Gene expression profiles of CD34+ cells in myelodysplastic syndromes:: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype

被引:165
作者
Pellagatti, Andrea
Cazzola, Mario
Giagounidis, Aristoteles A. N.
Malcovati, Luca
Della Porta, Matteo G.
Killick, Sally
Campbell, Lisa J.
Wang, Li
Langford, Cordelia F.
Fidler, Carrie
Oscier, David
Aul, Carlo
Wainscoat, James S.
Boultwood, Jacqueline [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, LRF Mol Haematol Unit, Oxford OX3 9DU, England
[2] Univ Pavia, Sch Med, Div Hematol, IRCCS,Policlin S Matteo, Pavia, Italy
[3] St Johannes Hosp, Med Klin 2, Duisburg, Germany
[4] Royal Bournemouth Hosp, Dept Haematol, Bournemouth, Dorset, England
[5] Sanger Inst, Microarray Facil, Cambridge, England
关键词
D O I
10.1182/blood-2005-12-4769
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To gain insight into the poorly understood pathophysiology of the myelodysplastic syndromes (MDSs), we have determined the gene expression profiles of the CD34(+) cells of 55 patients with MDS by using a comprehensive array platform. These profiles showed many similarities to reported interferon-gamma-induced gene expression in normal CD34(+) cells; indeed the 2 most up-regulated genes, IFIT1 and IFITM1, are interferon-stimulated genes (ISGs). Alterations in the expression of ISGs may play a role in the hematologic features of MDS, such as peripheral blood cytopenias. Up-regulation of IFIT1 is a potential diagnostic marker for MDS. We determined whether distinct gene expression profiles were associated with specific FAB and cytogenetic groups. CD34(+) cells from patients with refractory anemia with ringed sideroblasts (RARS) showed a particular gene expression profile characterized by up-regulation of mitochondrial-related genes and, in particular, of those of heme synthesis (eg, ALAS2). CD34(+) cells from patients with the del(5q) had a distinct gene expression profile, characterized by down-regulation of genes assigned to 5q, and up-regulation of the histone HIST1 gene cluster at chromosome 6p21 and of genes related to the actin cytoskeleton. This study provides important and new insights into the pathophysiology of MDS.
引用
收藏
页码:337 / 345
页数:9
相关论文
共 56 条
[1]   MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia [J].
Armstrong, SA ;
Staunton, JE ;
Silverman, LB ;
Pieters, R ;
de Boer, ML ;
Minden, MD ;
Sallan, SE ;
Lander, ES ;
Golub, TR ;
Korsmeyer, SJ .
NATURE GENETICS, 2002, 30 (01) :41-47
[2]  
Aul C, 1998, HAEMATOLOGICA, V83, P71
[3]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[4]  
BENNETT JM, 1982, BRIT J HAEMATOL, V51, P189, DOI 10.1111/j.1365-2141.1982.tb08475.x
[5]   Low expression of the putative tumour suppressor gene gravin in chronic myeloid leukaemia, myelodysplastic syndromes and acute myeloid leukaemia [J].
Boultwood, J ;
Pellagatti, A ;
Watkins, F ;
Campbell, LJ ;
Esoof, N ;
Cross, NCP ;
Eagleton, H ;
Littlewood, TJ ;
Fidler, C ;
Wainscoat, JS .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 126 (04) :508-511
[6]  
BOULTWOOD J, 1994, BLOOD, V84, P3253
[7]   Fas/Apo-1(CD95) expression and apoptosis in patients with myelodysplastic syndromes [J].
Bouscary, D ;
DeVos, J ;
Guesnu, M ;
Jondeau, K ;
Viguier, F ;
Melle, J ;
Picard, F ;
Dreyfus, F ;
FontenayRoupie, M .
LEUKEMIA, 1997, 11 (06) :839-845
[8]   Use of gene-expression profiling to identify prognostic subclasses in adult acute myeloid leukemia [J].
Bullinger, L ;
Döhner, K ;
Bair, E ;
Fröhling, S ;
Schlenk, RF ;
Tibshirani, R ;
Döhner, H ;
Pollack, JR .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (16) :1605-1616
[9]   Mitochondrial ferritin expression in erythroid cells from patients with sideroblastic anemia [J].
Cazzola, M ;
Invernizzi, R ;
Bergamaschi, G ;
Levi, S ;
Corsi, B ;
Travaglino, E ;
Rolandi, V ;
Biasiotto, G ;
Drysdale, J ;
Arosio, P .
BLOOD, 2003, 101 (05) :1996-2000
[10]   Stem cell factor increases the expression of FLIP that inhibits IFNγ-induced apoptosis in human erythroid progenitor cells [J].
Chung, IJ ;
Dai, CH ;
Krantz, SB .
BLOOD, 2003, 101 (04) :1324-1328