Bhalla Kapil N
Department of Interdisciplinary Oncology, H. Lee Moffitt Cancer Center and Research Institute University of South Florida, Tampa, FL 33612, USA.
J Clin Oncol. 2005 Jun 10;23(17):3971-93. doi: 10.1200/JCO.2005.16.600. Epub 2005 May 16.
Epigenetic regulation of gene expression is mediated through alterations in the DNA methylation status, covalent modifications of core nucleosomal histones, rearrangement of histones, and by RNA interference. It is now abundantly clear that deregulation of epigenetic mechanisms cooperates with genetic alterations in the development and progression of cancer and leukemia. Epigenetic deregulation affects several aspects of tumor cell biology, including cell growth, cell cycle control, differentiation, DNA repair, and cell death. This raises the strong possibility that reversing deregulated epigenetic mechanisms may be an effective treatment strategy for leukemia and cancer. This treatment strategy may either be designed to separately or collectively target the specific perturbations in the epigenetic mechanisms found in human hematologic malignancies. The following review describes our current understanding of the important deregulated epigenetic mechanisms and the preclinical and clinical development of epigenetic and chromatin modifiers in the therapy of these disorders.
基因表达的表观遗传调控是通过DNA甲基化状态的改变、核心核小体组蛋白的共价修饰、组蛋白的重排以及RNA干扰介导的。现在已经非常清楚,表观遗传机制的失调与癌症和白血病发生发展过程中的基因改变相互协作。表观遗传失调影响肿瘤细胞生物学的多个方面,包括细胞生长、细胞周期控制、分化、DNA修复和细胞死亡。这极大地增加了逆转失调的表观遗传机制可能成为白血病和癌症有效治疗策略的可能性。这种治疗策略可以设计为单独或共同针对人类血液系统恶性肿瘤中发现的表观遗传机制的特定扰动。以下综述描述了我们目前对重要的失调表观遗传机制的理解,以及表观遗传和染色质修饰剂在这些疾病治疗中的临床前和临床进展。