Altered Microenvironmental Regulation of Leukemic and Normal Stem Cells in Chronic Myelogenous Leukemia

被引:296
|
作者
Zhang, Bin [1 ]
Ho, Yin Wei [1 ]
Huang, Qin [2 ]
Maeda, Takahiro [1 ]
Lin, Allen [1 ]
Lee, Sung-uk [1 ]
Hair, Alan [3 ]
Holyoake, Tessa L. [3 ]
Huettner, Claudia [4 ]
Bhatia, Ravi [1 ]
机构
[1] City Hope Natl Med Ctr, Div Hematopoiet Stem Cell & Leukemia Res, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Dept Pathol, Duarte, CA 91010 USA
[3] Univ Glasgow, Inst Canc Sci, Coll Med Vet & Life Sci, Glasgow G61 1BD, Lanark, Scotland
[4] Dana Farber Canc Inst, Beffer Inst Appl Canc Sci, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
CHRONIC MYELOID-LEUKEMIA; BONE-MARROW; HEMATOPOIETIC STEM; MULTIPOTENT PROGENITORS; MALIGNANT PROGENITORS; NOD/SCID MICE; CHRONIC-PHASE; IN-VITRO; IMATINIB; CML;
D O I
10.1016/j.ccr.2012.02.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We characterized leukemia stem cells (LSC) in chronic phase chronic myelogenous leukemia (CML) using a transgenic mouse model. LSC were restricted to cells with long-term hematopoietic stem cell (LTHSC) phenotype. CML LTHSC demonstrated reduced homing and retention in the bone marrow (BM), related to decreased CXCL12 expression in CML BM, resulting from increased G-CSF production by leukemia cells. Altered cytokine expression in CML BM was associated with selective impairment of normal LTHSC growth and a growth advantage to CML LTHSC. Imatinib (IM) treatment partially corrected abnormalities in cytokine levels and LTHSC growth. These results were validated using human CML samples and provide improved understanding of microenvironmental regulation of normal and leukemic LTHSC and their response to IM in CML.
引用
收藏
页码:577 / 592
页数:16
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