Nagayama Satoshi, Katagiri Toyomasa, Tsunoda Tatsuhiko, Hosaka Taisuke, Nakashima Yasuaki, Araki Nobuhito, Kusuzaki Katsuyuki, Nakayama Tomitaka, Tsuboyama Tadao, Nakamura Takashi, Imamura Masayuki, Nakamura Yusuke, Toguchida Junya
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Japan.
Cancer Res. 2002 Oct 15;62(20):5859-66.
Among a histologically heterogeneous group of soft tissue sarcomas, synovial sarcoma (SS) is regarded as a "miscellaneous" entity of uncertain origin. Although recent molecular analysis has disclosed involvement of a specific chromosomal translocation in the pathogenesis of SS, its genetic features remain largely unclear. In the work reported here we examined genome-wide gene expression profiles of 13 SS cases and 34 other spindle-cell sarcoma cases by cDNA microarray consisting of 23,040 genes. A hierarchical clustering analysis grouped SS and malignant peripheral nerve sheath tumor into the same category, and these two types of tumor shared expression patterns of numerous genes relating to neural differentiation. Several genes were up-regulated in almost all SS cases, and the presumed functions of known genes among them were related to migration or differentiation of neural crest cells, suggesting the possibility of neuroectodermal origin of SS. Moreover, we identified a set of genes that divided SS cases into two putative subclasses, a feature that may shed light on novel biological aspects of SS in addition to those having to do with epithelial differentiation. These data have provided clues for understanding the origin and tumorigenesis of SS.
在一组组织学上异质性的软组织肉瘤中,滑膜肉瘤(SS)被视为起源不明的“混杂”实体。尽管最近的分子分析已揭示一种特定的染色体易位参与了滑膜肉瘤的发病机制,但其遗传特征仍 largely 不清楚。在本文报道的研究中,我们通过包含 23,040 个基因的 cDNA 微阵列检测了 13 例滑膜肉瘤病例和 34 例其他梭形细胞肉瘤病例的全基因组基因表达谱。层次聚类分析将滑膜肉瘤和恶性外周神经鞘瘤归为同一类别,并且这两种肿瘤共享许多与神经分化相关基因的表达模式。几乎在所有滑膜肉瘤病例中,有几个基因上调,其中已知基因的推测功能与神经嵴细胞的迁移或分化有关,提示滑膜肉瘤可能起源于神经外胚层。此外,我们鉴定出一组基因,可将滑膜肉瘤病例分为两个假定的亚类,这一特征除了与上皮分化相关的方面外,可能还为滑膜肉瘤新的生物学特性提供线索。这些数据为理解滑膜肉瘤的起源和肿瘤发生提供了线索。