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

被引:330
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 [肿瘤学];
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
相关论文
共 43 条
[1]
Long-term haematopoietic reconstitution by Trp53-/-p16Ink4a-/-p19Arf-/- multipotent progenitors [J].
Akala, Omobolaji O. ;
Park, In-Kyung ;
Qian, Dalong ;
Pihalja, Michael ;
Becker, Michael W. ;
Clarke, Michael F. .
NATURE, 2008, 453 (7192) :228-U12
[2]
A clonogenic common myeloid progenitor that gives rise to all myeloid lineages [J].
Akashi, K ;
Traver, D ;
Miyamoto, T ;
Weissman, IL .
NATURE, 2000, 404 (6774) :193-197
[3]
ABNORMAL FUNCTION OF THE BONE-MARROW MICROENVIRONMENT IN CHRONIC MYELOGENOUS LEUKEMIA - ROLE OF MALIGNANT STROMAL MACROPHAGES [J].
BHATIA, R ;
MCGLAVE, PB ;
DEWALD, GW ;
BLAZAR, BR ;
VERFAILLIE, CM .
BLOOD, 1995, 85 (12) :3636-3645
[4]
Hierarchy of molecular-pathway usage in bone marrow homing and its shift by cytokines [J].
Bonig, H ;
Priestley, GV ;
Papayannopoulou, T .
BLOOD, 2006, 107 (01) :79-86
[5]
Cappella P., 2008, CURR PROTOC CYTOM
[6]
Stromal-derived factor 1 inhibits the cycling of very primitive human hematopoietic cells in vitro and in NOD/SCID mice [J].
Cashman, J ;
Clark-Lewis, I ;
Eaves, A ;
Eaves, C .
BLOOD, 2002, 99 (03) :792-799
[7]
MCP-1, not MIP-1α, is the endogenous chemokine that cooperates with TGF-β to inhibit the cycling of primitive normal but not leukemic (CML) progenitors in long-term human marrow cultures [J].
Cashman, JD ;
Eaves, CJ ;
Sarris, AH ;
Eaves, AC .
BLOOD, 1998, 92 (07) :2338-2344
[8]
The Effect of CXCL12 Processing on CD34+ Cell Migration in Myeloproliferative Neoplasms [J].
Cho, Sool Yeon ;
Xu, Mingjiang ;
Roboz, John ;
Lu, Min ;
Mascarenhas, John ;
Hoffman, Ronald .
CANCER RESEARCH, 2010, 70 (08) :3402-3410
[9]
Leukemic stem cell persistence in chronic myeloid leukemia patients with sustained undetectable molecular residual disease [J].
Chomel, Jean-Claude ;
Bonnet, Marie-Laure ;
Sorel, Nathalie ;
Bertrand, Angelina ;
Meunier, Marie-Claude ;
Fichelson, Serge ;
Melkus, Michael ;
Bennaceur-Griscelli, Annelise ;
Guilhot, Francois ;
Turhan, Ali G. .
BLOOD, 2011, 118 (13) :3657-3660
[10]
Human chronic myeloid leukemia stem cells are insensitive to imatinib despite inhibition of BCR-ABL activity [J].
Corbin, Amie S. ;
Agarwal, Anupriya ;
Loriaux, Marc ;
Cortes, Jorge ;
Deininger, Michael W. ;
Druker, Brian J. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (01) :396-409