IL-6 Controls Leukemic Multipotent Progenitor Cell Fate and Contributes to Chronic Myelogenous Leukemia Development

被引:280
作者
Reynaud, Damien [1 ,2 ]
Pietras, Eric [1 ,2 ]
Barry-Holson, Keegan [1 ,2 ]
Mir, Alain [3 ]
Binnewies, Mikhail [1 ,2 ]
Jeanne, Marion [1 ,2 ]
Sala-Torra, Olga [4 ]
Radich, Jerald P. [4 ]
Passegue, Emmanuelle [1 ,2 ]
机构
[1] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, Div Hematol Oncol, San Francisco, CA 94143 USA
[3] Fluidigm Corp, San Francisco, CA 94080 USA
[4] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
关键词
CHRONIC MYELOID-LEUKEMIA; COLONY-STIMULATING FACTOR; HEMATOPOIETIC STEM-CELLS; BCR-ABL; MYELOPROLIFERATIVE DISEASE; LYMPHOBLASTIC-LEUKEMIA; IMATINIB; QUIESCENT; MICE; DIFFERENTIATION;
D O I
10.1016/j.ccr.2011.10.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using a mouse model recapitulating the main features of human chronic myelogenous leukemia (CML), we uncover the hierarchy of leukemic stem and progenitor cells contributing to disease pathogenesis. We refine the characterization of CML leukemic stem cells (LSCs) to the most immature long-term hematopoietic stem cells (LT-HSCs) and identify some important molecular deregulations underlying their aberrant behavior. We find that CML multipotent progenitors (MPPs) exhibit an aberrant B-lymphoid potential but are redirected toward the myeloid lineage by the action of the proinflammatory cytokine IL-6. We show that BCR/ABL activity controls II-6 expression thereby establishing a paracrine feedback loop that sustains CML development. These results describe how proinflammatory tumor environment affects leukemic progenitor cell fate and contributes to CML pathogenesis.
引用
收藏
页码:661 / 673
页数:13
相关论文
共 34 条
[1]  
Anand M, 1998, HEMATOL ONCOL, V16, P143
[2]   Modeling the initiation and progression of human acute leukemia in mice [J].
Barabe, Frederic ;
Kennedy, James A. ;
Hope, Kristin J. ;
Dick, John E. .
SCIENCE, 2007, 316 (5824) :600-604
[3]   Primitive, quiescent and difficult to kill - The role of non-proliferating stem cells in chronic myeloid leukemia [J].
Barnes, David J. ;
Melo, Junia V. .
CELL CYCLE, 2006, 5 (24) :2862-2866
[4]   Intermediate-Term Hematopoietic Stem Cells with Extended but Time-Limited Reconstitution Potential [J].
Benveniste, Patricia ;
Frelin, Catherine ;
Janmohamed, Salima ;
Barbara, Mary ;
Herrington, Robert ;
Hyam, Deborah ;
Iscove, Norman N. .
CELL STEM CELL, 2010, 6 (01) :48-58
[5]   Marrow fibrosis and its relevance during imatinib treatment of chronic myeloid leukemia [J].
Buesche, G. ;
Ganser, A. ;
Schlegelberger, B. ;
von Neuhoff, N. ;
Gadzicki, D. ;
Hecker, H. ;
Bock, O. ;
Frye, B. ;
Kreipe, H. .
LEUKEMIA, 2007, 21 (12) :2420-2427
[6]   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
[7]   BCL6 enables Ph+ acute lymphoblastic leukaemia cells to survive BCR-ABL1 kinase inhibition [J].
Duy, Cihangir ;
Hurtz, Christian ;
Shojaee, Seyedmehdi ;
Cerchietti, Leandro ;
Geng, Huimin ;
Swaminathan, Srividya ;
Klemm, Lars ;
Kweon, Soo-mi ;
Nahar, Rahul ;
Braig, Melanie ;
Park, Eugene ;
Kim, Yong-mi ;
Hofmann, Wolf-Karsten ;
Herzog, Sebastian ;
Jumaa, Hassan ;
Koeffler, H. Phillip ;
Yu, J. Jessica ;
Heisterkamp, Nora ;
Graeber, Thomas G. ;
Wu, Hong ;
Ye, B. Hilda ;
Melnick, Ari ;
Mueschen, Markus .
NATURE, 2011, 473 (7347) :384-U572
[8]   Isolation of a highly quiescent subpopulation of primitive leukemic cells in chronic myeloid leukemia [J].
Holyoake, T ;
Jiang, XY ;
Eaves, C ;
Eaves, A .
BLOOD, 1999, 94 (06) :2056-2064
[9]   Interleukin-6 and its receptor in cancer - Implications for translational therapeutics [J].
Hong, David S. ;
Angelo, Laura S. ;
Kurzrock, Razelle .
CANCER, 2007, 110 (09) :1911-1928
[10]   Targeting multiple kinase pathways in leukemic progenitors and stem cells is essential for improved treatment of Ph+ leukemia in mice [J].
Hu, Yiguo ;
Swerdlow, Sarah ;
Duffy, Theodore M. ;
Weinmann, Roberto ;
Lee, Francis Y. ;
Li, Shaoguang .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (45) :16870-16875