Jensen Lars Henrik, Cruger Dorthe G, Lindebjerg Jan, Byriel Lene, Bruun-Petersen Gert, Jakobsen Anders
Danish Colorectal Cancer Group South, University of Southern Denmark, Vejle Hospital, Vejle, Denmark.
Anticancer Res. 2006 May-Jun;26(3A):2069-74.
Microsatellite instability (MSI) is an important marker in colorectal cancer. The analysis may be difficult if the tumour is heterogeneous or only scarce material is available. The aim of this study was to apply laser microdissection (LMD) to MSI analysis in an attempt to allow diagnosis in these situations.
Twenty-two primary tumours and eight lymph node metastases from twenty patients were laser microdissected and MSI analysis was performed with an optimised multiplex PCR. Differences in allelic size between tumour and blood were evaluated to determine the MSI status.
The method proved efficient in as little as 4,000 microm3 formalin-treated and paraffin-embedded tumour tissue. The result of microsatellite analysis was independent of sample location in the primary tumour and its metastasis.
LMD followed by a multiplex PCR is a useful method for MSI analysis in cases of tumour heterogeneity and scarce tumour material.
微卫星不稳定性(MSI)是结直肠癌的一个重要标志物。如果肿瘤具有异质性或仅能获得少量材料,分析可能会很困难。本研究的目的是将激光显微切割(LMD)应用于MSI分析,试图在这些情况下进行诊断。
对20例患者的22个原发性肿瘤和8个淋巴结转移灶进行激光显微切割,并用优化的多重PCR进行MSI分析。评估肿瘤与血液之间等位基因大小的差异以确定MSI状态。
该方法在仅4000立方微米的经福尔马林处理并石蜡包埋的肿瘤组织中就证明是有效的。微卫星分析结果与原发性肿瘤及其转移灶中的样本位置无关。
对于肿瘤异质性和肿瘤材料稀缺的情况,LMD联合多重PCR是一种用于MSI分析的有用方法。