Navarro M, Simon M P, Migeon C, Turc-Carel C, Pedeutour F
Laboratoire de Génétique Chromosomique des Tumeurs, UMR 4569, Faculté de Médecine, Nice, France.
Genes Chromosomes Cancer. 1998 Nov;23(3):263-6.
Dermatofibrosarcoma protuberans (DP), an infiltrative skin tumor of intermediate malignancy, presents specific cytogenetic features such as reciprocal translocations t(17;22)(q22;q13.1) or, more often, supernumerary ring chromosomes derived from t(17;22). Different translocations, including t(2;17) and t(X;7), have also been described. We have shown previously that both r(17;22) and t(17;22) present the same molecular rearrangement fusing the COL1A1 gene on chromosome 17 and the PDGFB gene on chromosome 22. Out of our series of 16 DPs, we detected an extra ring chromosome in tumor T96-1175, which juxtaposed sequences from chromosomes 4 and 17. As shown by fluorescence in situ hybridization (FISH) using chromosome painting and alpha-satellite probes, T96-1175 apparently lacked chromosome 22 material in the ring. However, involvement of chromosome 22 through a rearrangement of PDGFB was shown by Southern blotting, reverse transcriptase-polymerase chain reaction (RT-PCR), and FISH. This study demonstrates that a cryptic molecular rearrangement between chromosomes 17 and 22 occurred in addition to the recombination of chromosomes 4 and 17 initially identified by FISH. Assessment for cryptic molecular events should be performed in other variant DP rearrangements.
隆突性皮肤纤维肉瘤(DP)是一种中度恶性的浸润性皮肤肿瘤,具有特定的细胞遗传学特征,如相互易位t(17;22)(q22;q13.1),或更常见的源自t(17;22)的额外环状染色体。也有其他易位的报道,包括t(2;17)和t(X;7)。我们之前已经表明,r(17;22)和t(17;22)呈现相同的分子重排,即17号染色体上的COL1A1基因与22号染色体上的PDGFB基因融合。在我们的16例DP病例系列中,我们在肿瘤T96 - 1175中检测到一条额外的环状染色体,它并列了4号和17号染色体的序列。使用染色体涂染和α卫星探针的荧光原位杂交(FISH)显示,T96 - 1175的环状染色体中明显缺乏22号染色体物质。然而,通过Southern印迹、逆转录聚合酶链反应(RT-PCR)和FISH显示,22号染色体通过PDGFB重排而受累。这项研究表明,除了最初通过FISH鉴定的4号和17号染色体重组外,17号和22号染色体之间还发生了隐匿的分子重排。对于隐匿分子事件的评估应在其他变异的DP重排中进行。