRACTED: PTEN Deficiency Induced by Extracellular Vesicle miRNAs fromInternational journal of molecular sciences · 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

9 authors at 2 institutions in 2 countries.

Yanfei Chu *Clinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Doufei Shi *Department of Geriatric Medicine, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Nan WangClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Lebin RenClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Naiguo LiuClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Fengai HuClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Wei MengClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China.
Sung-Jong HongDepartment of Medical Environmental Biology, Chung-Ang University College of Medicine, Dongjak-Gu, Seoul, 156-756, Republic of Korea.
Xuelian BaiClinical Medicine Laboratory, Binzhou Medical University Hospital, Binzhou, 256603, Shandong, People's Republic of China. xuelianbai99@163.com.
Binzhou Medical University · CNChung-Ang University · KR

Funding

Binzhou Medical University science project BY2017KYQD12Shandong Medicine and Health Technology Project 2017WS884Shandong Natural Science Foundation ZR2022MH141
6 · The paper itself

Abstract

backgroundClonorchis sinensis infection causes serious pathological changes in the bile duct and is highly correlated with cholangiocarcinoma. The excretory-secretory products (ESP) of C. sinensis play a critical role in the oncogenesis and progression of cholangiocarcinoma, while the components and precise mechanism remain unclear. Here, we evaluated the function of C. sinensis legumain (Cslegumain) in promoting the invasion and migration of cholangiocarcinoma cells and the mechanism involved.

methodsThe structural and molecular characteristics of Cslegumain were predicted and analyzed using the online program Phyre2. Quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemical staining were performed to test the transcriptional level of Cslegumain and its localization in the adult. Native Cslegumain was detected by western blotting assay. The effects of Cslegumain on the proliferation, invasion and migration of cholangiocarcinoma cells were checked using CCK-8 assay, Matrigel transwell assay and scratch wound healing assay. Expression levels of tumor-related molecules regulated by Cslegumain were evaluated by qRT-PCR and western blotting assay.

resultsCslegumain showed high similarity with human legumain in the secondary and tertiary structures and displayed higher transcriptional levels in the adult worm than in the metacercariae. Native Cslegumain was detected in a catalytic form and was localized mainly in the intestine of the C. sinensis adult and epithelial cells of the intrahepatic bile duct. After transfection into RBE cells, Cslegumain showed high ability in promoting the invasion and migration but not the proliferation of cholangiocarcinoma RBE cells. Furthermore, the expression levels of some molecules including E-cadherin and N-cadherin were downregulated, while the levels of α-actinin 4, β-catenin and inducible nitric oxide synthase (iNOS) were upregulated.

conclusionsOur findings indicated that Cslegumain showed very similar structures as those of human legumain and could promote the invasion and migration of cholangiocarcinoma cells by regulating some tumor-related molecules.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaClonorchis sinensisAnimalsAsparaginyl EndopeptidaseBile Ducts, IntrahepaticCell ProliferationHumansAsparaginyl EndopeptidaseCholangiocarcinomaClonorchis sinensisCslegumainMigration and invasion

Identifiers

PMID36797792
PMCPMC9933405
OpenAlexW4321092874

What OpenQuestion holds

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LicenceCC BY
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.