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

被引:116
作者
Chan, Rebecca J. [2 ]
Cooper, Todd [3 ]
Kratz, Christian P. [4 ]
Weiss, Brian [5 ]
Loh, Mignon L. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Indiana Univ, Sch Med, Dept Pediat, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[3] Univ Alabama Birmingham, Dept Pediat, Div Pediat Hematol Oncol, Birmingham, AL USA
[4] Univ Freiburg, Dept Pediat & Adolescent Med, Freiburg, Germany
[5] Univ Cincinnati, Med Ctr, Div Pediat Hematol Oncol, Dept Pediat,Cincinnati Childrens Hosp,Coll Med, Cincinnati, OH 45267 USA
基金
美国国家卫生研究院;
关键词
Juvenile myelomonocytic leukemia (JMML); RAS; PTPN11; NF1; Therapy; Diagnosis; STEM-CELL TRANSPLANTATION; GENOTYPE-PHENOTYPE CORRELATION; COLONY-STIMULATING FACTOR; MUTATIONS CAUSE NOONAN; OF-FUNCTION MUTATIONS; PTPN11; MUTATIONS; MYELOPROLIFERATIVE DISORDER; MYELODYSPLASTIC SYNDROMES; TYPE-1; NEUROFIBROMATOSIS; GERMLINE MUTATIONS;
D O I
10.1016/j.leukres.2008.08.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:355 / 362
页数:8
相关论文
共 59 条
[1]  
Allard JD, 1996, DEVELOPMENT, V122, P1137
[2]   JUVENILE CHRONIC GRANULOCYTIC LEUKEMIA - PANMYELOPATHY WITH PROMINENT MONOCYTIC INVOLVEMENT AND CIRCULATING MONOCYTE COLONY-FORMING CELLS [J].
ALTMAN, AJ ;
PALMER, CG ;
BAEHNER, RL .
BLOOD, 1974, 43 (03) :341-350
[3]   Germline mutations in HRAS proto-oncogene cause Costello syndrome [J].
Aoki, Y ;
Niihori, T ;
Kawame, H ;
Kurosawa, K ;
Filocamo, M ;
Kato, K ;
Suzuki, Y ;
Kure, S ;
Matsubara, Y .
NATURE GENETICS, 2005, 37 (10) :1038-1040
[4]   Development of an allele-specific minimal residual disease assay for patients with juvenile myelomonocytic leukemia [J].
Archambeault, Sophie ;
Flores, Nikki J. ;
Yoshimi, Ayami ;
Kratz, Christian P. ;
Reising, Miriam ;
Fischer, Alexandra ;
Noellke, Peter ;
Locatelli, Franco ;
Sedlacek, Petr ;
Flotho, Christian ;
Zecca, Marco ;
Emanuel, Peter D. ;
Castleberry, Robert P. ;
Niemeyer, Charlotte M. ;
Bader, Peter ;
Loh, Mignon L. .
BLOOD, 2008, 111 (03) :1124-1127
[5]   NEUROFIBROMATOSIS AND CHILDHOOD LEUKEMIA [J].
BADER, JL ;
MILLER, RW .
JOURNAL OF PEDIATRICS, 1978, 92 (06) :925-929
[6]   Occurrence of myeloproliferative disorder in patients with Noonan syndrome [J].
BaderMeunier, B ;
Tchernia, G ;
Mielot, F ;
Fontaine, JL ;
Thomas, C ;
Lyonnet, S ;
Lavergne, JM ;
Dommergues, JP .
JOURNAL OF PEDIATRICS, 1997, 130 (06) :885-889
[7]   ABERRANT REGULATION OF RAS PROTEINS IN MALIGNANT-TUMOR CELLS FROM TYPE-1 NEUROFIBROMATOSIS PATIENTS [J].
BASU, TN ;
GUTMANN, DH ;
FLETCHER, JA ;
GLOVER, TW ;
COLLINS, FS ;
DOWNWARD, J .
NATURE, 1992, 356 (6371) :713-715
[8]   Non-hematopoietic stem cell transplantation treatment of juvenile myelomonocytic leukemia: A retrospective analysis and definition of response criteria [J].
Bergstraesser, Eva ;
Hasle, Henrik ;
Rogge, Tim ;
Fischer, Alexandra ;
Zimmermann, Martin ;
Noellke, Peter ;
Niemeyer, Charlotte M. .
PEDIATRIC BLOOD & CANCER, 2007, 49 (05) :629-633
[9]   Nf1 and Gmcsf interact in myeloid leukemogenesis [J].
Birnbaum, RA ;
O'Marcaigh, A ;
Wardak, Z ;
Zhang, YY ;
Dranoff, G ;
Jacks, T ;
Clapp, DW ;
Shannon, KM .
MOLECULAR CELL, 2000, 5 (01) :189-195
[10]   Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cells [J].
Bollag, G ;
Clapp, DW ;
Shih, S ;
Adler, F ;
Zhang, YY ;
Thompson, P ;
Lange, BJ ;
Freedman, MH ;
McCormick, F ;
Jacks, T ;
Shannon, K .
NATURE GENETICS, 1996, 12 (02) :144-148