Musani Vesna, Sabol Maja, Car Diana, Ozretic Petar, Oreskovic Slavko, Leovic Dinko, Levanat Sonja
Division of Molecular Medicine, Rudjer Boskovic Institute, Zagreb, Croatia.
Front Biosci (Elite Ed). 2012 Jan 1;4(3):1049-57. doi: 10.2741/E440.
Loss of heterozygosity (LOH) of tumor suppressor genes is a frequent event in tumorigenesis. LOH is most often analyzed by microsatellite typing, but here we offer a fast and efficient method for simultaneous SNP genotyping and mutation scanning, which can also be used for LOH detection. High resolution melting (HRM) provides simple variant detection, and can be adopted for a wide range of applications. When a melting profile for a specific SNP is determined, the screening can be done without the need for sequencing, and only the melting profiles differing from the established melting profiles should be sequenced. LOH of PTCH1 gene is often found in a series of different tumors, for example basal cell carcinoma (BCC) and ovarian carcinoma (OC). In this study LOH was detected in 50 % of BCC and 27.27 % of OC, and the detection rates of microsatellite typing and HRM were comparable. Both methods depended only on the heterozygosity of the loci analyzed, but HRM offers an additional advantage of detection of all sequence variants in the gene of interest.
肿瘤抑制基因的杂合性缺失(LOH)在肿瘤发生过程中是常见事件。LOH最常通过微卫星分型进行分析,但在此我们提供一种快速有效的方法用于同时进行单核苷酸多态性(SNP)基因分型和突变扫描,该方法也可用于LOH检测。高分辨率熔解曲线分析(HRM)提供了简单的变异检测,可用于广泛的应用。当确定特定SNP的熔解曲线时,无需测序即可进行筛查,仅对与已建立的熔解曲线不同的熔解曲线进行测序。PTCH1基因的LOH在一系列不同肿瘤中经常被发现,例如基底细胞癌(BCC)和卵巢癌(OC)。在本研究中,在50%的BCC和27.27%的OC中检测到LOH,微卫星分型和HRM的检测率相当。两种方法都仅依赖于所分析位点的杂合性,但HRM还具有检测目标基因中所有序列变异的额外优势。