Evidence map›Paper›PMID 38194998›Full record

ArticleMolecular oncology2024

Single extracellular vesicle surface protein-based blood assay identifies potential biomarkers for detection and screening of five cancers.

Yuxin Min, Wenjiang Deng, Huangbo Yuan, Dongliang Zhu, Renjia Zhao, Pengyan Zhang, Jiangli Xue, Ziyu Yuan, Tiejun Zhang, Yanfeng Jiang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Effect of Extracellular Vesicles Derived From Tumor Cells on Immune Evasion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

15 authors at 4 institutions in 2 countries.

Yuxin MinDepartment of Epidemiology, School of Public Health, Fudan University, Shanghai, China.
Wenjiang DengDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
Huangbo YuanState Key Laboratory of Genetic Engineering, School of Life Science, Human Phenome Institute, Fudan University, Shanghai, China.
Dongliang ZhuDepartment of Epidemiology, School of Public Health, Fudan University, Shanghai, China.
Renjia ZhaoState Key Laboratory of Genetic Engineering, School of Life Science, Human Phenome Institute, Fudan University, Shanghai, China.
Pengyan ZhangDepartment of Epidemiology, School of Public Health, Fudan University, Shanghai, China.
Jiangli XueFudan University Taizhou Institute of Health Sciences, Taizhou, China.
Ziyu YuanFudan University Taizhou Institute of Health Sciences, Taizhou, China.
Tiejun ZhangDepartment of Epidemiology, School of Public Health, Fudan University, Shanghai, China.
Yanfeng JiangState Key Laboratory of Genetic Engineering, School of Life Science, Human Phenome Institute, Fudan University, Shanghai, China.
Kelin XuDepartment of Biostatistics, School of Public Health, Fudan University, Shanghai, China.
Di WuVesicode AB, Stockholm, Sweden.
Yanling CaiGuangdong Provincial Key Laboratory of Systems Biology and Synthetic Biology for Urogenital Tumors, Shenzhen Key Laboratory of Genitourinary Tumor, Department of Urology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen Institute of Translational Medicine, Shenzhen, China.ORCID 0000-0002-9149-2738
Chen SuoDepartment of Epidemiology, School of Public Health, Fudan University, Shanghai, China.ORCID 0000-0002-5274-4584
Xingdong ChenFudan University Taizhou Institute of Health Sciences, Taizhou, China.ORCID 0000-0003-3763-160X
Fudan University · CNKarolinska Institutet · SEShenzhen Second People's Hospital · CNVeolia (Sweden) · SE

Funding

Innovation Grant from Science and Technology Commission of Shanghai Municipality 20ZR1405600National Key Research and Development Program of China 2017YFC0907000National Key Research and Development Program of China 2019YFC1315804National Key Research and Development Program of China 2022YFC3400700National Natural Science Foundation of China 82073637National Natural Science Foundation of China 82122060National Natural Science Foundation of China 91846302National Science & Technology Fundamental Resources Investigation Program of China 2019FY101103Shanghai Municipal Science and Technology Major Project ZD2021CY001Three-Year Action Plan for Strengthening Public Health System in Shanghai GWV-10.2-YQ32
6 · The paper itself

Abstract

Extracellular vesicles (EVs) and EV proteins are promising biomarkers for cancer liquid biopsy. Herein, we designed a case-control study involving 100 controls and 100 patients with esophageal, stomach, colorectal, liver, or lung cancer to identify common and type-specific biomarkers of plasma-derived EV surface proteins for the five cancers. EV surface proteins were profiled using a sequencing-based proximity barcoding assay. In this study, five differentially expressed proteins (DEPs) and eight differentially expressed protein combinations (DEPCs) showed promising performance (area under curve, AUC > 0.900) in pan-cancer identification [e.g., TENM2 (AUC = 0.982), CD36 (AUC = 0.974), and CD36-ITGA1 (AUC = 0.971)]. Our classification model could properly discriminate between cancer patients and controls using DEPs (AUC = 0.981) or DEPCs (AUC = 0.965). When distinguishing one cancer from the other four, the accuracy of the classification model using DEPCs (85-92%) was higher than that using DEPs (78-84%). We validated the performance in an additional 14 cancer patients and 14 controls, and achieved an AUC value of 0.786 for DEPs and 0.622 for DEPCs, highlighting the necessity to recruit a larger cohort for further validation. When clustering EVs into subpopulations, we detected cluster-specific proteins highly expressed in immune-related tissues. In the context of colorectal cancer, we identified heterogeneous EV clusters enriched in cancer patients, correlating with tumor initiation and progression. These findings provide epidemiological and molecular evidence for the clinical application of EV proteins in cancer prediction, while also illuminating their functional roles in cancer physiopathology.

Indexed as

Extracellular VesiclesLung NeoplasmsBiomarkersBiomarkers, TumorCase-Control StudiesEarly Detection of CancerHumansMembrane ProteinsBiomarkersBiomarkers, TumorMembrane ProteinsbiomarkersEV subpopulationsextracellular vesicle proteinspan-cancer

Identifiers

PMID38194998
PMCPMC10920081
OpenAlexW4390706139

What OpenQuestion holds

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LicenceCC BY
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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.