The role of ZAP70 kinase in acute lymphoblastic leukemia infiltration into the central nervous system

被引:53
作者
Alsadeq, Ameera [1 ,2 ]
Fedders, Henning [1 ,2 ]
Vokuhl, Christian [2 ,3 ]
Belau, Nele M. [1 ,2 ]
Zimmermann, Martin [4 ]
Wirbelauer, Tim [1 ,2 ]
Spielberg, Steffi [1 ,2 ]
Vossen-Gajcy, Michaela [1 ,2 ]
Cario, Gunnar [1 ,2 ]
Schrappe, Martin [1 ,2 ]
Schewe, Denis M. [1 ,2 ]
机构
[1] Christian Albrechts Univ Kiel, Dept Gen Pediat, ALL BFM Study Grp, Kiel, Germany
[2] Univ Med Ctr Schleswig Holstein, Kiel, Germany
[3] Univ Med Ctr Schleswig Holstein, Kiel Pediat Tumor Registry, Dept Pediat Pathol, Kiel, Germany
[4] Hannover Med Sch, Pediat Hematol & Oncol, Hannover, Germany
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; TRAUMATIC LUMBAR PUNCTURE; TYROSINE KINASE; CHILDHOOD LEUKEMIA; CNS INFILTRATION; CELL LEUKEMIA; LATE RELAPSES; ZAP-70; EXPRESSION; MIGRATION;
D O I
10.3324/haematol.2016.147744
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central nervous system infiltration and relapse are poorly understood in childhood acute lymphoblastic leukemia. We examined the role of zeta-chain-associated protein kinase 70 in preclinical models of central nervous system leukemia and performed correlative studies in patients. Zeta-chain-associated protein kinase 70 expression in acute lymphoblastic leukemia cells was modulated using short hairpin ribonucleic acid-mediated knockdown or ectopic expression. We show that zeta-chain-associated protein kinase 70 regulates CCR7/CXCR4 via activation of extracellular signal-regulated kinases. High expression of zeta-chain-associated protein kinase 70 in acute lymphoblastic leukemia cells resulted in a higher proportion of central nervous system leukemia in xenografts as compared to zeta-chain-associated protein kinase 70 low expressing counterparts. High zeta-chain-associated protein kinase 70 also enhanced the migration potential towards CCL19/CXCL12 gradients in vitro. CCR7 blockade almost abrogated homing of acute lymphoblastic leukemia cells to the central nervous system in xenografts. In 130 B-cell precursor acute lymphoblastic leukemia and 117 T-cell acute lymphoblastic leukemia patients, zeta-chain-associated protein kinase 70 and CCR7/CXCR4 expression levels were significantly correlated. Zetachain- associated protein kinase 70 expression correlated with central nervous system disease in B-cell precursor acute lymphoblastic leukemia, and CCR7/CXCR4 correlated with central nervous system involvement in T-cell acute lymphoblastic leukemia patients. In multivariate analysis, zeta-chain-associated protein kinase 70 expression levels in the upper third and fourth quartiles were associated with central nervous system involvement in B-cell precursor acute lymphoblastic leukemia (odds ratio=7.48, 95% confidence interval, 2.06-27.17; odds ratio=6.86, 95% confidence interval, 1.86-25.26, respectively). CCR7 expression in the upper fourth quartile correlated with central nervous system positivity in T-cell acute lymphoblastic leukemia (odds ratio=11.00, 95% confidence interval, 2.00-60.62). We propose zeta-chain-associated protein kinase 70, CCR7 and CXCR4 as markers of central nervous system infiltration in acute lymphoblastic leukemia warranting prospective investigation.
引用
收藏
页码:346 / 355
页数:10
相关论文
共 51 条
[1]   Chronic lymphocytic leukemia presenting with symptomatic central nervous system involvement [J].
Akintola-Ogunremi, O ;
Whitney, C ;
Mathur, SC ;
Finch, CN .
ANNALS OF HEMATOLOGY, 2002, 81 (07) :402-404
[2]   Anti-CCR7 monoclonal antibodies as a novel tool for the treatment of chronic lymphocyte leukemia [J].
