Mechanisms underlying therapeutic resistance of tyrosine kinase inhibitors in chronic myeloid leukemia

被引:16
作者
Sun, Jingnan [1 ]
Hu, Ruiping [1 ]
Han, Mengyuan [1 ]
Tan, Yehui [1 ]
Xie, Mengqing [1 ,3 ]
Gao, Sujun [1 ]
Hu, Ji-Fan [1 ,2 ,4 ]
机构
[1] First Hosp Jilin Univ, Hematol Dept, Changchun 130021, Jilin, Peoples R China
[2] Stanford Univ, Palo Alto Vet Inst Res, Med Sch, Palo Alto, CA 94304 USA
[3] Chinese Acad Med Sci, Oncol Dept, Canc Hosp, Langfang 065001, Peoples R China
[4] Palo Alto Vet Inst Res, Palo Alto, CA 94304 USA
基金
中国国家自然科学基金;
关键词
chronic myeloid leukemia; TKI Resistance; ABL mutation; mechanism; BCR-ABL1; IMATINIB; CML; IDENTIFICATION; STAT5;
D O I
10.7150/ijbs.86305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic myeloid leukemia (CML) is a malignant clonal disease involving hematopoietic stem cells that is characterized by myeloid cell proliferation in bone marrow and peripheral blood, and the presence of the Philadelphia (Ph) chromosome with BCR-ABL fusion gene. Treatment of CML has dramatically improved since the advent of tyrosine kinase inhibitors (TKI). However, there are a small subset of CML patients who develop resistance to TKI. Mutations in the ABL kinase domain (KD) are currently recognized as the leading cause of TKI resistance in CML. In this review, we discuss the concept of resistance and summarize recent advances exploring the mechanisms underlying CML resistance. Overcoming TKI resistance appears to be the most successful approach to reduce the burden of leukemia and enhance cures for CML. Advances in new strategies to combat drug resistance may rapidly change the management of TKI-resistant CML and expand the prospects for available therapies.
引用
收藏
页码:175 / 181
页数:7
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