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青少年骨髓单核细胞白血病:第二届国际青少年骨髓单核细胞白血病研讨会报告

Juvenile myelomonocytic leukemia: a report from the 2nd International JMML Symposium.

作者信息

Chan Rebecca J, Cooper Todd, Kratz Christian P, Weiss Brian, Loh Mignon L

机构信息

Departments of Pediatrics, The Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Leuk Res. 2009 Mar;33(3):355-62. doi: 10.1016/j.leukres.2008.08.022. Epub 2008 Oct 26.

Abstract

Juvenile myelomonocytic leukemia (JMML) is an aggressive childhood myeloproliferative disorder characterized by the overproduction of myelomonocytic cells. JMML incidence approaches 1.2/million persons in the United States (Cancer Incidence and Survival Among Children and Adolescents: United States SEER Program 1975-1995). Although rare, JMML is innately informative as the molecular genetics of this disease implicates hyperactive Ras as an essential initiating event. Given that Ras is one of the most frequently mutated oncogenes in human cancer, findings from this disease are applicable to more genetically diverse and complex adult leukemias. The JMML Foundation (www.jmmlfoundation.org) was founded by parent advocates dedicated to finding a cure for this disease. They work to bring investigators together in a collaborative manner. This article summarizes key presentations from The Second International JMML Symposium, on 7-8 December 2007 in Atlanta, GA. A list of all participants is in Supplementary Table.

摘要

青少年粒单核细胞白血病(JMML)是一种侵袭性儿童骨髓增殖性疾病,其特征是粒单核细胞过度产生。在美国,JMML的发病率接近每百万人中有1.2例(《儿童和青少年的癌症发病率与生存率:美国监测、流行病学和最终结果计划1975 - 1995》)。尽管罕见,但JMML在本质上具有重要意义,因为这种疾病的分子遗传学表明,过度活跃的Ras是一个关键的起始事件。鉴于Ras是人类癌症中最常发生突变的癌基因之一,该疾病的研究结果适用于更多基因多样且复杂的成人白血病。JMML基金会(www.jmmlfoundation.org)由致力于找到治愈这种疾病方法的患儿家长倡导者创立。他们致力于以合作的方式将研究人员聚集在一起。本文总结了2007年12月7 - 8日在佐治亚州亚特兰大举行的第二届国际JMML研讨会上的主要报告。所有参会人员名单见补充表。

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1
Leukemogenic Ptpn11 causes fatal myeloproliferative disorder via cell-autonomous effects on multiple stages of hematopoiesis.
Blood. 2009 Apr 30;113(18):4414-24. doi: 10.1182/blood-2008-10-182626. Epub 2009 Jan 29.
4
Recent advances in the pathogenesis and management of juvenile myelomonocytic leukaemia.
Br J Haematol. 2008 May;141(5):567-75. doi: 10.1111/j.1365-2141.2008.07104.x. Epub 2008 Apr 13.
6
Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations.
Blood. 2008 Jan 15;111(2):966-7; author reply 967-8. doi: 10.1182/blood-2007-09-111831.
7
Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia.
Blood. 2008 Feb 1;111(3):1124-7. doi: 10.1182/blood-2007-06-093302. Epub 2007 Nov 13.
8
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
Nat Genet. 2007 Aug;39(8):1007-12. doi: 10.1038/ng2073. Epub 2007 Jul 1.
9
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
Nat Genet. 2007 Aug;39(8):1013-7. doi: 10.1038/ng2078. Epub 2007 Jul 1.
10

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