Evidence map›Paper›PMID 42496706›Full record

ArticleAnalytical and bioanalytical chemistry2026

A systematic DoE approach for optimizing urinary LC-HRMS metabolomics: enhancing reliability in bladder cancer profiling.

Anastasiia Frolova, Mikhail Vokuev, Yurii Ikhalainen, Daria Prosuntsova, Igor Rodin

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Article in Analytical and bioanalytical chemistry, 2026. 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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5 · Who and what money

Authors and funding

5 authors.

Anastasiia FrolovaDepartment of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russia. avolorf.msu@gmail.com.
Mikhail VokuevDepartment of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russia.
Yurii IkhalainenDepartment of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russia.
Daria ProsuntsovaDepartment of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russia.
Igor RodinDepartment of Chemistry, Lomonosov Moscow State University, 119991, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Untargeted urinary metabolomics presents significant challenges in analytical reproducibility and biological interpretation, particularly in the context of clinical oncology. This study presents a systematically optimized liquid chromatography-high-resolution mass spectrometry (LC-HRMS) workflow for bladder cancer (BCa) biomarker discovery. To address variability in sample preparation, a two-stage design of experiments (DoE) approach was applied to systematically optimize key parameters affecting metabolite extraction efficiency, thereby improving the reproducibility of subsequent non-invasive profiling. The performance of the workflow was evaluated through the systematic assessment of instrumental stability and injection precision using pooled quality control (QC) samples. Following peak picking and alignment, a comprehensive raw dataset of 15,344 metabolic signals was generated, leading to the putative identification of 854 compounds. Unsupervised principal component analysis (PCA) demonstrated reproducible instrumental performance, indicated by tight QC sample clustering. From the total clinical cohort of 107 patients, a demographically matched sub-cohort of 50 individuals was evaluated to suppress confounding physiological noise. This comparative model revealed distinct disease-specific clustering and demonstrated significant perturbations in the tryptophan metabolic axis, membrane lipid remodeling, and enhanced proteolytic activity, characterized by an evident peptide overflow, associated with BCa progression. This systematically optimized methodology provides a reliable analytical approach for identifying non-invasive diagnostic panels, supporting the implementation of efficient laboratory workflows aligned with Analytics 5.0 principles.

Indexed as

Biomarkers, TumorLiquid Chromatography-Mass SpectrometryMetabolomicsUrinary Bladder NeoplasmsChromatography, LiquidHumansPrincipal Component AnalysisReproducibility of ResultsBiomarkers, TumorAnalytics 5.0Bladder cancer biomarkersDesign of experiments (DoE)LC-HRMSUntargeted metabolomics

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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.