AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (50.9 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article | Open Access

Ginsenoside Rg3 hydrogel in gastric cancer therapy

Fangbin Zhang1,2 ( )Yan Yan3 Xinguang Cao2 Jinping Zhang2 Yingxia Li2 Changqing Guo2 
State Key Laboratory of Metabolic Dysregulation & Prevention and Treatment of Esophageal Cancer, Division of Gastroenterology, Zhengzhou University, Zhengzhou 450052, China
Department of Gastroenterology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China
Department of Oncology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China
Show Author Information

Abstract

Gastric cancer is a major global health challenge, associated with high mortality and limited therapeutic options. Ginsenoside Rg3 (Rg3), a bioactive compound derived from ginseng, has been shown to possess significant anticancer properties, particularly through immune modulation. In this study, we explored the therapeutic potential of Ginsenoside Rg3 hydrogel in the treatment of gastric cancer, focusing on its ability to target fibroblast activation protein (FAP), a key mediator of tumor progression. Using reverse molecular docking and gene expression analysis, we identified FAP as a primary molecular target of Rg3. Preclinical evaluations revealed that Rg3 hydrogel effectively inhibited the proliferation and invasion of gastric cancer cells in vitro. Furthermore, the hydrogel promoted immunogenic cell death, resulting in a robust immune response against the tumor. Our findings suggest that Ginsenoside Rg3 hydrogel holds promise as a novel immune-based therapeutic strategy for gastric cancer, offering a potential pathway to improved clinical outcomes and treatment strategies.

Graphical Abstract

This study demonstrates that Ginsenoside Rg3-loaded Pluronic F127 (F127) hydrogel enhances tumor immunogenicity and inhibits gastric cancer progression by targeting fibroblast activation protein (FAP), offering a promising immune-based therapeutic strategy. Both in vitro and in vivo experiments confirmed the hydrogel’s ability to suppress tumor growth and promote anti-tumor immune responses.

Electronic Supplementary Material

Download File(s)
7711_ESM.pdf (1.5 MB)

References

【1】
【1】
 
 
Nano Research
Article number: 94907711

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Zhang F, Yan Y, Cao X, et al. Ginsenoside Rg3 hydrogel in gastric cancer therapy. Nano Research, 2025, 18(11): 94907711. https://doi.org/10.26599/NR.2025.94907711
Topics:

2328

Views

210

Downloads

2

Crossref

2

Web of Science

2

Scopus

0

CSCD

Received: 19 January 2025
Revised: 27 May 2025
Accepted: 20 June 2025
Published: 20 October 2025
© The Author(s) 2025. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).