髓系白血病
医学
白血病
癌症研究
髓样
淋巴瘤
肿瘤科
免疫学
内科学
作者
Tapan M. Kadia,Hagop M. Kantarjian,Marina Konopleva
出处
期刊:Oncotarget
[Impact Journals LLC]
日期:2019-02-08
卷期号:10 (12): 1250-1265
被引量:18
标识
DOI:10.18632/oncotarget.26579
摘要
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.
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