Proteomic biomarkers predicting lymph node involvement in serum of cervical cancer patients. Limitations of SELDI-TOF MS

被引:7
|
作者
Van Gorp, Toon [1 ,2 ]
Cadron, Isabelle [1 ,3 ]
Daemen, Anneleen [1 ,4 ,5 ]
De Moor, Bart [4 ]
Waelkens, Etienne [6 ]
Vergote, Ignace [1 ]
机构
[1] Katholieke Univ Leuven, Univ Ziekenhuizen Leuven, Leuven Canc Inst, Dept Obstet & Gynaecol, B-3000 Louvain, Belgium
[2] GROW Sch Oncol & Dev Biol, MUMC, Dept Obstet & Gynaecol, NL-6229 HX Maastricht, Netherlands
[3] AZ Turnhout, Dept Obstet & Gynaecol, B-2300 Turnhout, Belgium
[4] UCSF Sch Med, Dept Lab Med, San Francisco, CA 94143 USA
[5] ESAT SCD SISTA, Dept Elect Engn, B-3001 Heverlee, Belgium
[6] Katholieke Univ Leuven, Univ Ziekenhuizen Leuven, Dept Mol Cell Biol, B-3000 Louvain, Belgium
关键词
Cervical cancer; Biomarker; Recurrence; Lymph node; SELDI-TOF MS; STAGE-IB; CARCINOMA; IIA; METASTASES; DEPLETION; PROTEINS; HISTORY;
D O I
10.1186/1477-5956-10-41
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Lymph node status is not part of the staging system for cervical cancer, but provides important information for prognosis and treatment. We investigated whether lymph node status can be predicted with proteomic profiling. Material & methods: Serum samples of 60 cervical cancer patients (FIGOI/II) were obtained before primary treatment. Samples were run through a HPLC depletion column, eliminating the 14 most abundant proteins ubiquitously present in serum. Unbound fractions were concentrated with spin filters. Fractions were spotted onto CM10 and IMAC30 surfaces and analyzed with surface-enhanced laser desorption time of flight (SELDI-TOF) mass spectrometry (MS). Unsupervised peak detection and peak clustering was performed using MASDA software. Leave-one-out (LOO) validation for weighted Least Squares Support Vector Machines (LSSVM) was used for prediction of lymph node involvement. Other outcomes were histological type, lymphvascular space involvement (LVSI) and recurrent disease. Results: LSSVM models were able to determine LN status with a LOO area under the receiver operating characteristics curve (AUC) of 0.95, based on peaks with m/z values 2,698.9, 3,953.2, and 15,254.8. Furthermore, we were able to predict LVSI (AUC 0.81), to predict recurrence (AUC 0.92), and to differentiate between squamous carcinomas and adenocarcinomas (AUC 0.88), between squamous and adenosquamous carcinomas (AUC 0.85), and between adenocarcinomas and adenosquamous carcinomas (AUC 0.94). Conclusions: Potential markers related with lymph node involvement were detected, and protein/peptide profiling support differentiation between various subtypes of cervical cancer. However, identification of the potential biomarkers was hampered by the technical limitations of SELDI-TOF MS.
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页数:8
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