Department of Pharmaceutical Biochemistry, Poznan University of Medical Sciences, 60-781 Poznań, Poland.
Genes (Basel). 2021 Jan 31;12(2):208. doi: 10.3390/genes12020208.
Cancer development involves both genetic and epigenetic alterations. Aberrant epigenetic modifications are reversible, allowing excellent opportunities for therapeutic intervention. Nowadays, several epigenetic drugs are used worldwide to treat, e.g., myelodysplastic syndromes and leukemias. However, overcoming resistance and widening the therapeutic profiles are the most important challenges faced by traditional epigenetic drugs. Recently, novel approaches to epigenetic therapies have been proposed. Next-generation epigenetic drugs, with longer half-life and better bioavailability, are being developed and tested. Since epigenetic phenomena are interdependent, treatment modalities include co-administration of two different epigenetic drugs. In order to sensitize cancer cells to chemotherapy, epigenetic drugs are administered prior to chemotherapy, or both epigenetic drug and chemotherapy are used together to achieve synergistic effects and maximize treatment efficacy. The combinations of epigenetic drug with immunotherapy are being tested, because they have proved to enhance antitumor immune responses. The next approach involves targeting the metabolic causes of epigenetic changes, i.e., enzymes which, when mutated, produce oncometabolites. Finally, epigenome editing makes it possible to modify individual chromatin marks at a defined region with unprecedented specificity and efficiency. This review summarizes the above attempts in fulfilling the promise of epigenetic drugs in the effective cancer treatment.
癌症的发生涉及遗传和表观遗传的改变。异常的表观遗传修饰是可逆的,这为治疗干预提供了极好的机会。如今,全球有几种表观遗传药物被用于治疗骨髓增生异常综合征和白血病等疾病。然而,克服耐药性和拓宽治疗谱是传统表观遗传药物面临的最重要挑战。最近,提出了新的表观遗传治疗方法。具有更长半衰期和更好生物利用度的下一代表观遗传药物正在开发和测试中。由于表观遗传现象是相互依存的,治疗方式包括两种不同的表观遗传药物联合使用。为了使癌细胞对化疗敏感,可以在化疗前给予表观遗传药物,或者同时使用表观遗传药物和化疗以达到协同作用并最大限度地提高治疗效果。正在测试表观遗传药物与免疫疗法的联合应用,因为它们已被证明可以增强抗肿瘤免疫反应。下一步是针对表观遗传变化的代谢原因,即当突变时产生致癌代谢物的酶。最后,表观基因组编辑使得在定义的区域以空前的特异性和效率修饰单个染色质标记成为可能。这篇综述总结了上述尝试,以实现表观遗传药物在有效癌症治疗中的承诺。