Nowak Daniel, Stewart Daphne, Koeffler H Phillip
Division of Hematology and Oncology, Cedars Sinai Medical Center, University of California Los Angeles (UCLA) School of Medicine, CA 90048, USA.
Blood. 2009 Apr 16;113(16):3655-65. doi: 10.1182/blood-2009-01-198911. Epub 2009 Feb 12.
A characteristic feature of leukemia cells is a blockade of differentiation at a distinct stage in cellular maturation. In the 1970s and 1980s, studies demonstrating the capabilities of certain chemicals to induce differentiation of hematopoietic cell lines fostered the concept of treating leukemia by forcing malignant cells to undergo terminal differentiation instead of killing them through cytotoxicity. The first promising reports on this notion prompted a review article on this subject by us 25 years ago. In this review, we revisit this interesting field of study and report the progress achieved in the course of nearly 3 decades. The best proof of principle for differentiation therapy has been the treatment of acute promyelocytic leukemia with all-trans retinoic acid. Attempts to emulate this success with other nuclear hormone ligands such as vitamin D compounds and PPARgamma agonists or different classes of substances such as hematopoietic cytokines or compounds affecting the epigenetic landscape have not been successful on a broad scale. However, a multitude of studies demonstrating partial progress and improvements and, finally, the new powerful possibilities of forward and reverse engineering of differentiation pathways by manipulation of transcription factors support the continued enthusiasm for differentiation therapy of leukemia in the future.
白血病细胞的一个特征是在细胞成熟的特定阶段出现分化阻滞。在20世纪70年代和80年代,一些研究表明某些化学物质能够诱导造血细胞系分化,这催生了通过迫使恶性细胞进行终末分化而非通过细胞毒性杀死它们来治疗白血病的概念。25年前,关于这一概念的首批有前景的报告促使我们撰写了一篇关于该主题的综述文章。在这篇综述中,我们重新审视这个有趣的研究领域,并报告近30年来所取得的进展。分化疗法的最佳原理证明是用全反式维甲酸治疗急性早幼粒细胞白血病。试图用其他核激素配体(如维生素D化合物和PPARγ激动剂)或不同类别的物质(如造血细胞因子或影响表观遗传格局的化合物)来效仿这一成功,但在广泛范围内并未成功。然而,大量研究显示出部分进展和改进,最终,通过操纵转录因子对分化途径进行正向和反向工程的新强大可能性,支持了未来对白血病分化疗法持续的热情。