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通过荧光原位杂交技术检测多形性腺瘤中的隐匿性结构重排

Detection of hidden structural rearrangements by FISH in pleomorphic adenomas.

作者信息

Sahlin P, Mark J, Stenman G

机构信息

Department of Pathology, Göteborg University, Sweden.

出版信息

Genes Chromosomes Cancer. 1995 Feb;12(2):81-6. doi: 10.1002/gcc.2870120202.

Abstract

Previous cytogenetic analysis of pleomorphic adenomas of the salivary glands has revealed a subgroup of tumors with interstitial deletions of 8q with breakpoints at q12 and q21-23. In this paper we have re-examined four adenomas with confirmed or suspected deletions of 8q by FISH. Painting of interphase nuclei and metaphase chromosomes with whole chromosome libraries revealed that in each of the four cases the deleted chromosome 8 material was found inserted or translocated onto other chromosomes. In two of the cases we were also able to resolve several other complex rearrangements. Our FISH data thus suggest that gross deletions of 8q do not occur in pleomorphic adenomas. These observations are of crucial importance for the molecular interpretations of the 8q12 rearrangements. The fact that all rearrangements with breakpoints at 8q12 seem to be translocations or insertions strongly indicates that they involve a similar molecular mechanism. Our findings illustrate that chromosome painting is a valuable and useful adjunct to conventional cytogenetic analysis of solid tumors.

摘要

以往对涎腺多形性腺瘤的细胞遗传学分析显示,存在一个肿瘤亚群,其8号染色体长臂(8q)存在间质性缺失,断点位于q12和q21 - 23。在本文中,我们通过荧光原位杂交(FISH)对4例已确认或疑似8q缺失的腺瘤进行了重新检测。用全染色体文库对间期核和中期染色体进行描绘显示,在这4例中的每一例中,均发现缺失的8号染色体物质插入或易位到了其他染色体上。在其中2例中,我们还能够解析其他几种复杂的重排。因此,我们的FISH数据表明,8q的大片段缺失在多形性腺瘤中并不发生。这些观察结果对于8q12重排的分子解释至关重要。所有断点位于8q12的重排似乎都是易位或插入这一事实强烈表明,它们涉及相似的分子机制。我们的研究结果表明,染色体描绘是实体瘤传统细胞遗传学分析的一种有价值且有用的辅助手段。

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