Zhou Hong, Xu Rongzhen
Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education, Department of Hematology, Zhejiang University, Hangzhou, 310009, China.
Protein Cell. 2015 Jun;6(6):403-12. doi: 10.1007/s13238-015-0143-7. Epub 2015 Mar 10.
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.
慢性髓性白血病(CML)是一种克隆性骨髓增殖性疾病,其特征在于染色体易位,产生编码组成型激酶活性的Bcr-Abl癌基因。尽管通过Bcr-Abl酪氨酸激酶抑制剂(TKIs)在控制慢性期CML方面取得了显著成功,但相当一部分接受TKIs治疗的CML患者由于TKIs无法杀死导致CML起始、耐药和复发的白血病干细胞(LSCs)而产生耐药性。因此,迫切需要更有效、更安全的抗白血病干细胞疗法来治愈CML。在过去几十年中,已经确定了许多与LSC相关的靶点和相应的信号通路,包括CaMKII-γ,它是共同激活多个与LSC相关的信号通路的关键分子开关,并且各种靶向LSC的小分子抑制剂也在开发中。越来越多的证据表明,白血病干细胞是CML的根源,靶向LSC可能为CML患者提供可治愈的治疗选择。本综述总结了LSC及其相关靶点的分子生物学,以及在慢性髓性白血病中的潜在临床应用。