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本文引用的文献

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Regularization Paths for Cox's Proportional Hazards Model via Coordinate Descent.通过坐标下降法求解Cox比例风险模型的正则化路径
J Stat Softw. 2011 Mar;39(5):1-13. doi: 10.18637/jss.v039.i05.
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Utility of peripheral blood for cytogenetic and mutation analysis in myelodysplastic syndrome.外周血在骨髓增生异常综合征的细胞遗传学和突变分析中的应用。
Blood. 2013 Jul 25;122(4):567-70. doi: 10.1182/blood-2012-12-471847. Epub 2013 Jun 12.
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The changing mutational landscape of acute myeloid leukemia and myelodysplastic syndrome.急性髓系白血病和骨髓增生异常综合征不断变化的突变特征。
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Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.成人新发急性髓系白血病的基因组和表观基因组图谱。
N Engl J Med. 2013 May 30;368(22):2059-74. doi: 10.1056/NEJMoa1301689. Epub 2013 May 1.
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Genomics-driven oncology: framework for an emerging paradigm.基因组学驱动的肿瘤学:新兴范例的框架。
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Lessons from the cancer genome.从癌症基因组中得到的启示。
Cell. 2013 Mar 28;153(1):17-37. doi: 10.1016/j.cell.2013.03.002.
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Cancer genome landscapes.肿瘤基因组图谱。
Science. 2013 Mar 29;339(6127):1546-58. doi: 10.1126/science.1235122.
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Clonal diversity of recurrently mutated genes in myelodysplastic syndromes.骨髓增生异常综合征中反复突变基因的克隆多样性。
Leukemia. 2013 Jun;27(6):1275-82. doi: 10.1038/leu.2013.58. Epub 2013 Feb 27.
9
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.非典型慢性髓性白血病中反复出现的 SETBP1 突变。
Nat Genet. 2013 Jan;45(1):18-24. doi: 10.1038/ng.2495. Epub 2012 Dec 9.
10
CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia.CUX1 是 7 号染色体上的一个杂合性缺失肿瘤抑制基因,在急性髓系白血病中经常失活。
Blood. 2013 Feb 7;121(6):975-83. doi: 10.1182/blood-2012-04-426965. Epub 2012 Dec 3.

骨髓增生异常综合征中驱动突变的临床和生物学意义。

Clinical and biological implications of driver mutations in myelodysplastic syndromes.

机构信息

Cancer Genome Project, Wellcome Trust Sanger Institute, Hinxton, United Kingdom;

出版信息

Blood. 2013 Nov 21;122(22):3616-27; quiz 3699. doi: 10.1182/blood-2013-08-518886. Epub 2013 Sep 12.

DOI:10.1182/blood-2013-08-518886
PMID:24030381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3837510/
Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of chronic hematological malignancies characterized by dysplasia, ineffective hematopoiesis and a variable risk of progression to acute myeloid leukemia. Sequencing of MDS genomes has identified mutations in genes implicated in RNA splicing, DNA modification, chromatin regulation, and cell signaling. We sequenced 111 genes across 738 patients with MDS or closely related neoplasms (including chronic myelomonocytic leukemia and MDS-myeloproliferative neoplasms) to explore the role of acquired mutations in MDS biology and clinical phenotype. Seventy-eight percent of patients had 1 or more oncogenic mutations. We identify complex patterns of pairwise association between genes, indicative of epistatic interactions involving components of the spliceosome machinery and epigenetic modifiers. Coupled with inferences on subclonal mutations, these data suggest a hypothesis of genetic "predestination," in which early driver mutations, typically affecting genes involved in RNA splicing, dictate future trajectories of disease evolution with distinct clinical phenotypes. Driver mutations had equivalent prognostic significance, whether clonal or subclonal, and leukemia-free survival deteriorated steadily as numbers of driver mutations increased. Thus, analysis of oncogenic mutations in large, well-characterized cohorts of patients illustrates the interconnections between the cancer genome and disease biology, with considerable potential for clinical application.

摘要

骨髓增生异常综合征(MDS)是一组异质性慢性血液系统恶性肿瘤,其特征为发育不良、无效造血以及向急性髓系白血病进展的风险可变。对 MDS 基因组进行测序已经鉴定出涉及 RNA 剪接、DNA 修饰、染色质调控和细胞信号转导的基因中的突变。我们对 738 例 MDS 或密切相关肿瘤(包括慢性髓单核细胞白血病和 MDS-骨髓增生性肿瘤)患者的 111 个基因进行了测序,以探讨获得性突变在 MDS 生物学和临床表型中的作用。78%的患者有 1 个或多个致癌突变。我们发现基因之间存在复杂的成对关联模式,表明涉及剪接体机制和表观遗传修饰物的成分的上位性相互作用。结合对亚克隆突变的推断,这些数据表明了遗传“宿命”的假说,其中早期驱动突变,通常影响涉及 RNA 剪接的基因,决定疾病进化的未来轨迹,具有不同的临床表型。驱动突变具有相同的预后意义,无论是克隆性还是亚克隆性,随着驱动突变数量的增加,白血病无复发生存率稳步下降。因此,对大型、特征明确的患者队列中的致癌突变进行分析说明了癌症基因组与疾病生物学之间的相互联系,具有很大的临床应用潜力。