The CXCR4 chemokine receptor in acute and chronic leukaemia:: a marrow homing receptor and potential therapeutic target

被引:133
作者
Burger, Jan A.
Buerkle, Andrea
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Unit 428, Houston, TX 77230 USA
[2] Freiburg Univ Hosp, Dept Med, Div Haematol Oncol, Freiburg, Germany
关键词
CXCR4 chemokine receptor; CXCL12; leukaemia; leukaemia microenvironment; CXCR4; antagonists;
D O I
10.1111/j.1365-2141.2007.06590.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chemokine (C-X-C motif) receptor 4 (CXCR4) is essential for homing and maintenance of haematopoietic stem cells in distinct stromal cell niches within the marrow. Chemotactic responsiveness of haematopoietic stem cells is restricted to the ligand for CXCR4, stromal cell-derived factor-1 (SDF-1/CXCL12), which is constitutively secreted by marrow stromal cells. Myeloid and lymphoid leukaemia cells also express CXCR4 that induces leukaemia cell chemotaxis and migration beneath marrow stromal cells. CXCR4 expression levels have a major prognostic impact in acute myeloid leukaemia. There is growing in vitro and in vivo evidence that CXCR4 expression by leukaemia cells allows for homing and their retention within the marrow. As such, leukaemia cells appear to utilise CXCR4 to access niches that are normally restricted to progenitor cells, and thereby reside in a microenvironment that favours their growth and survival. CXCR4- and integrin-mediated contact between leukaemia cells and stromal cells protects leukaemia cells from spontaneous and chemotherapy-induced cell death and therefore may represent a mechanism to explain minimal residual disease and subsequent relapses commonly seen in the treatment of these diseases. This review summarises our current knowledge regarding the importance of CXCR4 in acute and chronic leukaemia, discusses the importance of CXCR4 detection by flow cytometry in the diagnostic workup of leukaemia patients, and introduces the potential role of CXCR4-targeting compounds for the treatment of leukaemia patients.
引用
收藏
页码:288 / 296
页数:9
相关论文
共 94 条
[1]   The chemokine SDF-1 is a chemoattractant for human CD34(+) hematopoietic progenitor cells and provides a new mechanism to explain the mobilization of CD34(+) progenitors to peripheral blood [J].
Aiuti, A ;
Webb, IJ ;
Bleul, C ;
Springer, T ;
GutierrezRamos, JC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) :111-120
[2]  
Andreeff M., 2006, BLOOD, V108
[3]   The chemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes [J].
Balabanian, K ;
Lagane, B ;
Infantino, S ;
Chow, KYC ;
Harriague, J ;
Moepps, B ;
Arenzana-Seisdedos, F ;
Thelen, M ;
Bachelerie, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (42) :35760-35766
[4]   CXCR4 and SDF-1 expression in B-cell chronic lymphocytic leukemia and stage of the disease [J].
Barretina, J ;
Juncà, J ;
Llano, A ;
Gutiérrez, A ;
Flores, A ;
Blanco, J ;
Clotet, B ;
Esté, JA .
ANNALS OF HEMATOLOGY, 2003, 82 (08) :500-505
[5]   Defective p38 mitogen-activated protein kinase signaling impairs chemotaxic but not proliferative responses to stromal-derived factor-1α in acute lymphoblastic leukemia [J].
Bendall, LJ ;
Baraz, R ;
Juarez, J ;
Shen, W ;
Bradstock, KF .
CANCER RESEARCH, 2005, 65 (08) :3290-3298
[6]   The lymphocyte chemoattractant SDF-1 is a ligand for LESTR/fusin and blocks HIV-1 entry [J].
Bleul, CC ;
Farzan, M ;
Choe, H ;
Parolin, C ;
ClarkLewis, I ;
Sodroski, J ;
Springer, TA .
NATURE, 1996, 382 (6594) :829-833
[7]  
Bleul CC, 2000, EUR J IMMUNOL, V30, P3371, DOI 10.1002/1521-4141(2000012)30:12<3371::AID-IMMU3371>3.0.CO
[8]  
2-L
[9]   A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1) [J].
Bleul, CC ;
Fuhlbrigge, RC ;
Casasnovas, JM ;
Aiuti, A ;
Springer, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) :1101-1109
[10]   Effects of the chemokine stromal cell-derived factor-1 on the migration and localization of precursor-B acute lymphoblastic leukemia cells within bone marrow stromal layers [J].
Bradstock, KF ;
Makrynikola, V ;
Bianchi, A ;
Shen, W ;
Hewson, J ;
Gottlieb, DJ .
LEUKEMIA, 2000, 14 (05) :882-888