Alfonso-Perez, Manuel ;
Lopez-Giral, Sonia ;
Quintana, Nuria E. ;
Loscertales, Javier ;
Martin-Jimenez, Patricia ;
Munoz, Cecilia .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 79 (06) :1157-1165
[3]   Effects of p38α/β inhibition on acute lymphoblastic leukemia proliferation and survival in vivo [J].
Alsadeq, A. ;
Strube, S. ;
Krause, S. ;
Carlet, M. ;
Jeremias, I. ;
Vokuhl, C. ;
Loges, S. ;
Aguirre-Ghiso, J. A. ;
Trauzold, A. ;
Cario, G. ;
Stanulla, M. ;
Schrappe, M. ;
Schewe, D. M. .
LEUKEMIA, 2015, 29 (12) :2307-2316
[4]   The structure, regulation, and function of ZAP-70 [J].
Au-Yeung, Byron B. ;
Deindl, Sebastian ;
Hsu, Lih-Yun ;
Palacios, Emil H. ;
Levin, Susan E. ;
Kuriyan, John ;
Weiss, Arthur .
IMMUNOLOGICAL REVIEWS, 2009, 228 :41-57
[5]   CCR7 signalling as an essential regulator of CNS infiltration in T-cell leukaemia [J].
Buonamici, Silvia ;
Trimarchi, Thomas ;
Ruocco, Maria Grazia ;
Reavie, Linsey ;
Cathelin, Severine ;
Mar, Brenton G. ;
Klinakis, Apostolos ;
Lukyanov, Yevgeniy ;
Tseng, Jen-Chieh ;
Sen, Filiz ;
Gehrie, Eric ;
Li, Mengling ;
Newcomb, Elizabeth ;
Zavadil, Jiri ;
Meruelo, Daniel ;
Lipp, Martin ;
Ibrahim, Sherif ;
Efstratiadis, Argiris ;
Zagzag, David ;
Bromberg, Jonathan S. ;
Dustin, Michael L. ;
Aifantis, Iannis .
NATURE, 2009, 459 (7249) :1000-U129
[6]   Diagnostic cerebrospinal fluid examination in children with acute lymphoblastic leukemia:: Significance of low leukocyte counts with blasts or traumatic lumbar puncture [J].
Bürger, B ;
Zimmermann, M ;
Mann, G ;
Kühl, J ;
Löning, L ;
Reihm, H ;
Reiter, A ;
Schrappe, M .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (02) :184-188
[7]   ZAP-70 Promotes the Infiltration of Malignant B-Lymphocytes into the Bone Marrow by Enhancing Signaling and Migration after CXCR4 Stimulation [J].
Calpe, Eva ;
Purroy, Noelia ;
Carpio, Cecilia ;
Abrisqueta, Pau ;
Carabia, Julia ;
Palacio, Carles ;
Castellvi, Josep ;
Crespo, Marta ;
Bosch, Francesc .
PLOS ONE, 2013, 8 (12)
[8]   ZAP-70 enhances migration of malignant B lymphocytes toward CCL21 by inducing CCR7 expression via IgM-ERK1/2 activation [J].
Calpe, Eva ;
Codony, Carles ;
Joao Baptista, Maria ;
Abrisqueta, Pau ;
Carpio, Cecilia ;
Purroy, Noelia ;
Bosch, Francesc ;
Crespo, Marta .
BLOOD, 2011, 118 (16) :4401-4410
[9]   Analysis of ZAP70 expression in adult acute lymphoblastic leukaemia by real time quantitative PCR [J].
Chakupurakal, Geothy ;
Bell, Andrew ;
Griffiths, Mike ;
Wandroo, Farooq ;
Moss, Paul .
MOLECULAR CYTOGENETICS, 2012, 5
[10]   ZAP-70 directly enhances TgM signaling in chronic lymphocytic leukemia [J].
Chen, LG ;
Apgar, J ;
Huynh, L ;
Dicker, F ;
Giago-McGahan, T ;
Rassenti, L ;
Weiss, A ;
Kipps, TJ .
BLOOD, 2005, 105 (05) :2036-2041