Evidence map›Paper›PMID 41188770›Full record

ArticleBMC cancer2025

Plasma lipidomics for biomarker identification in non-muscle invasive bladder cancer.

Yi Zhao, Zhigang Ji, Wei Sun, Xiaoyan Liu

Abstract read
In one paragraph

Article in BMC cancer, 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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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

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0 citing papers in PubMed.

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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

4 authors.

Yi ZhaoDepartment of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Zhigang JiDepartment of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China. jzg_pumch@163.com.
Wei SunInstitute of Basic Medical Sciences, School of Basic Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Xiaoyan LiuInstitute of Basic Medical Sciences, School of Basic Medicine, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBladder cancer is a high-incidence malignant tumor in the world. Currently available potential biomarkers lack sufficient diagnostic accuracy, underscoring the need for novel biomarkers. Lipid metabolites have emerged as promising candidates for diagnosing malignant tumors in recent years. Few studies explored the potential value of lipids in bladder cancer. Our study investigated plasma lipid metabolism markers in non-muscle invasive bladder cancer (NMIBC) using liquid chromatography-high resolution mass spectrometry (LC-HRMS).

methodsOverall, 214 cases were included, with 106 NMIBC patients as NMIBC group and 108 healthy adults as control group. Plasma lipids were profiled using LC-HRMS to distinguish NMIBC group from control group, low-grade NMIBC group from control group and low-grade NMIBC group from high-grade NMIBC group.

resultsApparent separation was observed between NMIBC group and control group. Hydroxy fatty acids, O-TAG, O-LPG and hydrocarbons metabolites were significantly enriched in NMIBC group. A Lipids panel of PE(14:1/20:0), PE(18:2/16:0) and 19-methyl-heneicosanoic acid was used to conduct a predictive model of NMIBC group and control group. The model showed acceptable accuracy for NMIBC diagnosis with the area under the curve (AUC) of 0.88 and 0,82 for training and validation cohorts, respectively, especially for the low-grade NMIBC diagnosis with the AUC of 0.81. For low- and high-grade NMIBC distinction, a panel of four lipids achieved good performance with the AUC value of 0.815 (10-fold cross validation: 0.77; leave-one-out validation (LOOCV):0.77).

conclusionLipid profiles differed significantly between patients with non-muscle invasive bladder cancer (NMIBC) and healthy adults. The identified lipid biomarkers demonstrated high discriminatory accuracy in diagnosing and grading NMIBC, indicating their promising clinical potential for both detection and monitoring of bladder cancer.

Indexed as

Biomarkers, TumorLipidomicsLipidsUrinary Bladder NeoplasmsAdultAgedAged, 80 and overCase-Control StudiesChromatography, LiquidFemaleHumansLipid MetabolismMaleMass SpectrometryMiddle AgedNeoplasm InvasivenessBiomarkers, TumorLipidsBiomarkersDiagnosisLC-HRMSLipidomicsNMIBC

Identifiers

PMID41188770
PMCPMC12584469

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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.