Evidence map›Paper›PMID 39920725›Full record

ArticleJournal of nanobiotechnology2025

Synergistic strategies for glioblastoma treatment: CRISPR-based multigene editing combined with immune checkpoint blockade.

Xiaolin Liu, Xiao Liu, Xiaonan Luo, Maorong Zhu, Nannan Liu, Juan Li, Qi Zhang, Cheng Zou, Yuxin Wu, Zhengcong Cao and 9 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
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  4. Review
  5. Extracellular Vesicle-Based Drug Delivery Systems in Cancer Therapy.International journal of molecular sciences · 2025
    Review
  6. Review
  7. 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

19 authors.

Xiaolin Liu *State Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Xiao Liu *Department of Neurosurgery, Xijing Hospital, Xi'an, China.
Xiaonan Luo *School of Basic Medicine, The Fourth Military Medical University, Xi'an, China.
Maorong Zhu *State Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Nannan LiuDepartment of Plastic and Reconstructive Surgery, Xijing Hospital, Xi'an, China.
Juan LiDepartment of Neurosurgery, Xijing Hospital, Xi'an, China.
Qi ZhangDepartment of Neurosurgery, Xijing Hospital, Xi'an, China.
Cheng ZouState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Yuxin WuState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Zhengcong CaoState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Shuangxin MaState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Weizhong WangDepartment of Neurosurgery, Xijing Hospital, Xi'an, China.
Guangzhao YangDepartment of Neurosurgery, Xijing Hospital, Xi'an, China.
Jintao GuState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Wei LiuDepartment of Neurosurgery, Xijing Hospital, Xi'an, China.
Meng LiState Key Laboratory of Cancer Biology, Biotechnology Center, School of Pharmacy, The Fourth Military Medical University, Xi'an, China.
Anan YinDepartment of Plastic and Reconstructive Surgery, Xijing Hospital, Xi'an, China. yinanan@aliyun.com.
Yalong HeDepartment of Neurosurgery, Xijing Hospital, Xi'an, China. heyl.fmmu@hotmail.com.
Wei LinDepartment of Neurosurgery, Xijing Hospital, Xi'an, China. linwei@fmmu.edu.cn.

Funding

the National Natural Science Foundation of China 82003220
6 · The paper itself

Abstract

Glioblastoma (GBM) is a primary brain tumor known for its high levels of aggressiveness and resistance to current treatments such as radiotherapy and chemotherapy. As a result, there is a pressing need for innovative therapeutic approaches to combat GBM. Thus, we have developed an engineered multifunctional extracellular vesicle (EV) delivery system that offers an "all-in-one" strategy for GBM therapy. Our approach involved the use of genetic engineering to the long-lasting production of PD-1 and the brain-specific peptide angiopep-2 on the surface of EVs. These modified EVs were then utilized to rejuvenate exhausted CD8

Indexed as

Brain NeoplasmsCRISPR-Cas SystemsGene EditingGlioblastomaImmune Checkpoint InhibitorsAnimalsB7-H1 AntigenCD8-Positive T-LymphocytesCell Cycle ProteinsCell Line, TumorExtracellular VesiclesGenetic TherapyHumansMicePolo-Like Kinase 1Programmed Cell Death 1 ReceptorB7-H1 AntigenCell Cycle ProteinsImmune Checkpoint InhibitorsPolo-Like Kinase 1Programmed Cell Death 1 ReceptorProto-Oncogene ProteinsAll-in-oneCRISPR/Cas9Gene editingGlioblastomaImmunotherapy

Identifiers

PMID39920725
PMCPMC11806770

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.