Evidence map›Paper›PMID 40542894›Full record

ArticleAnalytical and bioanalytical chemistry2025

Direct SERS profiling of small extracellular vesicles in cerebrospinal fluid for pediatric medulloblastoma detection and treatment monitoring.

Guangxia Shao, Ruoping Chen, Minghui Li, Yujie Liu, Kun Zhang, Qijia Zhan

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Article in Analytical and bioanalytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Guangxia ShaoDepartment of Neurosurgery, Children's Hospital of Shanghai, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.
Ruoping ChenDepartment of Neurosurgery, Children's Hospital of Shanghai, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China.
Minghui LiShanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai Institute of Pediatric Research , Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China.
Yujie LiuShanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai Institute of Pediatric Research , Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China.
Kun ZhangShanghai Key Laboratory of Pediatric Gastroenterology and Nutrition, Shanghai Institute of Pediatric Research , Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China. kunzhang@shsmu.edu.cn.ORCID http://orcid.org/0000-0001-8759-7636
Qijia ZhanDepartment of Neurosurgery, Children's Hospital of Shanghai, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200062, China. hanbing_1125@163.com.

Funding

the National Natural Science Foundation of China 21974088the Science and Technology Commission of Shanghai Municipality 21ZR1481300
6 · The paper itself

Abstract

Definitive diagnosis of intracranial tumors by less-invasive approaches provides diagnostic information to facilitate personalized treatment decisions and avoid unnecessary invasive biopsy operations. However, it remains challenging, largely due to a lack of reliable molecular biomarkers. Here, we demonstrated that molecular profiles of small extracellular vesicles (sEVs) in cerebrospinal fluid (CSF) decoded by surface-enhanced Raman spectroscopy (SERS) revealed highly specific signatures to detect and accurately discriminate common primary intracranial tumors in children that can be challenging to distinguish using standard-of-care imaging. Specifically, the fabrication of silver nanocube-based three-dimensional SERS substrates enabled the acquisition of highly resolved Raman spectra of sEVs in clinical CSF samples. The development of stacking machine learning frameworks to analyze the Raman data sets unveiled differential vibrational modes and generated high accuracy for diagnosing pediatric medulloblastoma (MB), the most common malignant brain tumor in children, with an area under the receiver operating characteristic curve (AUC(ROC)) of 0.963. Furthermore, we observed high discriminative capacity of our Raman spectral classifier to distinguish MB from other brain tumors (AUC(ROC) = 0.906). Finally, we showed that dynamic analysis of the CSF sEV Raman profiles allowed monitoring of the therapeutic response of MB at the molecular level. Our study holds promise for facilitating precision medicine in brain tumors.

Indexed as

Cerebellar NeoplasmsExtracellular VesiclesMedulloblastomaSpectrum Analysis, RamanAdolescentBiomarkers, TumorChildChild, PreschoolFemaleHumansMaleSilverBiomarkers, TumorSilverCerebrospinal fluidExosomesLiquid biopsyMedulloblastomaSERS fingerprinting

Identifiers

PMID40542894

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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.