de Leeuw B, Suijkerbuijk R F, Olde Weghuis D, Meloni A M, Stenman G, Kindblom L G, Balemans M, van den Berg E, Molenaar W M, Sandberg A A
Department of Human Genetics, University Hospital, Nijmegen, The Netherlands.
Cancer Genet Cytogenet. 1994 Apr;73(2):89-94. doi: 10.1016/0165-4608(94)90191-0.
Fluorescence in situ hybridization (FISH) and molecular analyses of synovial sarcomas with cytogenetically similar (X;18)(p11.2;q11.2) translocations have revealed two alternative breakpoint regions in Xp11.2, one residing in the ornithine aminotransferase-like 1 (OATL1) region and the other one in the related but distinct OATL2 region. As these results were obtained by different groups, we set out to evaluate an extended series of tumors with special emphasis on the two possible X-related breakpoint regions. Together, seven synovial sarcomas were identified with a break in the OATL1 region and six with a break near OATL2, thereby confirming the actual existence of the two alternative Xp breakpoint regions. We speculate that there seems to be a relationship between the occurrence of these breakpoint regions and the histologic phenotype of the tumors, with a predominance of OATL1-related breakpoints in the classical biphasic tumors and of OATL2-related breakpoints in the monophasic fibrous tumors.
荧光原位杂交(FISH)以及对具有细胞遗传学相似的(X;18)(p11.2;q11.2)易位的滑膜肉瘤进行分子分析,结果显示在Xp11.2区域存在两个不同的断点区域,一个位于鸟氨酸转氨酶样1(OATL1)区域,另一个位于相关但不同的OATL2区域。由于这些结果是由不同的研究小组获得的,我们着手评估一系列范围更广的肿瘤,特别关注这两个可能与X相关的断点区域。总共鉴定出7例滑膜肉瘤,其断点位于OATL1区域,6例断点靠近OATL2,从而证实了这两个不同的Xp断点区域的实际存在。我们推测,这些断点区域的出现与肿瘤的组织学表型之间似乎存在某种关系,在经典的双相肿瘤中,与OATL1相关的断点占优势,而在单相纤维性肿瘤中,与OATL2相关的断点占优势。