Ebinger M, Sotlar K, Weber A, Bock C T, Bültmann B D, Kandolf R
Department of Haematology and Oncology, Children's Hospital, University of Tübingen, Tübingen, Germany.
J Clin Pathol. 2006 Oct;59(10):1114-5. doi: 10.1136/jcp.2005.028217.
A panel of five quasimonomorphic mononucleotide repeats that dispenses with the need to analyse corresponding germline DNA was proposed by Suraweera et al for the detection of high-frequency microsatellite instability (MSI) in colorectal cancer. Using this panel, a simplified and a more sensitive (compared with the original) algorithm (p<0.05) was developed to define the instability of each repeat by assessing the morphological shape of its plot and not its absolute length. 103 cases of colorectal tumours were investigated and the results compared with those obtained by the analysis of five consensus microsatellites (Bethesda reference panel). By the proposed method, a higher specificity, but no loss of sensitivity, was found. Thus, the use of the five mononucleotide repeats in combination with the modified assessment technique simplifies the assessment of MSI, while retaining the sensitivity of the Bethesda panel for the detection of high-frequency MSI.
Suraweera等人提出了一组五个准单态单核苷酸重复序列,无需分析相应的种系DNA即可检测结直肠癌中的高频微卫星不稳定性(MSI)。使用该组重复序列,开发了一种简化且更灵敏(与原始方法相比,p<0.05)的算法,通过评估其图谱的形态形状而非绝对长度来定义每个重复序列的不稳定性。对103例结直肠肿瘤病例进行了研究,并将结果与通过分析五个一致性微卫星(贝塞斯达参考组)获得的结果进行比较。通过所提出的方法,发现具有更高的特异性,但不损失敏感性。因此,将五个单核苷酸重复序列与改良的评估技术结合使用,简化了MSI的评估,同时保留了贝塞斯达组检测高频MSI的敏感性。