Stem-like tumor cells confer drug resistant properties to mantle cell lymphoma

被引:21
作者
Jung, Hyun Joo [1 ,2 ]
Chen, Zheng [1 ]
McCarty, Nami [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Ctr Stem Cell Res, Brown Fdn, Inst Mol Med Prevent Human Dis IMM, Houston, TX 77030 USA
[2] Ajou Univ, Sch Med, Dept Pediat, Div Hematol Oncol, Suwon 441749, South Korea
关键词
Mantle cell lymphoma; chemotherapy resistance; cancer stem cells; cancer-initiating cells; non-Hodgkin lymphoma; IN-VITRO; COMBINATION CHEMOTHERAPY; LEUKEMIA; RITUXIMAB; GLYCOPROTEIN; SENSITIVITY; MANAGEMENT; APOPTOSIS; THERAPY; BIOLOGY;
D O I
10.3109/10428194.2011.562570
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
We recently identified clonogenic malignant stem cell populations in human mantle cell lymphoma (MCL), a particularly deadly subtype of non-Hodgkin lymphoma (NHL). We discovered that CD45+CD19- MCL cells, which we termed MCL-initiating cells (MCL-ICs), are highly tumorigenic and display self-renewal capacity in vivo; in contrast, CD45+CD19+ MCL cells, which constitute the vast majority of cells within the tumors, show no self-renewal capacity and greatly reduced tumorigenicity. Given the newly appreciated role of cancer-initiating cells in the drug resistance of cancers, it is critical to investigate whether CD45+CD19- MCL-ICs play a role in the drug resistance of human MCL. We discovered that MCL-ICs were more resistant to clinically relevant chemotherapeutic agents, in combination or in a single regimen, compared to CD45+CD19+ cells, and that this drug resistance was largely due to quiescent properties with enriched ABC transporters. In conclusion, designing novel therapies to kill CD45+CD19- MCL-ICs may prevent relapse and increase patient survival.
引用
收藏
页码:1066 / 1079
页数:14
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