Kadia Tapan Mahendra, Kantarjian Hagop M, Konopleva Marina
The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Oncotarget. 2019 Feb 8;10(12):1250-1265. doi: 10.18632/oncotarget.26579.
Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, affecting approximately 21,000 people annually (nearly 11,000 deaths) in the United States. B-cell lymphoma 2 (BCL-2) family proteins, notably myeloid cell leukemia-1 (MCL-1), have been associated with both the development and persistence of AML. MCL-1 is one of the predominant BCL-2 family members expressed in samples from patients with untreated AML. MCL-1 is a critical cell survival factor for cancer and contributes to chemotherapy resistance by directly affecting cell death pathways. Here, we review the role of MCL-1 in AML and the mechanisms by which the potent cyclin-dependent kinase 9 inhibitor alvocidib, through regulation of MCL-1, may serve as a rational therapeutic approach against the disease.
急性髓系白血病(AML)是成人急性白血病最常见的形式,在美国每年影响约21000人(近11000人死亡)。B细胞淋巴瘤2(BCL-2)家族蛋白,尤其是髓系细胞白血病-1(MCL-1),与AML的发生和持续存在都有关联。MCL-1是未经治疗的AML患者样本中表达的主要BCL-2家族成员之一。MCL-1是癌症关键的细胞存活因子,通过直接影响细胞死亡途径导致化疗耐药。在此,我们综述MCL-1在AML中的作用,以及强效细胞周期蛋白依赖性激酶9抑制剂阿沃西地通过调控MCL-1可能成为针对该疾病合理治疗方法的机制。