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 (12.1 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review Article | Open Access

Nanomedicine-enabled epigenetic therapy for glioblastoma: Overcome the blood-brain barrier and therapeutic resistance

Qingxin Yang1,2,7,§Yuan Zhong2,3,§Shaoyu Cai7Zenghua Sheng2,6Da Sun2,5Peixing Chen1Yuanyuan Zhang1Jianshu Li2,4 ( )Wei Wu2,3 ( )Maolan Zhang1,2 ( )
Chongqing Engineering Laboratory for Nano-Micro Biomedical Testing Technology, Chongqing University of Science and Technology, Chongqing 401331, China
Jin Feng Laboratory, Chongqing 401329, China
Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing 400044, China
College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu 610065, China
Institute of Life Sciences & Biomedical Collaborative Innovation Center of Zhejiang Province, Wenzhou University, Wenzhou 325035, China
Department of Oncology, Jiangjin Hospital, School of Medicine, Chongqing University, Chongqing 402260, China
School of Chemistry and Chemical Engineering, Chongqing University of Science and Technology, Chongqing 401331, China

§ Qingxin Yang and Yuan Zhong contributed equally to this work.

Show Author Information

Abstract

Glioblastoma (GBM), the most aggressive grade IV malignant tumor in the central nervous system, presents a poor prognosis. Despite extensive insights into its molecular pathology, the conventional Stupp regimen remains largely ineffective due to several factors, including diffuse tumor infiltration, radioresistance, the blood-brain barrier (BBB), and therapy resistance driven by GBM stem cells (GSCs). Research has established that epigenetic modifications play a crucial role in the initiation, progression, invasion, and treatment resistance of GBM. However, existing epigenetic modulators frequently encounter pharmacokinetic limitations, which significantly compromise their efficacy. As a result, there is an urgent need for novel technologies to enhance the therapeutic impact of epigenetic modulators in GBM. This article reviews and discusses current GBM treatments, with a particular emphasis on the rapidly evolving strategy of nanomedicine. By encapsulating epigenetic modulators in precisely engineered nanocarriers, this approach not only improves drug solubility, stability, and circulation time, but also enhances tumor accumulation through passive or active targeting strategies, while allowing for controlled and intelligent drug release. Importantly, specially designed nanocarrier systems can effectively cross the BBB and overcome drug resistance, paving the way for new drug delivery methods in the management of GBM.

Graphical Abstract

This review discusses current glioblastoma (GBM) treatments, focusing on nanomedicine. Encapsulating epigenetic modulators in nanocarriers improves drug solubility, stability, and circulation time. It enhances tumor accumulation via passive/active targeting and enables controlled drug release. Notably, these systems can cross the blood-brain barrier (BBB) and overcome drug resistance, offering promising new delivery methods for GBM therapy.

References

【1】
【1】
 
 
Nano Research
Article number: 94908472

{{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:
Yang Q, Zhong Y, Cai S, et al. Nanomedicine-enabled epigenetic therapy for glioblastoma: Overcome the blood-brain barrier and therapeutic resistance. Nano Research, 2026, 19(5): 94908472. https://doi.org/10.26599/NR.2026.94908472
Topics:

1755

Views

260

Downloads

2

Crossref

2

Web of Science

2

Scopus

0

CSCD

Received: 18 November 2025
Revised: 16 January 2026
Accepted: 21 January 2026
Published: 24 March 2026
© The Author(s) 2026. 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/).