Background/Objectives: Mast cell tumors (MCTs) are the second most common malignant neoplasms in dogs. Histopathological grading and clinical staging are the main tools for estimating biological behavior and disease extent; thus, both are essential for therapeutic decision-making and prognostication. However, the biological behavior of MCTs in dogs is variable, and it sometimes deviates from expectations. In a previous study, we identified 12 transcripts whose expression profile allowed a clear distinction between Kiupel low-grade and high-grade cutaneous MCTs (cMCTs) and was associated with prognosis. Building on these findings, this study evaluated the predictive potential of these transcripts’ expression profiles in classifying cMCTs into low-grade and high- grade. Methods: A logistic regression classifier based on the expression profiles of the identified transcripts and able to classify cMCTs as low- or high-grade was developed and subsequently tested on a novel dataset of 50 cMCTs whose expression profiles have been determined in this study through qPCR. Results: The developed logistic regression classifier reaches an accuracy of 67% and an area under the receiver operating characteristic curve (AUC) of 0.76. Interestingly, the molecular classification clearly identifies stage-IV disease (90% true positive rate). Conclusions: qPCR analysis of these biomarkers combined with the machine learning-based classifier might serve as a tool to support cMCT clinical management at diagnosis.

Expression profile of twelve transcripts as a supporting tool for the molecular characterization of canine cutaneous mast cell tumors at diagnosis: association with histological grading and clinical staging / M. Giantin, L. Montanucci, R.M. Lopparelli, R. Tolosi, A. Dentini, V. Grieco, D. Stefanello, S. Sabattini, L. Marconato, M. Pauletto, M. Dacasto. - In: GENES. - ISSN 2073-4425. - 16:3(2025 Mar 14), pp. 340.1-340.15. [10.3390/genes16030340]

Expression profile of twelve transcripts as a supporting tool for the molecular characterization of canine cutaneous mast cell tumors at diagnosis: association with histological grading and clinical staging

V. Grieco
Writing – Review & Editing
;
D. Stefanello
Writing – Review & Editing
;
2025

Abstract

Background/Objectives: Mast cell tumors (MCTs) are the second most common malignant neoplasms in dogs. Histopathological grading and clinical staging are the main tools for estimating biological behavior and disease extent; thus, both are essential for therapeutic decision-making and prognostication. However, the biological behavior of MCTs in dogs is variable, and it sometimes deviates from expectations. In a previous study, we identified 12 transcripts whose expression profile allowed a clear distinction between Kiupel low-grade and high-grade cutaneous MCTs (cMCTs) and was associated with prognosis. Building on these findings, this study evaluated the predictive potential of these transcripts’ expression profiles in classifying cMCTs into low-grade and high- grade. Methods: A logistic regression classifier based on the expression profiles of the identified transcripts and able to classify cMCTs as low- or high-grade was developed and subsequently tested on a novel dataset of 50 cMCTs whose expression profiles have been determined in this study through qPCR. Results: The developed logistic regression classifier reaches an accuracy of 67% and an area under the receiver operating characteristic curve (AUC) of 0.76. Interestingly, the molecular classification clearly identifies stage-IV disease (90% true positive rate). Conclusions: qPCR analysis of these biomarkers combined with the machine learning-based classifier might serve as a tool to support cMCT clinical management at diagnosis.
canine mast cell tumor; dog; biomarker; qPCR; principal component analysis; logistic regression
Settore MVET-04/B - Clinica medica veterinaria
Settore MVET-05/A - Clinica chirurgica veterinaria
Settore MVET-02/A - Patologia generale e anatomia patologica veterinaria
14-mar-2025
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1171718
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