Occurrence of an MLL/LAF4 fusion gene caused by the insertion ins(11;2)(q23;q11.2q11.2) in an infant with acute lymphoblastic leukemia

被引:15
作者
Bruch, J
Wilda, M
Teigler-Schlegel, A
Harbott, J
Borkhardt, A
Metzler, M
机构
[1] Childrens Univ Hosp Giessen, D-35392 Giessen, Germany
[2] Childrens Univ Hosp Erlangen, Erlangen, Germany
关键词
D O I
10.1002/gcc.10187
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:106 / 109
页数:4
相关论文
共 13 条
[1]   Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins [J].
Ayton, PM ;
Cleary, ML .
ONCOGENE, 2001, 20 (40) :5695-5707
[2]   Infant acute lymphoblastic leukemia - combined cytogenetic, immunophenotypical and molecular analysis of 77 cases [J].
Borkhardt, A ;
Wuchter, C ;
Viehmann, S ;
Pils, S ;
Teigler-Schlegel, A ;
Stanulla, M ;
Zimmermann, M ;
Ludwig, WD ;
Janka-Schaub, G ;
Schrappe, M ;
Harbott, J .
LEUKEMIA, 2002, 16 (09) :1685-1690
[3]   An ins(X;11)(q24;q23) fuses the MLL and the septin 6/KIAA0128 gene in an infant with AML-M2 [J].
Borkhardt, A ;
Teigler-Schlegel, A ;
Fuchs, U ;
Keller, C ;
König, M ;
Harbott, J ;
Haas, OA .
GENES CHROMOSOMES & CANCER, 2001, 32 (01) :82-88
[4]   The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia [J].
Fuchs, U ;
Rehkamp, G ;
Haas, OA ;
Slany, R ;
König, M ;
Bojesen, S ;
Bohle, RM ;
Damm-Welk, C ;
Ludwig, WD ;
Harbott, J ;
Borkhardt, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8756-8761
[5]   An atlas on chromosomes in hematological malignancies. Example: 11q23 and MLL partners [J].
Huret, JL ;
Dessen, P ;
Bernheim, A .
LEUKEMIA, 2001, 15 (06) :987-989
[6]   The "Atlas of Genetics and Cytogenetics in Oncology and Haematology" on the Internet and a review on infant leukemias [J].
Huret, JL ;
Dessen, P ;
Le Minor, S ;
Bernheim, A .
CANCER GENETICS AND CYTOGENETICS, 2000, 120 (02) :155-159
[7]   LAF-4 encodes a lymphoid nuclear protein with transactivation potential that is homologous to AF-4, the gene fused to MLL in t(4;11) leukemias [J].
Ma, C ;
Staudt, LM .
BLOOD, 1996, 87 (02) :734-745
[8]   MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site [J].
Slater, DJ ;
Hilgenfeld, E ;
Rappaport, EF ;
Shah, N ;
Meek, RG ;
Williams, WR ;
Lovett, BD ;
Osheroff, N ;
Autar, RS ;
Ried, T ;
Felix, CA .
ONCOGENE, 2002, 21 (30) :4706-4714
[9]   AF5q31, a newly identified AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia with ins(5;11)(q31;q13q23) [J].
Taki, T ;
Kano, H ;
Taniwaki, M ;
Sako, M ;
Yanagisawa, M ;
Hayashi, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14535-14540
[10]   REARRANGEMENT OF THE MLL GENE IN ACUTE LYMPHOBLASTIC AND ACUTE MYELOID LEUKEMIAS WITH 11Q23 CHROMOSOMAL TRANSLOCATIONS [J].
THIRMAN, MJ ;
GILL, HJ ;
BURNETT, RC ;
MBANGKOLLO, D ;
MCCABE, NR ;
KOBAYASHI, H ;
ZIEMINVANDERPOEL, S ;
KANEKO, Y ;
MORGAN, R ;
SANDBERG, AA ;
CHAGANTI, RSK ;
LARSON, RA ;
LEBEAU, MM ;
DIAZ, MO ;
ROWLEY, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (13) :909-914