Advances in acute myeloid leukemia differentiation therapy: A critical review

被引:14
作者
Abdel-Aziz, Amal Kamal [1 ,2 ]
机构
[1] Ain Shams Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo 11566, Egypt
[2] King Abdullah Univ Sci & Technol KAUST, Biol & Environm Sci & Engn Div, Smart Hlth Initiat, Thuwal 23955, Saudi Arabia
关键词
AML; Dedifferentiation; LSC; Resistance; Relapse; Remission; TRANS-RETINOIC ACID; VALPROIC ACID; DNA METHYLATION; CELL-DIFFERENTIATION; INHIBITORS; AZACITIDINE; COMBINATION; MODELS; FLT3; RISK;
D O I
10.1016/j.bcp.2023.115709
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute myeloid leukemia (AML) is characterized by impaired differentiation and indefinite proliferation of abnormal myeloid progenitors. Although differentiating agents were deemed to revolutionize AML therapy, most treated non-APL AML patients are refractory or relapse. According to cancer stem cell model, leukemia-initiating cells are the root cause of relapse given their unidirectional potential to generate differentiated AML blasts. Nonetheless, accumulating evidences emphasize the de-differentiation plasticity and leukemogenic potential of mature AML blasts and the frailty of targeting leukemic stem cells per se. This review critically discusses the potential and challenges of (lessons learnt from) conventional and novel differentiating agents in AML therapy. Although differentiating agents might hold promise, they should be exploited within the context of a rationale combination regimen eradicating all maturation/differentiation states of AML cells. The results of the routinely used immunophenotypic markers and/or morphological analyses of differentiation should be carefully interpreted given their propensity to underestimate AML burden.
引用
收藏
页数:11
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