Evidence map›Paper›PMID 39466826›Full record

ArticlePLoS neglected tropical diseases2024

Extracellular vesicles of Clonorchis sinensis promote the malignant phenotypes of cholangiocarcinoma via NF-κB/EMT axis.

Xiaowen Pan, Qing He, Yingxuan Yin, Anyuan Xu, Aoxun Wu, Xueqing Yi, Zifeng Zhong, Yinjuan Wu, Xuerong Li

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Food and waterborne parasitology · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
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.

Xiaowen PanDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Qing HeDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Yingxuan YinDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Anyuan XuDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Aoxun WuDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Xueqing YiDepartment of Basic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China.
Zifeng ZhongDepartment of Basic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China.
Yinjuan WuDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Xuerong LiDepartment of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-5518-1617

Funding

Guangzhou Municipal Science and Technology Project 202201011723National Key Research and Development Program of China 2021YFC2300800Natural Science Foundation of Guangdong Province 2023A1515010955Sun Yat-sen Creative Project 202310706
6 · The paper itself

Abstract

Clonorchis sinensis infection is an important risk factor for cholangiocarcinoma (CCA). It has been reported that extracellular vesicles (EVs) are involved in the parasite-host interaction, and EVs of C. sinensis (CsEVs) can contribute to biliary injuries and inflammation. However, uncertainty surrounds the function of CsEVs in the progression of CCA. In this study, differential ultracentrifugation was used to separate CsEVs from the culture supernatant of C. sinensis adult worms, and they were then identified by transmission electron microscopy, nanoparticle tracking analysis and proteome assays. CCK8, EdU-488 and colony formation assays were used to explore the effect of CsEVs on the proliferation of CCA cells in vitro. Wound healing assays, transwell assays and in vivo lung metastasis model were conducted to evaluate the migration and invasion abilities. Moreover, the involvement of EMT process, as well as NF-κB and ERK signaling pathway was assessed. Results showed that CsEVs were successfully isolated and could be taken up by CCA cells, which promoted proliferation by accelerating cell cycle progression. In addition, CsEVs could facilitate cell metastasis by triggering the epithelial-mesenchymal transition (EMT). Mechanistically, activation of NF-κB signaling pathway was involved in the CsEVs-mediated EMT, which could be reversed partly by BAY 11-7082 (an inhibitor of NF-κB). In conclusion, these findings suggested that CsEVs could induce the aberrant proliferation and metastasis of CCA cells by stimulating the NF-κB/EMT axis, providing a novel theoretical explanation for liver fluke-associated CCA.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaClonorchis sinensisExtracellular VesiclesSignal TransductionAnimalsCell Line, TumorCell MovementCell ProliferationClonorchiasisEpithelial-Mesenchymal TransitionHumansMaleMiceNF-kappa BPhenotypeNF-kappa B

Identifiers

PMID39466826
PMCPMC11516169

What OpenQuestion holds

Textmetadata
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.