| Literature DB >> 20198325 |
Satoshi Takenaka1, Norifumi Naka, Nobuhito Araki, Nobuyuki Hashimoto, Takafumi Ueda, Kiyoko Yoshioka, Hideki Yoshikawa, Kazuyuki Itoh.
Abstract
Synovial sarcoma (SS) is an aggressive soft-tissue malignancy characterized by a unique t(X;18) translocation resulting in expression of SS18-SSX fusion protein. In order to investigate the biological function of this fusion protein and to develop a novel therapeutic option, we examined downregulation of SS18-SSX1 expression by small interfering RNA targeting SS18-SSX1 in three human SS cell lines. Microarray analysis comparing SS18-SSX1-silenced cells with control cells in three SS cell lines showed that SS18-SSX1 mainly affected the focal adhesion pathway. In accord with the array data, silencing of SS18-SSX1 enhances adhesion to the extracellular matrix through the induction of expression of myosin light-chain kinase. Furthermore, the silencing of SS18-SSX1 inhibits anchorage-independent growth in vitro and systemic delivery of siRNA against SS18-SSX1 using a nanoparticle system inhibited tumor growth in a nude mouse xenograft model. Our results demonstrate that siRNA targeting of SS18-SSX1 has therapeutic potential for the treatment of SS.Entities:
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Year: 2010 PMID: 20198325 DOI: 10.3892/ijo_00000559
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650