Map kinase signaling pathways and hematologic malignancies

被引:362
作者
Platanias, LC
机构
[1] Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Div Hematol Oncol, Chicago, IL 60611 USA
关键词
D O I
10.1182/blood-2002-12-3647
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitogen-activated protein (Map) kinases are widely expressed serine-threonine kinases that mediate important regulatory signals in the cell. Three major groups of Map kinases exist: the p38 Map kinase family, the extracellular signal-regulated kinase (Erk) family, and the c-Jun NH2-terminal kinase (JNK) family. The members of the different Map kinase groups participate in the generation of various cellular responses, including gene transcription, induction of cell death or maintenance of cell survival, malignant transformation, and regulation of cell-cycle progression. Depending on the specific family isoform involved and the cellular context, Map kinase pathways can mediate signals that either promote or suppress the growth of malignant hematopoietic cells. Over the last few years, extensive work by several groups has established that Map kinase pathways play critical roles in the pathogenesis of various hematologic malignancies, providing new molecular targets for future therapeutic approaches. In this review, the involvement of various Map kinase pathways in the pathophysiology of hematologic malignances is summarized and the clinical implications of the recent advances in the field are discussed. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:4667 / 4679
页数:13
相关论文
共 209 条
[11]   BIOLOGIC EFFECTS OF ANTI-INTERLEUKIN-6 MURINE MONOCLONAL-ANTIBODY IN ADVANCED MULTIPLE-MYELOMA [J].
BATAILLE, R ;
BARLOGIE, B ;
LU, ZY ;
ROSSI, JF ;
LAVABREBERTRAND, T ;
BECK, T ;
WIJDENES, J ;
BROCHIER, J ;
KLEIN, B .
BLOOD, 1995, 86 (02) :685-691
[12]   SERUM LEVELS OF INTERLEUKIN-6, A POTENT MYELOMA CELL-GROWTH FACTOR, AS A REFLECT OF DISEASE SEVERITY IN PLASMA-CELL DYSCRASIAS [J].
BATAILLE, R ;
JOURDAN, M ;
ZHANG, XG ;
KLEIN, B .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (06) :2008-2011
[13]   Combined effects of aberrant MEK1 activity and BCL2 overexpression on relieving the cytokine dependency of human and murine hematopoietic cells [J].
Blalock, WL ;
Moye, PW ;
Chang, F ;
Pearce, M ;
Steelman, LS ;
McMahon, M ;
McCubrey, JA .
LEUKEMIA, 2000, 14 (06) :1080-1096
[14]   A conditionally-active form of MEK1 results in autocrine transformation of human and mouse hematopoietic cells [J].
Blalock, WL ;
Pearce, M ;
Steelman, LS ;
Franklin, RA ;
McCarthy, SA ;
Cherwinski, H ;
McMahon, M ;
McCubrey, JA .
ONCOGENE, 2000, 19 (04) :526-536
[15]   Molecular cloning of mitogen-activated protein ERK kinase kinases (MEKK) 2 and 3 - Regulation of sequential phosphorylation pathways involving mitogen-activated protein kinase and c-Jun kinase [J].
Blank, JL ;
Gerwins, P ;
Elliott, EM ;
Sather, S ;
Johnson, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5361-5368
[16]  
BOS JL, 1987, BLOOD, V69, P1237
[17]   AN INSULIN-STIMULATED PROTEIN-KINASE SIMILAR TO YEAST KINASES INVOLVED IN CELL-CYCLE CONTROL [J].
BOULTON, TG ;
YANCOPOULOS, GD ;
GREGORY, JS ;
SLAUGHTER, C ;
MOOMAW, C ;
HSU, J ;
COBB, MH .
SCIENCE, 1990, 249 (4964) :64-67
[18]   ERKS - A FAMILY OF PROTEIN-SERINE THREONINE KINASES THAT ARE ACTIVATED AND TYROSINE PHOSPHORYLATED IN RESPONSE TO INSULIN AND NGF [J].
BOULTON, TG ;
NYE, SH ;
ROBBINS, DJ ;
IP, NY ;
RADZIEJEWSKA, E ;
MORGENBESSER, SD ;
DEPINHO, RA ;
PANAYOTATOS, N ;
COBB, MH ;
YANCOPOULOS, GD .
CELL, 1991, 65 (04) :663-675
[19]  
BROXMEYER HE, 1983, J IMMUNOL, V131, P1300
[20]  
BROXMEYER HE, 1985, J IMMUNOL, V135, P2502