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FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations

MDM2 amplification represents the leading oncogenic pathway and diagnostic hallmark of liposarcoma, whose assessment is based on Fluorescence In Situ Hybridization (FISH) analysis. Despite its diagnostic relevance, no univocal interpretation criteria regarding FISH assessments of MDM2 amplification...

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Autores principales: Gambella, Alessandro, Bertero, Luca, Rondón-Lagos, Milena, Verdun Di Cantogno, Ludovica, Rangel, Nelson, Pitino, Chiara, Ricci, Alessia Andrea, Mangherini, Luca, Castellano, Isabella, Cassoni, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863600/
https://www.ncbi.nlm.nih.gov/pubmed/36674856
http://dx.doi.org/10.3390/ijms24021342
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author Gambella, Alessandro
Bertero, Luca
Rondón-Lagos, Milena
Verdun Di Cantogno, Ludovica
Rangel, Nelson
Pitino, Chiara
Ricci, Alessia Andrea
Mangherini, Luca
Castellano, Isabella
Cassoni, Paola
author_facet Gambella, Alessandro
Bertero, Luca
Rondón-Lagos, Milena
Verdun Di Cantogno, Ludovica
Rangel, Nelson
Pitino, Chiara
Ricci, Alessia Andrea
Mangherini, Luca
Castellano, Isabella
Cassoni, Paola
author_sort Gambella, Alessandro
collection PubMed
description MDM2 amplification represents the leading oncogenic pathway and diagnostic hallmark of liposarcoma, whose assessment is based on Fluorescence In Situ Hybridization (FISH) analysis. Despite its diagnostic relevance, no univocal interpretation criteria regarding FISH assessments of MDM2 amplification have been established so far, leading to several different approaches and potential diagnostic misinterpretations. This study aims to address the most common issues and proposes troubleshooting guidelines for MDM2 amplification assessments by FISH. We retrospectively retrieved 51 liposarcomas, 25 Lipomas, 5 Spindle Cell Lipoma/Pleomorphic Lipomas, and 2 Atypical Spindle Cell Lipomatous Tumors and the corresponding MDM2 FISH analysis. We observed MDM2 amplification in liposarcomas cases only (43 out of 51 cases) and identified three MDM2-amplified patterns (scattered (50% of cases), clustered (14% of cases), and mixed (36% of cases)) and two nonamplified patterns (low number of signals (82% of cases) and polysomic (18% of cases)). Based on these data and published evidence in the literature, we propose a set of criteria to guide MDM2 amplification analysis in liposarcoma. Kindled by the compelling importance of MDM2 assessments to improve diagnostic and therapeutic liposarcoma management, these suggestions could represent the first step to develop a univocal interpretation model and consensus guidelines.
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spelling pubmed-98636002023-01-22 FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations Gambella, Alessandro Bertero, Luca Rondón-Lagos, Milena Verdun Di Cantogno, Ludovica Rangel, Nelson Pitino, Chiara Ricci, Alessia Andrea Mangherini, Luca Castellano, Isabella Cassoni, Paola Int J Mol Sci Article MDM2 amplification represents the leading oncogenic pathway and diagnostic hallmark of liposarcoma, whose assessment is based on Fluorescence In Situ Hybridization (FISH) analysis. Despite its diagnostic relevance, no univocal interpretation criteria regarding FISH assessments of MDM2 amplification have been established so far, leading to several different approaches and potential diagnostic misinterpretations. This study aims to address the most common issues and proposes troubleshooting guidelines for MDM2 amplification assessments by FISH. We retrospectively retrieved 51 liposarcomas, 25 Lipomas, 5 Spindle Cell Lipoma/Pleomorphic Lipomas, and 2 Atypical Spindle Cell Lipomatous Tumors and the corresponding MDM2 FISH analysis. We observed MDM2 amplification in liposarcomas cases only (43 out of 51 cases) and identified three MDM2-amplified patterns (scattered (50% of cases), clustered (14% of cases), and mixed (36% of cases)) and two nonamplified patterns (low number of signals (82% of cases) and polysomic (18% of cases)). Based on these data and published evidence in the literature, we propose a set of criteria to guide MDM2 amplification analysis in liposarcoma. Kindled by the compelling importance of MDM2 assessments to improve diagnostic and therapeutic liposarcoma management, these suggestions could represent the first step to develop a univocal interpretation model and consensus guidelines. MDPI 2023-01-10 /pmc/articles/PMC9863600/ /pubmed/36674856 http://dx.doi.org/10.3390/ijms24021342 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gambella, Alessandro
Bertero, Luca
Rondón-Lagos, Milena
Verdun Di Cantogno, Ludovica
Rangel, Nelson
Pitino, Chiara
Ricci, Alessia Andrea
Mangherini, Luca
Castellano, Isabella
Cassoni, Paola
FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title_full FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title_fullStr FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title_full_unstemmed FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title_short FISH Diagnostic Assessment of MDM2 Amplification in Liposarcoma: Potential Pitfalls and Troubleshooting Recommendations
title_sort fish diagnostic assessment of mdm2 amplification in liposarcoma: potential pitfalls and troubleshooting recommendations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9863600/
https://www.ncbi.nlm.nih.gov/pubmed/36674856
http://dx.doi.org/10.3390/ijms24021342
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