Proteomic analysis of hematopoietic stem cell-like fractions in leukemic disorders

被引:42
作者
Ota, J
Yamashita, Y
Okawa, K
Kisanuki, H
Fujiwara, S
Ishikawa, M
Choi, YL
Ueno, S
Ohki, R
Koinuma, K
Wada, T
Compton, D
Kadoya, T
Mano, H
机构
[1] Jichi Med Sch, Div Funct Genom, Tochigi 3290498, Japan
[2] Kirin Brewery Co Ltd, Div Pharmaceut, Pharmaceut Res Labs, Takasaki, Gumma 3701925, Japan
[3] Jichi Med Sch, Div Hematol, Tochigi 3290498, Japan
[4] Jichi Med Sch, Div Cardiol, Tochigi 3290498, Japan
[5] Jichi Med Sch, Dept Surg, Tochigi 3290498, Japan
[6] Jichi Med Sch, Dept Gynecol, Tochigi 3290498, Japan
[7] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Biochem, Hanover, NH 03755 USA
[8] Kirin Brewery Co Ltd, Div Pharmaceut, Prod Dept, R&D Ctr, Maebashi, Gumma 3710853, Japan
关键词
acute myeloid leukemia; proteome; AC133; NuMA;
D O I
10.1038/sj.onc.1206855
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA microarray analysis has been applied to identify molecular markers of human hematological malignancies. However, the relatively low correlation between the abundance of a given mRNA and that of the encoded protein makes it important to characterize the protein profile directly, or 'proteome,' of malignant cells in addition to the 'transcriptome.' To identify proteins specifically expressed in leukemias, here we isolated AC133(+) hematopoietic stem cell-like fractions from the bone marrow of 13 individuals with various leukemic disorders, and compared their protein profiles by two-dimensional electrophoresis. A total of 11 differentially expressed protein spots corresponding to 10 independent proteins were detected, and peptide fingerprinting combined with mass spectrometry of these proteins revealed them to include NuMA (nuclear protein that associates with the mitotic apparatus), heat shock proteins, and redox regulators. The abundance of NuMA in the leukemic blasts was significantly related to the presence of complex karyotype anomalies. Conditional expression of NuMA in a mouse myeloid cell line resulted in the induction of aneuploidy, cell cycle arrest in G(2)-M phases, and apoptosis. These results demonstrate the potential of proteome analysis with background-matched cell fractions obtained from fresh clinical specimens to provide insight into the mechanism of human leukemogenesis.
引用
收藏
页码:5720 / 5728
页数:9
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