Geurts van Kessel A, de Bruijn D, Hermsen L, Janssen I, dos Santos N R, Willems R, Makkus L, Schreuder H, Veth R
Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
Genes Chromosomes Cancer. 1998 Oct;23(2):198-201. doi: 10.1002/(sici)1098-2264(199810)23:2<198::aid-gcc15>3.3.co;2-h.
The initial cytogenetic analysis of a biphasic synovial sarcoma showed an apparently normal karyotype. After FISH using chromosome X- and 18-specific probes and RT-PCR using SYT- and SSX-specific primer sets, a cryptic synovial sarcoma-associated t(X;18)(p11;q11) could be revealed. The "masked" nature of the translocation may best be explained by a two-step scenario in which a genuine t(X;18)(p11;q11) has occurred as a first step and a reverse reciprocal X;18 translocation as a second step, leaving the synovial sarcoma-associated SYT-SSX1 fusion intact. The findings further underline our previous suggestion that SYT-SSX1 fusions may correlate with a biphasic nature of the tumor. In addition, our findings indicate that, in analogy to, e.g., the Philadelphia translocation in chronic myeloid leukemia, "masked" translocations may occur in soft tissue tumors and that, as a standard, RT-PCR and/or FISH analyses should be carried out in order to provide karyotypic information that may be relevant to tumor diagnosis and/or prognosis.
对双相滑膜肉瘤进行的初始细胞遗传学分析显示核型明显正常。使用X染色体和18号染色体特异性探针进行荧光原位杂交(FISH)以及使用SYT和SSX特异性引物组进行逆转录聚合酶链反应(RT-PCR)后,可揭示隐匿性滑膜肉瘤相关的t(X;18)(p11;q11)。这种易位的“隐匿”性质最好用两步情况来解释,第一步发生了真正的t(X;18)(p11;q11),第二步发生了反向相互的X;18易位,使滑膜肉瘤相关的SYT-SSX1融合保持完整。这些发现进一步强调了我们之前的观点,即SYT-SSX1融合可能与肿瘤的双相性质相关。此外,我们的发现表明,类似于慢性髓性白血病中的费城染色体易位,“隐匿”易位可能发生在软组织肿瘤中,并且作为标准操作,应该进行RT-PCR和/或FISH分析,以提供可能与肿瘤诊断和/或预后相关的核型信息。