Bortezomib-resistant nuclear factor κB expression in stem-like cells in mantle cell lymphoma

被引:18
作者
Jung, Hyun Joo [1 ,2 ]
Chen, Zheng [1 ]
Fayad, Luis [3 ]
Wang, Michael [3 ]
Romaguera, Jorge [3 ]
Kwak, Larry W. [3 ]
McCarty, Nami [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Brown Fdn Inst Mol Med Prevent Human Dis, Ctr Stem Cell Res, Houston, TX 77030 USA
[2] Ajou Univ, Ajou Univ Hosp, Dept Pediat, Div Hematol Oncol,Sch Med, Suwon 441749, South Korea
[3] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
PROTEASOME INHIBITOR BORTEZOMIB; PHASE-II; LEUKEMIA; CANCER; ACTIVATION; INDUCTION;
D O I
10.1016/j.exphem.2011.10.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mantle cell lymphoma (MCL) is a subtype of B-cell Non-Hodgkin's Lymphoma (NHL) and accounts for approximately 6% of all lymphomas. Unlike small lymphocytic lymphoma and chronic lymphocytic lymphoma, which are relatively sensitive to chemotherapy, MCL is highly refractory to most chemotherapy, and has the worst survival rate among NHL patients. Stem-like cells in MCL, which we have termed mantle cell lymphoma-initiating cells (MCL-ICs), enriched in the population that are lack of prototypic B-cell marker CD19. These cells were able to self-renew upon serial transplantation and are highly tumorigenic. Importantly, these stem-like cells confer chemotherapeutic resistance to MCL. In this report, we show that stem-like MCL-ICs are resistant to bortezomib, as well as chemotherapeutic regimens containing bortezomib, despite constitutive nuclear factor-kappa B (NF-kappa B) expression. Interestingly, bortezomib treatment induced MCL-IC differentiation in plasma-like cells with upregulated expression of CD38 and CD138. This process was accompanied by expression of plasma cell differentiation transcriptional factors, BLIMP-1 and IRF4. This article is the first to show that stem-like MCL cells utilize constitutive NF-kappa B expression for survival. Given that the NF-kappa B expression in MCL-ICs is resistant to bortezomib, it will be important to find alternative therapeutic strategies to inhibit NF-kappa B expression. (C) 2012 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc.
引用
收藏
页码:107 / 118
页数:12
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