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Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?

SIMPLE SUMMARY: Myxofibrosarcoma (MFS) is one of the most common malignant soft tissue sarcomas. MFS occurs mostly in the extremities of patients after the fifth decade of life as a painless a slow-growing mass. In most of the cases treatment is surgical resection of the tumor. However, at times sur...

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Autores principales: Lucarelli, Enrico, De Vita, Alessandro, Bellotti, Chiara, Frisoni, Tommaso, Vanni, Silvia, Guerrieri, Ania Naila, Pannella, Micaela, Mercatali, Laura, Gambarotti, Marco, Duchi, Serena, Miserocchi, Giacomo, Maioli, Margherita, Liverani, Chiara, Ibrahim, Toni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650645/
https://www.ncbi.nlm.nih.gov/pubmed/37958307
http://dx.doi.org/10.3390/cancers15215132
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author Lucarelli, Enrico
De Vita, Alessandro
Bellotti, Chiara
Frisoni, Tommaso
Vanni, Silvia
Guerrieri, Ania Naila
Pannella, Micaela
Mercatali, Laura
Gambarotti, Marco
Duchi, Serena
Miserocchi, Giacomo
Maioli, Margherita
Liverani, Chiara
Ibrahim, Toni
author_facet Lucarelli, Enrico
De Vita, Alessandro
Bellotti, Chiara
Frisoni, Tommaso
Vanni, Silvia
Guerrieri, Ania Naila
Pannella, Micaela
Mercatali, Laura
Gambarotti, Marco
Duchi, Serena
Miserocchi, Giacomo
Maioli, Margherita
Liverani, Chiara
Ibrahim, Toni
author_sort Lucarelli, Enrico
collection PubMed
description SIMPLE SUMMARY: Myxofibrosarcoma (MFS) is one of the most common malignant soft tissue sarcomas. MFS occurs mostly in the extremities of patients after the fifth decade of life as a painless a slow-growing mass. In most of the cases treatment is surgical resection of the tumor. However, at times surgeons can’t distinguish the boundaries of the tumor and are unable to remove all the tumor cells. Therefore, the tumor cells left in the patients can spread and grow again (recurrence). When MFS recurs more than once it is a challenge for clinicians and a burden for patients. Therefore, especially for patients that recur more than once new therapeutic approaches are needed. In vitro and in vivo models are helpful to understand the disease and to test new therapeutic agents. This review details the available MFS models, identifies critical issues of each model, and suggests models that would be useful to develop in the future. ABSTRACT: Myxofibrosarcoma (MFS) is a malignant soft tissue sarcoma (STS) that originates in the body’s connective tissues. It is characterized by the presence of myxoid (gel-like) and fibrous components and typically affects patients after the fifth decade of life. Considering the ongoing trend of increasing lifespans across many nations, MFS is likely to become the most common musculoskeletal sarcoma in the future. Although MFS patients have a lower risk of developing distant metastases compared with other STS cases, MFS is characterized by a high frequency of local recurrence. Notably, in 40–60% of the patients where the tumor recurs, it does so multiple times. Consequently, patients may undergo multiple local surgeries, removing the risk of potential amputation. Furthermore, because the tumor relapses generally have a higher grade, they exhibit a decreased response to radio and chemotherapy and an increased tendency to form metastases. Thus, a better understanding of MFS is required, and improved therapeutic options must be developed. Historically, preclinical models for other types of tumors have been instrumental in obtaining a better understanding of tumor development and in testing new therapeutic approaches. However, few MFS models are currently available. In this review, we will describe the MFS models available and will provide insights into the advantages and constraints of each model.
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spelling pubmed-106506452023-10-25 Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing? Lucarelli, Enrico De Vita, Alessandro Bellotti, Chiara Frisoni, Tommaso Vanni, Silvia Guerrieri, Ania Naila Pannella, Micaela Mercatali, Laura Gambarotti, Marco Duchi, Serena Miserocchi, Giacomo Maioli, Margherita Liverani, Chiara Ibrahim, Toni Cancers (Basel) Review SIMPLE SUMMARY: Myxofibrosarcoma (MFS) is one of the most common malignant soft tissue sarcomas. MFS occurs mostly in the extremities of patients after the fifth decade of life as a painless a slow-growing mass. In most of the cases treatment is surgical resection of the tumor. However, at times surgeons can’t distinguish the boundaries of the tumor and are unable to remove all the tumor cells. Therefore, the tumor cells left in the patients can spread and grow again (recurrence). When MFS recurs more than once it is a challenge for clinicians and a burden for patients. Therefore, especially for patients that recur more than once new therapeutic approaches are needed. In vitro and in vivo models are helpful to understand the disease and to test new therapeutic agents. This review details the available MFS models, identifies critical issues of each model, and suggests models that would be useful to develop in the future. ABSTRACT: Myxofibrosarcoma (MFS) is a malignant soft tissue sarcoma (STS) that originates in the body’s connective tissues. It is characterized by the presence of myxoid (gel-like) and fibrous components and typically affects patients after the fifth decade of life. Considering the ongoing trend of increasing lifespans across many nations, MFS is likely to become the most common musculoskeletal sarcoma in the future. Although MFS patients have a lower risk of developing distant metastases compared with other STS cases, MFS is characterized by a high frequency of local recurrence. Notably, in 40–60% of the patients where the tumor recurs, it does so multiple times. Consequently, patients may undergo multiple local surgeries, removing the risk of potential amputation. Furthermore, because the tumor relapses generally have a higher grade, they exhibit a decreased response to radio and chemotherapy and an increased tendency to form metastases. Thus, a better understanding of MFS is required, and improved therapeutic options must be developed. Historically, preclinical models for other types of tumors have been instrumental in obtaining a better understanding of tumor development and in testing new therapeutic approaches. However, few MFS models are currently available. In this review, we will describe the MFS models available and will provide insights into the advantages and constraints of each model. MDPI 2023-10-25 /pmc/articles/PMC10650645/ /pubmed/37958307 http://dx.doi.org/10.3390/cancers15215132 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 Review
Lucarelli, Enrico
De Vita, Alessandro
Bellotti, Chiara
Frisoni, Tommaso
Vanni, Silvia
Guerrieri, Ania Naila
Pannella, Micaela
Mercatali, Laura
Gambarotti, Marco
Duchi, Serena
Miserocchi, Giacomo
Maioli, Margherita
Liverani, Chiara
Ibrahim, Toni
Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title_full Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title_fullStr Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title_full_unstemmed Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title_short Modeling Myxofibrosarcoma: Where Do We Stand and What Is Missing?
title_sort modeling myxofibrosarcoma: where do we stand and what is missing?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650645/
https://www.ncbi.nlm.nih.gov/pubmed/37958307
http://dx.doi.org/10.3390/cancers15215132
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