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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Infectious Agents and Disease

This article is part of the Research TopicZoonotic Diseases: Epidemiology, Multi-omics, and Host-pathogen Interactions Vol IIView all 12 articles

Host Angiogenic Reprogramming by Echinococcus multilocularis Protoscoleces Protein via PDGFR/PI3K/AKT Cascade

Provisionally accepted
  • 1Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases, Xinjiang Medical University, Urumqi, China
  • 2The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China

The final, formatted version of the article will be published soon.

Background: Alveolar echinococcosis (AE) is a globally present zoonotic disease globally prevalent zoonotic disease caused by Echinococcus multilocularis (E. multilocularis) infection, characterized by the formation of tumor-like growths primarily in the liver, with the potential to spread to other organs. Similar to tumors, E. multilocularis infection is accompanied by pathological angiogenesis, suggesting that the implementation of anti-angiogenic therapeutic strategies may also have promising applications in the treatment of AE. However, the mechanism of angiogenesis in AE remains unclear and has not been fully elucidated.needs to be clarified. Results: In this study, we discovered that angiogenesis related genes are significantly up-regulated in the mouse model of E. multilocularis infection and pathological angiogenesis around the lesion was significantly increased at 10-12 weeks after infection compared to the control group. Interventions utilizing a range of inhibitors at the in vitro level, including the PDGFR-β inhibitor AG1296, the PI3K inhibitor LY294002, the AKT inhibitor MK2206, and the FAK inhibitor Y15, demonstrated that E. multilocularis protoscoleces protein (EmP) induces angiogenesis through PDGFR/PI3K/AKT/FAK signaling pathway. Conclusion: Our findings provide new perspectives on how E. multilocularis infection triggers pathological angiogenesis in the host liver, and may provide a novel anti-angiogenic therapeutic strategy against E. multilocularis infection

Keywords: Echinococcus multilocularis;, pathological angiogenesis, Human Umbilical Vein Endothelial Cells, PDGF-BB, PDGFR

Received: 16 Aug 2025; Accepted: 27 Oct 2025.

Copyright: © 2025 Bi, Yang, Ke, Xue, Zhang, Liu, Chu, Li, Shao, LYU, Aji and Lin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
GUODONG LYU, lgd_xj@xjmu.edu.cn
Tuerganaili Aji, tuergan78@sina.com
Renyong Lin, renyonglin@xjmu.edu.cn

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