Evidence map›Paper›PMID 41284888›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Lipidomic profiling of endometrial cancer using desorption electrospray ionization mass spectrometry imaging.

Maria Paraskevaidi, Olivia Raglan, James McKenzie, Yuchen Xiang, Stefania Maneta-Stavrakaki, Maria Luisa Doria, Apostolia Galani, Nada Assi, Eftychios Manoli, Laura Burney Ellis and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Lipidomic profiling of endometrial cancer using desorption electrospray ionization mass spectrometry imaging.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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.

Maria ParaskevaidiDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-1353-7849
Olivia RaglanWest London Gynaecological Cancer Centre, Imperial College Healthcare National Health Service Trust, London W12 0HS, United Kingdom.
James McKenzieDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Yuchen XiangDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Stefania Maneta-StavrakakiDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Maria Luisa DoriaDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Apostolia GalaniDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-5731-4532
Nada AssiBiostatistics Department, HEVA, Lyon 69006, France.
Eftychios ManoliDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Laura Burney EllisDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Baljeet KaurImperial College Healthcare National Health Service Trust, North West London Pathology, London W12 0HS, United Kingdom.
Francesca RosiniImperial College Healthcare National Health Service Trust, North West London Pathology, London W12 0HS, United Kingdom.
Marc J GunterSchool of Public Health, Faculty of Medicine, Imperial College London, London W12 0BZ, United Kingdom.
Zoltan TakatsDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.
Maria KyrgiouDepartment of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London W12 0NN, United Kingdom.ORCID 0000-0002-7165-0735

Funding

Genesis Research Trust P55549Imperial College Healthcare Charity P47907Imperial College Healthcare Charity RF16\10001Imperial Healthcare NHS Trust NIHR BRC P45272MRC Imperial Confidence in Concept PS2857MRC Imperial Confidence in Concept PS2897National Research Development and Innovation Office of Hungary KNN121510National Research Development and Innovation Office of Hungary NVKP_16-1-2016-0042Waters Corporation (Waters) P53626_WSSB
6 · The paper itself

Abstract

Novel technologies are required to improve endometrial cancer diagnosis and enhance the early detection of preinvasive precursors. Herein, desorption electrospray ionization mass spectrometry imaging (DESI-MSI) was used to differentiate malignant from benign endometrial tissues and assess lipidomic differences among patients with obesity and diabetes. Reverse phase protein array (RPPA) analysis was performed in the same patients to gain insights into the altered signaling pathways and investigate the protein expression levels in endometrial cancer cases and controls. Tissues from 64 women (50 cancer, 14 benign) were analyzed with DESI-MSI achieving 90% sensitivity and 93% specificity. Discriminatory spectral features were primarily phospholipids [phosphatidic acid (PA), phosphatidylethanolamine (PE), phosphatidylserine (PS), and phosphatidylinositol (PI)], all elevated in cancer. Proteomics revealed upregulated proteins linked to commonly dysregulated pathways in endometrial cancer, namely PI3K/AKT/mTOR, MAPK/RAS, and Wnt signaling pathways. Lipidomic differences were found between high- (obesity/diabetes) and low-risk phenotypes (no obesity/diabetes), with PE and PS elevated in high-risk benign and PE reduced in high-risk cancer cases. A single phospholipid (PE(O-38:4)) was found as discriminatory in both normal and cancer cohorts, which may serve as biomarker in women with benign histology at high-risk of developing endometrial cancer. This study reports the application of DESI-MSI for lipidomic characterisation of endometrial cancer.

Indexed as

Endometrial NeoplasmsLipidomicsSpectrometry, Mass, Electrospray IonizationAdultAgedFemaleHumansMiddle AgedObesityProteomicsSignal Transductiondesorption electrospray ionization mass spectrometry imaging (DESI-MSI)endometrial cancerlipidomicsproteomics

Identifiers

PMID41284888
PMCPMC12685106

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.