Characterization of the MM.1 human multiple myeloma (MM) cell lines: A model system to elucidate the characteristics, behavior, and signaling of steroid-sensitive and -resistant MM cells

被引:123
作者
Greenstein, S
Krett, NL
Kurosawa, Y
Ma, CU
Chauhan, D
Hideshima, T
Anderson, KC
Rosen, ST
机构
[1] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Div Hematol Oncol,Dept Med, Chicago, IL 60611 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst,Dept Adult Oncol, Jerome Lipper Multiple Myeloma Ctr, Boston, MA 02115 USA
关键词
D O I
10.1016/S0301-472X(03)00023-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is a clonal B-lymphocyte malignancy, which is characterized by the accumulation of terminally differentiated antibody-producing cells in the bone marrow. Because current treatments offer only a median survival of 3 years, investigators continue to search for novel therapeutic strategies to combat the disease. Rational drug design is enhanced by understanding MM cell proliferation and key signaling pathways employed. In addition, a model system for preclinical evaluation of novel therapeutics is critical. Our laboratory has developed MM cell lines to study drug action and resistance, cell proliferation, and apoptosis. These cell lines are widely used in MM research. From a single MM patient, three separate cell lines were established that parallel the progression of the disease. These three cell lines, designated MM1S, MM1.R-E, and MM1.R-L, can be distinguished on the basis of their sensitivity to steroid hormones such as glucocorticoids (GCs). Utilization of these cell lines to study the etiology of MM, effects of chemotherapeutic agents, and development of clinical resistance, will provide us with vital information for the evolution of new and more efficacious therapeutics. The aim of this review is to summarize the morphological, biochemical, and growth characteristics of these cells, and to review the results from investigations of the MMA signaling pathways. This information will enhance the study, treatment, and eventual eradication of MM. (C) 2003 International Society for Experimental Hematology. Published by Elsevier Science Inc.
引用
收藏
页码:271 / 282
页数:12
相关论文
共 91 条
[1]  
ALEXANIAN R, 1994, NEW ENGL J MED, V330, P484
[2]  
ALEXANIAN R, 1992, BLOOD, V80, P887
[3]  
Astier A, 1997, J BIOL CHEM, V272, P228
[4]   The related adhesion focal tyrosine kinase differentially phosphorylates p130(Cas) and the Cas-like protein, p105(HEF1) [J].
Astier, A ;
Manie, SN ;
Avraham, H ;
Hirai, H ;
Law, SF ;
Zhang, YH ;
Golemis, EA ;
Fu, YG ;
Druker, BJ ;
Haghayeghi, N ;
Freedman, AS ;
Avraham, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19719-19724
[5]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[6]   RAFTK/Pyk2-mediated cellular signalling [J].
Avraham, H ;
Park, SY ;
Schinkmann, K ;
Avraham, S .
CELLULAR SIGNALLING, 2000, 12 (03) :123-133
[7]   IDENTIFICATION AND CHARACTERIZATION OF A NOVEL RELATED ADHESION FOCAL TYROSINE KINASE (RAFTK) FROM MEGAKARYOCYTES AND BRAIN [J].
AVRAHAM, S ;
LONDON, R ;
FU, YG ;
OTA, S ;
HIREGOWDARA, D ;
LI, JZ ;
JIANG, SX ;
PASZTOR, LN ;
WHITE, RA ;
GROOPMAN, JE ;
AVRAHAM, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27742-27751
[8]   Characterization of the novel focal adhesion kinase RAFTK in hematopoietic cells [J].
Avraham, S ;
Avraham, H .
LEUKEMIA & LYMPHOMA, 1997, 27 (3-4) :247-256
[9]   Modulation of T-cell activation by the glucocorticoid-induced leucine zipper factor via inhibition of nuclear factor κB [J].
Ayroldi, E ;
Migliorati, G ;
Bruscoli, S ;
Marchetti, C ;
Zollo, O ;
Cannarile, L ;
D'Adamio, F ;
Riccardi, C .
BLOOD, 2001, 98 (03) :743-753
[10]   ROLE OF INTERLEUKIN-6 IN THE GROWTH OF MYELOMA-DERIVED CELL-LINES [J].
BARUT, BA ;
ZON, LI ;
COCHRAN, MK ;
PAUL, SR ;
CHAUHAN, D ;
MOHRBACHER, A ;
FINGEROTH, J ;
ANDERSON, KC .
LEUKEMIA RESEARCH, 1992, 16 (10) :951-959