MDM2 Amplified Sarcomas: A Literature Review

Murine Double Minute Clone 2, located at 12q15, is an oncogene that codes for an oncoprotein of which the association with p53 was discovered 30 years ago. The most important function of MDM2 is to control p53 activity; it is in fact the best documented negative regulator of p53. Mutations of the tu...

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Main Author: Raf Sciot
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/11/3/496
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author Raf Sciot
author_facet Raf Sciot
author_sort Raf Sciot
collection DOAJ
description Murine Double Minute Clone 2, located at 12q15, is an oncogene that codes for an oncoprotein of which the association with p53 was discovered 30 years ago. The most important function of MDM2 is to control p53 activity; it is in fact the best documented negative regulator of p53. Mutations of the tumor suppressor gene p53 represent the most frequent genetic change in human cancers. By overexpressing MDM2, cancer cells have another means to block p53. The sarcomas in which MDM2 amplification is a hallmark are well-differentiated liposarcoma/atypical lipomatous tumor, dedifferentiated liposarcoma, intimal sarcoma, and low-grade osteosarcoma. The purpose of this review is to summarize the typical clinical, histopathological, immunohistochemical, and genetic features of these tumors.
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spelling doaj.art-47e866a0551641ad8532832718942e082023-11-21T10:05:28ZengMDPI AGDiagnostics2075-44182021-03-0111349610.3390/diagnostics11030496MDM2 Amplified Sarcomas: A Literature ReviewRaf Sciot0Department of Pathology, University Hospital, University of Leuven, 3000 Leuven, BelgiumMurine Double Minute Clone 2, located at 12q15, is an oncogene that codes for an oncoprotein of which the association with p53 was discovered 30 years ago. The most important function of MDM2 is to control p53 activity; it is in fact the best documented negative regulator of p53. Mutations of the tumor suppressor gene p53 represent the most frequent genetic change in human cancers. By overexpressing MDM2, cancer cells have another means to block p53. The sarcomas in which MDM2 amplification is a hallmark are well-differentiated liposarcoma/atypical lipomatous tumor, dedifferentiated liposarcoma, intimal sarcoma, and low-grade osteosarcoma. The purpose of this review is to summarize the typical clinical, histopathological, immunohistochemical, and genetic features of these tumors.https://www.mdpi.com/2075-4418/11/3/496MDM2 amplificationwell-differentiated liposarcoma/atypical lipomatous tumordedifferentiated liposarcomaintimal sarcoma low grade osteosarcoma
spellingShingle Raf Sciot
MDM2 Amplified Sarcomas: A Literature Review
Diagnostics
MDM2 amplification
well-differentiated liposarcoma/atypical lipomatous tumor
dedifferentiated liposarcoma
intimal sarcoma low grade osteosarcoma
title MDM2 Amplified Sarcomas: A Literature Review
title_full MDM2 Amplified Sarcomas: A Literature Review
title_fullStr MDM2 Amplified Sarcomas: A Literature Review
title_full_unstemmed MDM2 Amplified Sarcomas: A Literature Review
title_short MDM2 Amplified Sarcomas: A Literature Review
title_sort mdm2 amplified sarcomas a literature review
topic MDM2 amplification
well-differentiated liposarcoma/atypical lipomatous tumor
dedifferentiated liposarcoma
intimal sarcoma low grade osteosarcoma
url https://www.mdpi.com/2075-4418/11/3/496
work_keys_str_mv AT rafsciot mdm2amplifiedsarcomasaliteraturereview