Bishton Mark, Kenealy Melita, Johnstone Ricky, Rasheed Walid, Prince H Miles
Peter MacCallum Cancer Center, Department of Haematology, Melbourne, Australia.
Expert Rev Anticancer Ther. 2007 Oct;7(10):1439-49. doi: 10.1586/14737140.7.10.1439.
Chromatin modeling in DNA is fundamental to gene expression, DNA repair and replication. Methylation of promoter regions of tumor-suppressor genes and histone deacetylation leads to gene silencing and transcriptionally repressive chromatin. Histone deacetylase inhibitors and hypomethylating agents allow upregulation of proapoptotic genes and downregulation of antiapoptotic genes, and show significant single-agent anticancer activity, predominantly in cutaneous T-cell lymphoma and myelodysplasia, respectively. Combinations of these drugs are being employed in clinical trials to target multiple biological pathways, with the hope of synergistic pharmacodynamics. Preclinical studies of combinations of these agents with chemotherapy, monoclonal antibodies and small-molecule inhibitors are ongoing and demonstrate synergy in multiple hematological cancers, raising the prospect of future treatment for these diseases having a multitargeted approach.
DNA中的染色质建模对于基因表达、DNA修复和复制至关重要。肿瘤抑制基因启动子区域的甲基化和组蛋白去乙酰化会导致基因沉默和转录抑制性染色质。组蛋白去乙酰化酶抑制剂和低甲基化剂可上调促凋亡基因并下调抗凋亡基因,并分别在皮肤T细胞淋巴瘤和骨髓增生异常综合征中显示出显著的单药抗癌活性。这些药物的组合正在临床试验中用于靶向多种生物学途径,以期产生协同药效学作用。这些药物与化疗、单克隆抗体和小分子抑制剂联合使用的临床前研究正在进行中,并在多种血液系统癌症中显示出协同作用,为这些疾病未来采用多靶点治疗方法带来了希望。