Leukemia stem cells: the root of chronic myeloid leukemia.
10.1007/s13238-015-0143-7
- Author:
Hong ZHOU
1
;
Rongzhen XU
Author Information
1. Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education, Department of Hematology, Zhejiang University, Hangzhou, 310009, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Chemokines;
metabolism;
Epigenesis, Genetic;
Humans;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive;
genetics;
metabolism;
pathology;
Neoplastic Stem Cells;
metabolism;
pathology;
Transcription Factors;
metabolism;
Tumor Microenvironment
- From:
Protein & Cell
2015;6(6):403-412
- CountryChina
- Language:English
-
Abstract:
Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder characterized by a chromosome translocation that generates the Bcr-Abl oncogene encoding a constitutive kinase activity. Despite remarkable success in controlling CML at chronic phase by Bcr-Abl tyrosine kinase inhibitors (TKIs), a significant proportion of CML patients treated with TKIs develop drug resistance due to the inability of TKIs to kill leukemia stem cells (LSCs) that are responsible for initiation, drug resistance, and relapse of CML. Therefore, there is an urgent need for more potent and safer therapies against leukemia stem cells for curing CML. A number of LSC-associated targets and corresponding signaling pathways, including CaMKII-γ, a critical molecular switch for co-activating multiple LSC-associated signaling pathways, have been identified over the past decades and various small inhibitors targeting LSC are also under development. Increasing evidence shows that leukemia stem cells are the root of CML and targeting LSC may offer a curable treatment option for CML patients. This review summarizes the molecular biology of LSC and its-associated targets, and the potential clinical application in chronic myeloid leukemia.
