Evidence map›Paper›PMID 42043839›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

A Dual-Channel Synergistic Ultrasensitive Biosensor for Tumor Liquid Biopsy.

Yu Sun, Jing Zhang, Chenqing Liu, Jing Lou, Sihui Wang, Xiangtian Ji, Xiaofang Zhao, Shirui Xu, Jingyu Feng, Bin Liu and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Yu SunDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Jing ZhangInnovation Laboratory of Terahertz Biophysics, National Innovation Institute of Defense Technology, Beijing, P. R. China.
Chenqing LiuDepartment of Otorhinolaryngology, Head and Neck Surgery, The Sixth Medical Center of the Chinese PLA General Hospital, Beijing, P. R. China.
Jing LouInnovation Laboratory of Terahertz Biophysics, National Innovation Institute of Defense Technology, Beijing, P. R. China.
Sihui WangDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Xiangtian JiDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Xiaofang ZhaoDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Shirui XuDepartment of Intensive Care Unit, Peking University Third Hospital, Beijing, P. R. China.
Jingyu FengDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Bin LiuDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.
Chao ChangInnovation Laboratory of Terahertz Biophysics, National Innovation Institute of Defense Technology, Beijing, P. R. China.
Qinggang GeDepartment of Intensive Care Unit, Peking University Third Hospital, Beijing, P. R. China.
Jun YangDepartment of Neurosurgery, Peking University Third Hospital, Beijing, P. R. China.ORCID https://orcid.org/0000-0002-7460-2800

Funding

National Natural Science Foundation of China 12225511National Natural Science Foundation of China 12304354National Natural Science Foundation of China 82072774National Natural Science Foundation of China 82272675National Natural Science Foundation of China 82501702National Natural Science Foundation of China T2241002
6 · The paper itself

Abstract

Liquid biopsy technology, which detects circulating tumor DNA (ctDNA) in cerebrospinal fluid, plays a crucial role in the early diagnosis and precision treatment of gliomas. However, the intrinsically low abundance and rapid clearance of ctDNA pose substantial challenges for conventional analytical techniques, such as droplet digital PCR and next-generation sequencing. Here, we introduce a label-free dual-channel synergistic detection strategy that enables quantitative analysis of ctDNA at the zeptomolar level. Leveraging a synergistic design that includes structural symmetry breaking and momentum condition regulation, the optical platform overcomes the inherent structural field confinement and enhances the effectiveness of target-contacted sensing. By integrating a DNA tetrahedron-hybridization chain reaction-gold nanoparticle cascade amplification system, the dual-channel synergistic biosensor achieves an ultra-low detection limit of 74 zM while covering a dynamic range spanning 12 orders of magnitude. Clinical validation has confirmed that this dual-channel synergistic detection strategy can accurately identify the IDH1.R132H mutation in glioma patients with as little as 1 µL of sample, and deliver crucial clinical information such as tumor size and staging. This label-free, rapid, cost-effective, and highly sensitive biosensing platform offers a powerful tool for early cancer screening, molecular diagnostics, and longitudinal disease monitoring.

Indexed as

Biosensing TechniquesBrain NeoplasmsCirculating Tumor DNAGliomaBiomarkers, TumorGoldHumansIsocitrate DehydrogenaseLiquid BiopsyMetal NanoparticlesBiomarkers, TumorCirculating Tumor DNAGoldIsocitrate DehydrogenaseGliomaIDH1Liquid BiopsyMetasurfaceQBIC

Identifiers

PMID42043839
PMCPMC13335429

What OpenQuestion holds

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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.