ADAM8 Is an Antigen of Tyrosine Kinase Inhibitor-Resistant Chronic Myeloid Leukemia Cells Identified by Patient-Derived Induced Pluripotent Stem Cells

被引:33
|
作者
Miyauchi, Masashi [1 ]
Koya, Junji [1 ]
Arai, Shunya [1 ]
Yamazaki, Sho [1 ]
Honda, Akira [1 ]
Kataoka, Keisuke [1 ]
Yoshimi, Akihide [1 ]
Taoka, Kazuki [1 ]
Kumano, Keiki [1 ]
Kurokawa, Mineo [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138655, Japan
来源
STEM CELL REPORTS | 2018年 / 10卷 / 03期
基金
日本学术振兴会;
关键词
CHRONIC MYELOGENOUS LEUKEMIA; BLAST CRISIS; E-SELECTIN; PHILADELPHIA-CHROMOSOME; IN-VITRO; EXPRESSION; IMATINIB; BCR/ABL; CANCER; CML;
D O I
10.1016/j.stemcr.2018.01.015
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Properties of cancer stem cells involved in drug resistance and relapse have significant effects on clinical outcome. Although tyrosine kinase inhibitors (TKIs) have dramatically improved survival of patients with chronic myeloid leukemia (CML), TKIs have not fully cured CMLdue to TKI-resistantCMLstem cells. Moreover, relapse after discontinuation of TKIs has not been predicted inCMLpatients with the best TKI response. In our study, a model of CML stem cells derived from CML induced pluripotent stem cells identified ADAM8 as an antigen of TKI-resistant CML cells. The inhibition of expression or metalloproteinase activity of ADAM8 restored TKI sensitivity in primary samples. In addition, residual CML cells in patients with optimal TKI response were concentrated in the ADAM8+ population. Our study demonstrates that ADAM8 is a marker of residual CML cells even in patients with optimal TKI response and would be a predictor of relapse and a therapeutic target of TKI-resistant CML cells.
引用
收藏
页码:1115 / 1130
页数:16
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