Ley Timothy J, Mardis Elaine R, Ding Li, Fulton Bob, McLellan Michael D, Chen Ken, Dooling David, Dunford-Shore Brian H, McGrath Sean, Hickenbotham Matthew, Cook Lisa, Abbott Rachel, Larson David E, Koboldt Dan C, Pohl Craig, Smith Scott, Hawkins Amy, Abbott Scott, Locke Devin, Hillier Ladeana W, Miner Tracie, Fulton Lucinda, Magrini Vincent, Wylie Todd, Glasscock Jarret, Conyers Joshua, Sander Nathan, Shi Xiaoqi, Osborne John R, Minx Patrick, Gordon David, Chinwalla Asif, Zhao Yu, Ries Rhonda E, Payton Jacqueline E, Westervelt Peter, Tomasson Michael H, Watson Mark, Baty Jack, Ivanovich Jennifer, Heath Sharon, Shannon William D, Nagarajan Rakesh, Walter Matthew J, Link Daniel C, Graubert Timothy A, DiPersio John F, Wilson Richard K
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63108, USA.
Nature. 2008 Nov 6;456(7218):66-72. doi: 10.1038/nature07485.
Acute myeloid leukaemia is a highly malignant haematopoietic tumour that affects about 13,000 adults in the United States each year. The treatment of this disease has changed little in the past two decades, because most of the genetic events that initiate the disease remain undiscovered. Whole-genome sequencing is now possible at a reasonable cost and timeframe to use this approach for the unbiased discovery of tumour-specific somatic mutations that alter the protein-coding genes. Here we present the results obtained from sequencing a typical acute myeloid leukaemia genome, and its matched normal counterpart obtained from the same patient's skin. We discovered ten genes with acquired mutations; two were previously described mutations that are thought to contribute to tumour progression, and eight were new mutations present in virtually all tumour cells at presentation and relapse, the function of which is not yet known. Our study establishes whole-genome sequencing as an unbiased method for discovering cancer-initiating mutations in previously unidentified genes that may respond to targeted therapies.
急性髓系白血病是一种高度恶性的造血肿瘤,在美国每年影响约13000名成年人。在过去二十年中,这种疾病的治疗方法变化不大,因为引发该疾病的大多数基因事件仍未被发现。现在,以合理的成本和时间框架进行全基因组测序成为可能,从而能够利用这种方法无偏见地发现改变蛋白质编码基因的肿瘤特异性体细胞突变。在此,我们展示了对一个典型急性髓系白血病基因组及其从同一患者皮肤获取的匹配正常对照进行测序所得到的结果。我们发现了十个发生获得性突变的基因;其中两个是先前已描述的、被认为有助于肿瘤进展的突变,另外八个是在初诊和复发时几乎所有肿瘤细胞中都存在的新突变,其功能尚不清楚。我们的研究确立了全基因组测序作为一种无偏见的方法,用于在可能对靶向治疗有反应的先前未鉴定基因中发现癌症起始突变。