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Quantitative proteomic studies addressing unmet clinical needs in sarcoma
Sarcoma is a rare and complex disease comprising over 80 malignant subtypes that is frequently characterized by poor prognosis. Challenges in clinical management include uncertainties in diagnosis and disease classification, limited prognostic and predictive biomarkers, incompletely understood disea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183589/ https://www.ncbi.nlm.nih.gov/pubmed/37197427 http://dx.doi.org/10.3389/fonc.2023.1126736 |
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author | Connolly, Elizabeth A. Grimison, Peter S. Horvath, Lisa G. Robinson, Phillip J. Reddel, Roger R. |
author_facet | Connolly, Elizabeth A. Grimison, Peter S. Horvath, Lisa G. Robinson, Phillip J. Reddel, Roger R. |
author_sort | Connolly, Elizabeth A. |
collection | PubMed |
description | Sarcoma is a rare and complex disease comprising over 80 malignant subtypes that is frequently characterized by poor prognosis. Challenges in clinical management include uncertainties in diagnosis and disease classification, limited prognostic and predictive biomarkers, incompletely understood disease heterogeneity among and within subtypes, lack of effective treatment options, and limited progress in identifying new drug targets and novel therapeutics. Proteomics refers to the study of the entire complement of proteins expressed in specific cells or tissues. Advances in proteomics have included the development of quantitative mass spectrometry (MS)-based technologies which enable analysis of large numbers of proteins with relatively high throughput, enabling proteomics to be studied on a scale that has not previously been possible. Cellular function is determined by the levels of various proteins and their interactions, so proteomics offers the possibility of new insights into cancer biology. Sarcoma proteomics therefore has the potential to address some of the key current challenges described above, but it is still in its infancy. This review covers key quantitative proteomic sarcoma studies with findings that pertain to clinical utility. Proteomic methodologies that have been applied to human sarcoma research are briefly described, including recent advances in MS-based proteomic technology. We highlight studies that illustrate how proteomics may aid diagnosis and improve disease classification by distinguishing sarcoma histologies and identify distinct profiles within histological subtypes which may aid understanding of disease heterogeneity. We also review studies where proteomics has been applied to identify prognostic, predictive and therapeutic biomarkers. These studies traverse a range of histological subtypes including chordoma, Ewing sarcoma, gastrointestinal stromal tumors, leiomyosarcoma, liposarcoma, malignant peripheral nerve sheath tumors, myxofibrosarcoma, rhabdomyosarcoma, synovial sarcoma, osteosarcoma, and undifferentiated pleomorphic sarcoma. Critical questions and unmet needs in sarcoma which can potentially be addressed with proteomics are outlined. |
format | Online Article Text |
id | pubmed-10183589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101835892023-05-16 Quantitative proteomic studies addressing unmet clinical needs in sarcoma Connolly, Elizabeth A. Grimison, Peter S. Horvath, Lisa G. Robinson, Phillip J. Reddel, Roger R. Front Oncol Oncology Sarcoma is a rare and complex disease comprising over 80 malignant subtypes that is frequently characterized by poor prognosis. Challenges in clinical management include uncertainties in diagnosis and disease classification, limited prognostic and predictive biomarkers, incompletely understood disease heterogeneity among and within subtypes, lack of effective treatment options, and limited progress in identifying new drug targets and novel therapeutics. Proteomics refers to the study of the entire complement of proteins expressed in specific cells or tissues. Advances in proteomics have included the development of quantitative mass spectrometry (MS)-based technologies which enable analysis of large numbers of proteins with relatively high throughput, enabling proteomics to be studied on a scale that has not previously been possible. Cellular function is determined by the levels of various proteins and their interactions, so proteomics offers the possibility of new insights into cancer biology. Sarcoma proteomics therefore has the potential to address some of the key current challenges described above, but it is still in its infancy. This review covers key quantitative proteomic sarcoma studies with findings that pertain to clinical utility. Proteomic methodologies that have been applied to human sarcoma research are briefly described, including recent advances in MS-based proteomic technology. We highlight studies that illustrate how proteomics may aid diagnosis and improve disease classification by distinguishing sarcoma histologies and identify distinct profiles within histological subtypes which may aid understanding of disease heterogeneity. We also review studies where proteomics has been applied to identify prognostic, predictive and therapeutic biomarkers. These studies traverse a range of histological subtypes including chordoma, Ewing sarcoma, gastrointestinal stromal tumors, leiomyosarcoma, liposarcoma, malignant peripheral nerve sheath tumors, myxofibrosarcoma, rhabdomyosarcoma, synovial sarcoma, osteosarcoma, and undifferentiated pleomorphic sarcoma. Critical questions and unmet needs in sarcoma which can potentially be addressed with proteomics are outlined. Frontiers Media S.A. 2023-05-01 /pmc/articles/PMC10183589/ /pubmed/37197427 http://dx.doi.org/10.3389/fonc.2023.1126736 Text en Copyright © 2023 Connolly, Grimison, Horvath, Robinson and Reddel https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Connolly, Elizabeth A. Grimison, Peter S. Horvath, Lisa G. Robinson, Phillip J. Reddel, Roger R. Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title | Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title_full | Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title_fullStr | Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title_full_unstemmed | Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title_short | Quantitative proteomic studies addressing unmet clinical needs in sarcoma |
title_sort | quantitative proteomic studies addressing unmet clinical needs in sarcoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183589/ https://www.ncbi.nlm.nih.gov/pubmed/37197427 http://dx.doi.org/10.3389/fonc.2023.1126736 |
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