Brown Geoffrey, Hughes Philip
School of Immunity and Infection, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Leuk Res Treatment. 2012;2012:939021. doi: 10.1155/2012/939021. Epub 2012 Jun 12.
Many cancers arise in a tissue stem cell, and cell differentiation is impaired resulting in an accumulation of immature cells. The introduction of all-trans retinoic acid (ATRA) in 1987 to treat acute promyelocytic leukemia (APL), a rare subtype of acute myeloid leukemia (AML), pioneered a new approach to obtain remission in malignancies by restoring the terminal maturation of leukemia cells resulting in these cells having a limited lifespan. Differentiation therapy also offers the prospect of a less aggressive treatment by virtue of attenuated growth of leukemia cells coupled to limited damage to normal cells. The success of ATRA in differentiation therapy of APL is well known. However, ATRA does not work in non-APL AML. Here we examine some of the molecular pathways towards new retinoid-based differentiation therapy of non-APL AML. Prospects include modulation of the epigenetic status of ATRA-insensitive AML cells, agents that influence intracellular signalling events that are provoked by ATRA, and the use of novel synthetic retinoids.
许多癌症起源于组织干细胞,细胞分化受损,导致未成熟细胞积累。1987年,全反式维甲酸(ATRA)被引入用于治疗急性早幼粒细胞白血病(APL),这是急性髓系白血病(AML)的一种罕见亚型,开创了一种通过恢复白血病细胞的终末成熟来实现恶性肿瘤缓解的新方法,从而使这些细胞的寿命有限。分化疗法还提供了一种侵袭性较小的治疗前景,因为白血病细胞的生长减弱,对正常细胞的损害有限。ATRA在APL分化治疗中的成功是众所周知的。然而,ATRA在非APL AML中不起作用。在这里,我们研究了一些针对非APL AML基于新型维甲酸的分化疗法的分子途径。前景包括调节对ATRA不敏感的AML细胞的表观遗传状态、影响由ATRA引发的细胞内信号事件的药物,以及使用新型合成维甲酸。