Evidence map›Paper›PMID 42403018›Full record

ArticleSmall methods2026

Machine Learning-Assisted SERS Quantification of Sialylated Alpha-Fetoprotein: From Single-Cell Analysis to Hepatocellular Carcinoma Risk Assessment.

Yu Xiao, Baolin Li, Chengyao Geng, Yuru Wang, Xiaoqian Wu, Shan Wu, Ye Zhao, Dayu Chen, Feng Yan, Jinbo Liu and 2 more

Abstract read
In one paragraph

Article in Small methods, 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

12 authors.

Yu XiaoDepartment of Medical Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Baolin LiDepartment of Medical Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, China.ORCID https://orcid.org/0000-0003-2087-172X
Chengyao GengState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.
Yuru WangState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.
Xiaoqian WuState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.
Shan WuState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.
Ye ZhaoState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.
Dayu ChenDepartment of Clinical Laboratory, Nanjing Medical University Affiliated & Cancer Hospital & Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, China.
Feng YanDepartment of Clinical Laboratory, Nanjing Medical University Affiliated & Cancer Hospital & Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, Nanjing, China.
Jinbo LiuDepartment of Medical Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yunlong ChenState Key Laboratory of Analytical Chemistry For Life Science, School of Chemistry, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0002-3775-3028
Huangxian JuDepartment of Medical Laboratory, Affiliated Hospital of Southwest Medical University, Luzhou, China.

Funding

National Natural Science Foundation of China 22474057State Key Laboratory of Analytical Chemistry for Life Science 5431ZZXM2604
6 · The paper itself

Abstract

Sialylated alpha-fetoprotein (sAFP) is a very potential marker for the pathogenesis exploration and clinical assessment of hepatocellular carcinoma (HCC). The specific and sensitive quantification of sAFP across multiple aspects is a primary premise. This work constructs a functionalized gold/silver nanocube-encapsulated microgel (Au/AgNC-MG), which can specifically capture sAFP through dual aptamer-based recognition and generate sensitive Raman fingerprints through the heterogeneous bimetallic SERS system. To further improve the specificity and quantifiability of sAFP detection in different scenarios, a series of machine learning (ML) algorithms, including a sAFP classification algorithm, a sAFP image-processing algorithm, and a sAFP-based clinical HCC risk assessment algorithm, were established for sAFP quantification, imaging of single-cell secreted sAFP, and clinical HCC risk assessment from general check-up to cirrhosis clinic patient populations. An online HCC Risk Assessment website is built for the convenience of practical clinical application. The constructed Au/AgNC-MG and established ML algorithms compose a general paradigm for HCC-related laboratory research and clinical applications.

Indexed as

alpha-FetoproteinsCarcinoma, HepatocellularLiver NeoplasmsMachine LearningSingle-Cell AnalysisSpectrum Analysis, RamanAlgorithmsClassification AlgorithmsGoldHumansMetal NanoparticlesRisk AssessmentSilveralpha-FetoproteinsGoldSilverclinical risk assessmenthepatocellular carcinomamachine learningSERSsialylated alpha‐fetoprotein

Identifiers

PMID42403018
PMCPMC13450343

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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.