Quantitative SWATH-based proteomic profiling of urine for the identification of endometrial cancer biomarkers in symptomatic women

被引:11
作者
Njoku, Kelechi [1 ,2 ,3 ]
Pierce, Andrew [1 ,2 ,4 ]
Geary, Bethany [1 ,2 ]
Campbell, Amy E. [1 ,2 ]
Kelsall, Janet [2 ]
Reed, Rachel [2 ]
Armit, Alexander [2 ]
Da Sylva, Rachel [2 ]
Zhang, Liqun [1 ]
Agnew, Heather [1 ,3 ]
Baricevic-Jones, Ivona [2 ]
Chiasserini, Davide [2 ,5 ]
Whetton, Anthony D. [6 ]
Crosbie, Emma J. [1 ,2 ,3 ]
机构
[1] Univ Manchester, St Marys Hosp, Fac Biol Med & Hlth, Sch Med Sci, 5th Floor Res,Oxford Rd, Manchester M13 9WL, England
[2] Univ Manchester, Inst Canc Sci, Fac Biol Med & Hlth, Stoller Biomarker Discovery Ctr, Manchester, England
[3] Manchester Univ NHS Fdn Trust, Manchester Acad Hlth Sci Ctr, Dept Obstet & Gynaecol, Manchester, England
[4] Bangor Univ, Coll Human Sci, Sch Med & Hlth Sci, Bangor LL57 2TH, Wales, England
[5] Univ Perugia, Dept Med & Surg, Sect Physiol & Biochem, I-06132 Perugia, Italy
[6] Univ Surrey, Fac Hlth & Med Sci, Sch Vet Med, Guildford GU2 7XH, England
关键词
EXPRESSION; PROTEINS; OVARIAN; METALLOPROTEINASES;
D O I
10.1038/s41416-022-02139-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundA non-invasive endometrial cancer detection tool that can accurately triage symptomatic women for definitive testing would improve patient care. Urine is an attractive biofluid for cancer detection due to its simplicity and ease of collection. The aim of this study was to identify urine-based proteomic signatures that can discriminate endometrial cancer patients from symptomatic controls.MethodsThis was a prospective case-control study of symptomatic post-menopausal women (50 cancers, 54 controls). Voided self-collected urine samples were processed for mass spectrometry and run using sequential window acquisition of all theoretical mass spectra (SWATH-MS). Machine learning techniques were used to identify important discriminatory proteins, which were subsequently combined in multi-marker panels using logistic regression.ResultsThe top discriminatory proteins individually showed moderate accuracy (AUC > 0.70) for endometrial cancer detection. However, algorithms combining the most discriminatory proteins performed well with AUCs > 0.90. The best performing diagnostic model was a 10-marker panel combining SPRR1B, CRNN, CALML3, TXN, FABP5, C1RL, MMP9, ECM1, S100A7 and CFI and predicted endometrial cancer with an AUC of 0.92 (0.96-0.97). Urine-based protein signatures showed good accuracy for the detection of early-stage cancers (AUC 0.92 (0.86-0.9)).ConclusionA patient-friendly, urine-based test could offer a non-invasive endometrial cancer detection tool in symptomatic women. Validation in a larger independent cohort is warranted.
引用
收藏
页码:1723 / 1732
页数:10
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