Yamamoto Go, Nannya Yasuhito, Kato Motohiro, Sanada Masashi, Levine Ross L, Kawamata Norihiko, Hangaishi Akira, Kurokawa Mineo, Chiba Shigeru, Gilliland D Gary, Koeffler H Phillip, Ogawa Seishi
Departments of Hematology and Oncology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Am J Hum Genet. 2007 Jul;81(1):114-26. doi: 10.1086/518809. Epub 2007 Jun 5.
Loss of heterozygosity (LOH), either with or without accompanying copy-number loss, is a cardinal feature of cancer genomes that is tightly linked to cancer development. However, detection of LOH is frequently hampered by the presence of normal cell components within tumor specimens and the limitation in availability of constitutive DNA. Here, we describe a simple but highly sensitive method for genomewide detection of allelic composition, based on the Affymetrix single-nucleotide-polymorphism genotyping microarray platform, without dependence on the availability of constitutive DNA. By sensing subtle distortions in allele-specific signals caused by allelic imbalance with the use of anonymous controls, sensitive detection of LOH is enabled with accurate determination of allele-specific copy numbers, even in the presence of up to 70%-80% normal cell contamination. The performance of the new algorithm, called "AsCNAR" (allele-specific copy-number analysis using anonymous references), was demonstrated by detecting the copy-number neutral LOH, or uniparental disomy (UPD), in a large number of acute leukemia samples. We next applied this technique to detection of UPD involving the 9p arm in myeloproliferative disorders (MPDs), which is tightly associated with a homozygous JAK2 mutation. It revealed an unexpectedly high frequency of 9p UPD that otherwise would have been undetected and also disclosed the existence of multiple subpopulations having distinct 9p UPD within the same MPD specimen. In conclusion, AsCNAR should substantially improve our ability to dissect the complexity of cancer genomes and should contribute to our understanding of the genetic basis of human cancers.
杂合性缺失(LOH),无论是否伴有拷贝数丢失,都是癌症基因组的一个主要特征,与癌症发展紧密相关。然而,肿瘤标本中正常细胞成分的存在以及组成性DNA可用性的限制,常常阻碍了LOH的检测。在此,我们描述了一种基于Affymetrix单核苷酸多态性基因分型微阵列平台的简单但高度灵敏的全基因组等位基因组成检测方法,该方法不依赖组成性DNA的可用性。通过使用匿名对照来感知由等位基因不平衡引起的等位基因特异性信号的细微扭曲,即使存在高达70%-80%的正常细胞污染,也能够准确测定等位基因特异性拷贝数,从而灵敏地检测LOH。通过检测大量急性白血病样本中的拷贝数中性LOH或单亲二体(UPD),证明了名为“AsCNAR”(使用匿名参考进行等位基因特异性拷贝数分析)的新算法的性能。接下来,我们将该技术应用于检测骨髓增殖性疾病(MPD)中涉及9p臂的UPD,其与纯合JAK2突变紧密相关。结果显示9p UPD的频率出乎意料地高,否则这些UPD可能无法被检测到,并且还揭示了在同一MPD标本中存在具有不同9p UPD的多个亚群。总之,AsCNAR应能大幅提高我们剖析癌症基因组复杂性的能力,并有助于我们理解人类癌症的遗传基础。