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Development of a Class Prediction Model to Discriminate Pancreatic Ductal Adenocarcinoma from Pancreatic Neuroendocrine Tumor by MALDI Mass Spectrometry Imaging.

Authors :
Casadonte R
Kriegsmann M
Perren A
Baretton G
Deininger SO
Kriegsmann K
Welsch T
Pilarsky C
Kriegsmann J
Source :
Proteomics. Clinical applications [Proteomics Clin Appl] 2019 Jan; Vol. 13 (1), pp. e1800046. Date of Electronic Publication: 2018 Dec 19.
Publication Year :
2019

Abstract

Purpose: To define proteomic differences between pancreatic ductal adenocarcinoma (pDAC) and pancreatic neuroendocrine tumor (pNET) by matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI MSI).<br />Experimental Design: Ninety-three pDAC and 126 pNET individual tissues are assembled in tissue microarrays and analyzed by MALDI MSI. The cohort is separated in a training (52 pDAC and 83 pNET) and validation set (41 pDAC and 43 pNET). Subsequently, a linear discriminant analysis (LDA) model based on 46 peptide ions is performed on the training set and evaluated on the validation cohort. Additionally, two liver metastases and a whole slide of pDAC are analyzed by the same LDA algorithm.<br />Results: Classification of pDAC and pNET by the LDA model is correct in 95% (39/41) and 100% (43/43) of patients in the validation cohort, respectively. The two liver metastases and the whole slide of pDAC are also correctly classified in agreement with the histopathological diagnosis.<br />Conclusion and Clinical Relevance: In the present study, a large dataset of pDAC and pNET by MALDI MSI is investigated, a class prediction model that allowed separation of both entities with high accuracy is developed, and differential peptide peaks with potential diagnostic, prognostic, and predictive values are highlighted.<br /> (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1862-8354
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Proteomics. Clinical applications
Publication Type :
Academic Journal
Accession number :
30548962
Full Text :
https://doi.org/10.1002/prca.201800046