Evidence map›Paper›PMID 40589150›Full record

ArticleMolecular oncology2025

Machine learning for identifying liver and pancreas cancers through comprehensive serum glycopeptide spectra analysis: a case-control study.

Motoyuki Kohjima, Yuko Takami, Ken Kawabe, Kazuhiro Tanabe, Chihiro Hayashi, Mikio Mikami, Tetsuya Kusumoto

Abstract read
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Motoyuki KohjimaDepartment of Gastroenterology, NHO Kyushu Medical Center, Fukuoka, Japan.
Yuko TakamiDepartment of Hepato-Biliary-Pancreatic Surgery, NHO Kyushu Medical Center, Fukuoka, Japan.
Ken KawabeDepartment of Gastroenterology, NHO Kyushu Medical Center, Fukuoka, Japan.
Kazuhiro TanabeMedical Solution Promotion Department, Medical Solution Segment, LSI Medience Corporation, Tokyo, Japan.ORCID 0000-0003-2671-1217
Chihiro HayashiMedical Solution Promotion Department, Medical Solution Segment, LSI Medience Corporation, Tokyo, Japan.
Mikio MikamiChigasaki Central Hospital, Women's Center, Kanagawa, Japan.
Tetsuya KusumotoDepartment of Gastrointestinal Surgery and Clinical Research Institute Cancer, Research Division, NHO Kyushu Medical Center, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver and pancreatic cancers are difficult to detect early, leading to high mortality rates. Blood-based diagnostics present a viable alternative for earlier detection, potentially improving survival rates. The comprehensive serum glycopeptide spectra analysis (CSGSA) method combines enriched glycopeptides (EGPs) with conventional tumor markers through machine learning to accurately identify early stage cancers. Here, we analyzed nine tumor markers (CA19-9, AFP, PSA, CEA, CA125, CYFRA, CA15-3, SCC antigen, and NCC-ST439) in 119 patients with pancreatic cancer and 49 with hepatocellular carcinoma, alongside 590 healthy controls. We also analyzed EGPs using liquid chromatography-mass spectrometry. We found that α1-antitrypsin with a fully sialylated biantennary glycan at asparagine 271 and α2-macroglobulin with a fully sialylated biantennary glycan at asparagine 70 effectively distinguished liver and pancreatic cancers. The integration of these two glycopeptides, along with the nine tumor markers and 1688 EGPs using a machine learning model enhanced diagnostic accuracy, achieving a receiver operating characteristic-area under curve (ROC-AUC) score of 0.996. CSGSA has the potential to minimize the need for invasive diagnostic procedures and serves as a promising tool for widespread screening.

Indexed as

Biomarkers, TumorGlycopeptidesLiver NeoplasmsMachine LearningPancreatic NeoplasmsAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedROC CurveBiomarkers, TumorGlycopeptidesblood‐based diagnosticsglycopeptidesliver cancermachine learningpancreatic cancertumor markers

Identifiers

PMID40589150
PMCPMC12688161

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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.