Evidence map›Paper›PMID 40640807›Full record

ArticleCell communication and signaling : CCS2025

Neutrophil membrane-coated circular RNA nanoparticles for targeted immunotherapy in HER2-positive breast cancer brain metastasis.

Yunpeng Liu, Wei He, Xiaoju Li, Xiyan Lu, Chihua Wu, Yuan Gao, Dong Fan, Chao Dong, Huadong Zhao

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
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  4. Article
  5. Review
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  7. Review
  8. The mechanism of ncRNA in trastuzumab resistance in HER2-positive tumors.Medical oncology (Northwood, London, England) · 2025
    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.

Yunpeng Liu *The Department of Clinical Oncology, Xijing Hospital, Air Force Medical University, Xi'an, 710032, People's Republic of China.
Wei He *State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Biotechnology Center, School of Pharmacy, Air Force Medical University, Xi'an, 710032, People's Republic of China.
Xiaoju Li *Bioinformatics Center of AMMS, Beijing, 100850, P.R. China.
Xiyan LuDepartment of Outpatient, The Second Affiliated Hospital, Fourth Military Medical University, Xi'an, 710038, People's Republic of China.
Chihua WuDepartment of Breast Surgery, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Yuan GaoState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Biotechnology Center, School of Pharmacy, Air Force Medical University, Xi'an, 710032, People's Republic of China.
Dong FanDepartment of General Surgery, The Second Affiliated Hospital of the Fourth Military Medical University, Xi'an, 710038, People's Republic of China. fandong1101@126.com.
Chao DongThe Clinical Medical Research Center of Breast and Thyroid Tumor in Xinjiang, Department of Breast and Thyroid Surgery, The Affiliated Tumor Hospital of Xinjiang Medical University, Xinjiang Uygur Autonomous Region, Ürümqi, 830000, People's Republic of China. Dcdoctor@outlook.com.
Huadong ZhaoDepartment of General Surgery, The Second Affiliated Hospital of the Fourth Military Medical University, Xi'an, 710038, People's Republic of China. zhaolujy@fmmu.edu.cn.

Funding

The National Natural Science Foundation of China 82304540The National Natural Science Foundation of China 82373894The Shaanxi Provincial Natural Science Foundation 2025JC-YBMS-1063The Shaanxi Provincial Natural Science Foundation for Distinguished Young Scholars 2025JC-JCQN-097Xijing Research Foundation LHJJ2023-YX06, LHJJ24YX01
6 · The paper itself

Abstract

Breast cancer is the most prevalent malignancy worldwide, with approximately 50% of HER2-positive advanced breast cancer patients eventually developing brain metastases, significantly reducing survival. Current HER2-targeted therapies, such as trastuzumab, exhibit limited efficacy in patients with brain metastases due to poor blood-brain barrier penetration and drug resistance. This study aimed to develop a novel strategy for treating HER2-positive breast cancer brain metastases to improve overall survival. We engineered nanoparticles encapsulating circular RNA encoding the chemokine CXCL9 and an anti-PD-1 scFv, designed to target HER2-positive brain metastases. Our results demonstrate that these nanoparticles significantly enhance anti-tumor activity both in vitro and in vivo without exhibiting significant systemic toxicity. This approach improves the local tumor immune microenvironment while inducing lower systemic toxicity. In conclusion, we have established a platform of membrane-encapsulated circular RNA nanoparticles capable of targeting brain tumor lesions, showing potential for application in various brain disorders, including metastatic brain tumors. This novel approach offers a promising strategy for addressing the urgent need for effective treatments for HER2-positive breast cancer brain metastases.

Indexed as

Brain NeoplasmsBreast NeoplasmsCell MembraneErb-b2 Receptor Tyrosine KinasesImmunotherapyNanoparticlesRNA, CircularAnimalsCell Line, TumorFemaleHumansMiceERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesRNA, CircularBlood-brain barrierBrain metastasesCircular RNAHER2-positive breast cancerImmunotherapyTargeted drug deliveryTumor microenvironment

Identifiers

PMID40640807
PMCPMC12247365

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Registered trials

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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.