使用MLPA方法对选定的中枢神经系统肿瘤进行分子病理分析。

Q4 Medicine
Ceskoslovenska patologie Pub Date : 2022-01-01
Iva Dolinová, Eliška Tvrzníková, Veronika Janoušková, Aleš Vícha, Lenka Krsková, Tomáš Jirásek
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引用次数: 0

摘要

目前的进展和对癌症遗传原因的不断增加的认识为其治疗开辟了新的可能性。然而,有必要将经典病理方法得到的结果与灵敏的、多元的分子病理方法结合起来。符合要求的方法是基于多重PCR反应的MLPA法。该方法检测基因拷贝数和DNA甲基化的变化,最后但并非最不重要的是,点突变。MLPA反应甚至适用于高度碎片化的DNA。同时,它是一种可靠的方法,可以在标准热循环仪上进行,荧光尖端标记需要自动测序仪。在一个反应中可以检测多达50个遗传标记,这个数字可以用于诊断和预后结论。所有这些特点使得MLPA分析不仅在诊断中被常规使用,而且在癌症研究中也被常规使用。本文旨在总结不同类型的MLPA反应,其好处,以及潜在的陷阱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular pathological profiling of selected tumors of the central nervous system using the MLPA method.

The current progress and increasing knowledge about the genetic causes of cancer opens up new possibilities for its treatment. However, it is necessary to combine the results obtained using classical pathological methods with sensitive, multiplex molecular pathological methods. The method that meets the required criteria is MLPA based on multiplex PCR reaction. This method detects both changes in gene copy number and DNA methylation and, last but not least, point mutations. The MLPA reaction is applicable to even highly fragmented DNA. At the same time, it is a robust method that can be performed on standard thermocyclers, the fluorescent tip label requires automatic sequencers. Up to 50 genetic markers can be tested in one reaction, a number that allows a diagnostic and prognostic conclusion. All these features lead to the routine use of MLPA analysis not only in diagnosis but also in cancer research. The present article aims to summarize the different types of MLPA reactions, its benefits, but also the potential pitfalls.

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来源期刊
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
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