Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy

Synovial sarcoma (SS), an aggressive type of soft tissue tumor, occurs mostly in adolescents and young adults. The origin and molecular mechanism of the development of SS remain only partially known. Over 90% of SS cases are characterized by the t(X;18)(p11.2;q11.2) translocation, which results main...

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Main Authors: Joanna Przybyl, Monika Jurkowska, Piotr Rutkowski, Maria Debiec-Rychter, Janusz A. Siedlecki
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Sarcoma
Online Access:http://dx.doi.org/10.1155/2012/249219
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spelling doaj-1c7d796b98844c898a58ca885c12e0652020-11-24T23:55:13ZengHindawi LimitedSarcoma1357-714X1369-16432012-01-01201210.1155/2012/249219249219Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted TherapyJoanna Przybyl0Monika Jurkowska1Piotr Rutkowski2Maria Debiec-Rychter3Janusz A. Siedlecki4Department of Molecular Biology, The Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, 02-781 Warsaw, PolandDepartment of Molecular Diagnostics Laboratory, The Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone Sarcoma and Melanoma, The Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, 02-781 Warsaw, PolandDepartment of Human Genetics, Catholic University of Leuven, 3000 Leuven, BelgiumDepartment of Molecular Biology, The Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, 02-781 Warsaw, PolandSynovial sarcoma (SS), an aggressive type of soft tissue tumor, occurs mostly in adolescents and young adults. The origin and molecular mechanism of the development of SS remain only partially known. Over 90% of SS cases are characterized by the t(X;18)(p11.2;q11.2) translocation, which results mainly in the formation of SS18-SSX1 or SS18-SSX2 fusion genes. In recent years, several reports describing direct and indirect interactions of SS18-SSX1/SSX2 oncoproteins have been published. These reports suggest that the fusion proteins particularly affect the cell growth, cell proliferation, TP53 pathway, and chromatin remodeling mechanisms, contributing to SS oncogenesis. Additional research efforts are required to fully explore the protein-protein interactions of SS18-SSX oncoproteins and the pathways that are regulated by these partnerships for the development of effective targeted therapy.http://dx.doi.org/10.1155/2012/249219
collection DOAJ
language English
format Article
sources DOAJ
author Joanna Przybyl
Monika Jurkowska
Piotr Rutkowski
Maria Debiec-Rychter
Janusz A. Siedlecki
spellingShingle Joanna Przybyl
Monika Jurkowska
Piotr Rutkowski
Maria Debiec-Rychter
Janusz A. Siedlecki
Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
Sarcoma
author_facet Joanna Przybyl
Monika Jurkowska
Piotr Rutkowski
Maria Debiec-Rychter
Janusz A. Siedlecki
author_sort Joanna Przybyl
title Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
title_short Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
title_full Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
title_fullStr Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
title_full_unstemmed Downstream and Intermediate Interactions of Synovial Sarcoma-Associated Fusion Oncoproteins and Their Implication for Targeted Therapy
title_sort downstream and intermediate interactions of synovial sarcoma-associated fusion oncoproteins and their implication for targeted therapy
publisher Hindawi Limited
series Sarcoma
issn 1357-714X
1369-1643
publishDate 2012-01-01
description Synovial sarcoma (SS), an aggressive type of soft tissue tumor, occurs mostly in adolescents and young adults. The origin and molecular mechanism of the development of SS remain only partially known. Over 90% of SS cases are characterized by the t(X;18)(p11.2;q11.2) translocation, which results mainly in the formation of SS18-SSX1 or SS18-SSX2 fusion genes. In recent years, several reports describing direct and indirect interactions of SS18-SSX1/SSX2 oncoproteins have been published. These reports suggest that the fusion proteins particularly affect the cell growth, cell proliferation, TP53 pathway, and chromatin remodeling mechanisms, contributing to SS oncogenesis. Additional research efforts are required to fully explore the protein-protein interactions of SS18-SSX oncoproteins and the pathways that are regulated by these partnerships for the development of effective targeted therapy.
url http://dx.doi.org/10.1155/2012/249219
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