Bmi-1 determines the proliferative capacity of normal and leukaemic stem cells

被引:1159
作者
Lessard, J
Sauvageau, G
机构
[1] Clin Res Inst Montreal, Lab Mol Genet Hemopoiet Stem Cells, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Hosp Maisonneuve Rosemont, Dept Med, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Hosp Maisonneuve Rosemont, Div Hematol, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/nature01572
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
An emerging concept in the field of cancer biology is that a rare population of 'tumour stem cells' exists among the heterogeneous group of cells that constitute a tumour. This concept, best described with human leukaemia, indicates that stem cell function ( whether normal or neoplastic) might be defined by a common set of critical genes. Here we show that the Polycomb group gene Bmi-1 has a key role in regulating the proliferative activity of normal stem and progenitor cells. Most importantly, we provide evidence that the proliferative potential of leukaemic stem and progenitor cells lacking Bmi-1 is compromised because they eventually undergo proliferation arrest and show signs of differentiation and apoptosis, leading to transplant failure of the leukaemia. Complementation studies showed that Bmi-1 completely rescues these proliferative defects. These studies therefore indicate that Bmi-1 has an essential role in regulating the proliferative activity of both normal and leukaemic stem cells.
引用
收藏
页码:255 / 260
页数:6
相关论文
共 24 条
[1]  
Appelbaum F R, 2001, Hematology Am Soc Hematol Educ Program, P62
[2]   Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737
[3]   The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9 [J].
Borrow, J ;
Shearman, AM ;
Stanton, VP ;
Becher, R ;
Collins, T ;
Williams, AJ ;
Dube, I ;
Katz, F ;
Kwong, YL ;
Morris, C ;
Ohyashiki, K ;
Toyama, K ;
Rowley, J ;
Housman, DE .
NATURE GENETICS, 1996, 12 (02) :159-167
[4]  
BRADY G, 1990, Methods in Molecular and Cellular Biology, V2, P17
[5]  
Dimri GP, 2002, CANCER RES, V62, P4736
[6]   The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus [J].
Jacobs, JJL ;
Kieboom, K ;
Marino, S ;
DePinho, RA ;
van Lohuizen, M .
NATURE, 1999, 397 (6715) :164-168
[7]   The interleukin-3 receptor alpha chain is a unique marker for human acute myelogenous leukemia stem cells [J].
Jordan, CT ;
Upchurch, D ;
Szilvassy, SJ ;
Guzman, ML ;
Howard, DS ;
Pettigrew, AL ;
Meyerrose, T ;
Rossi, R ;
Grimes, B ;
Rizzieri, DA ;
Luger, SM ;
Phillips, GL .
LEUKEMIA, 2000, 14 (10) :1777-1784
[8]   Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2 [J].
Kamijo, T ;
Weber, JD ;
Zambetti, G ;
Zindy, F ;
Roussel, MF ;
Sherr, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8292-8297
[9]   Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b [J].
Kroon, E ;
Krosl, J ;
Thorsteinsdottir, U ;
Baban, S ;
Buchberg, AM ;
Sauvageau, G .
EMBO JOURNAL, 1998, 17 (13) :3714-3725
[10]   Cellular proliferation and transformation induced by HOXB4 and HOXB3 proteins involves cooperation with PBX1 [J].
Krosl, J ;
Baban, S ;
Krosl, G ;
Rozenfeld, S ;
Largman, C ;
Sauvageau, G .
ONCOGENE, 1998, 16 (26) :3403-3412