在黑素细胞肿瘤的FISH诊断解释中涉及的挑战

Chelsea Cooper, L. Sholl, P. Gerami
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引用次数: 0

摘要

在分子水平上,黑色素瘤和痣表现出明显的染色体拷贝数畸变。因此,诸如FISH之类的分子技术的加入可能会改善黑色素细胞肿瘤的诊断程序。FISH探针靶向6p25、11q13、6q23、9p21、8q24和CEP 6,目前用于黑色素瘤的诊断。虽然这些分析方法非常实用,但在优化解释方面可能会出现挑战。在这篇综述中,作者讨论了通常与FISH协议相关的技术挑战,如消化过度、消化不足和过量的背景。作者还提出了与FISH解释染色体拷贝数变化相关的挑战,并就如何将这些困难的影响降至最低提出了建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges involved in the diagnostic interpretation of FISH for melanocytic neoplasms
At the molecular level, melanoma and nevi exhibit distinct chromosomal copy number aberrations. As a result, the addition of molecular techniques such as FISH may improve the diagnostic procedures for melanocytic neoplasms. FISH probes targeting 6p25, 11q13, 6q23, 9p21, 8q24 and CEP 6 are currently used in the diagnosis of melanoma. While these assays can be of great utility, there are challenges that may emerge in optimizing interpretation. In this review, the authors discuss technical challenges commonly associated with the FISH protocol such as overdigestion, underdigestion and excessive background. The authors also present challenges associated with interpretation of the FISH for chromosomal copy number changes and offer suggestions as to how the effects of these difficulties can be minimized.
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