Montalvo-Casimiro Michel, González-Barrios Rodrigo, Meraz-Rodriguez Marco Antonio, Juárez-González Vasti Thamara, Arriaga-Canon Cristian, Herrera Luis A
Unidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología-Instituto de Investigaciones Biomédicas, UNAM, Mexico City, Mexico.
Departamento de Bioquímica, Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Front Oncol. 2020 Nov 18;10:605386. doi: 10.3389/fonc.2020.605386. eCollection 2020.
Gene mutations are strongly associated with tumor progression and are well known in cancer development. However, recently discovered epigenetic alterations have shown the potential to greatly influence tumoral response to therapy regimens. Such epigenetic alterations have proven to be dynamic, and thus could be restored. Due to their reversible nature, the promising opportunity to improve chemotherapy response using epigenetic therapy has arisen. Beyond helping to understand the biology of the disease, the use of modern clinical epigenetics is being incorporated into the management of the cancer patient. Potential epidrug candidates can be found through a process known as drug repositioning or repurposing, a promising strategy for the discovery of novel potential targets in already approved drugs. At present, novel epidrug candidates have been identified in preclinical studies and some others are currently being tested in clinical trials, ready to be repositioned. This epidrug repurposing could circumvent the classic paradigm where the main focus is the development of agents with one indication only, while giving patients lower cost therapies and a novel precision medical approach to optimize treatment efficacy and reduce toxicity. This review focuses on the main approved epidrugs, and their druggable targets, that are currently being used in cancer therapy. Also, we highlight the importance of epidrug repurposing by the rediscovery of known chemical entities that may enhance epigenetic therapy in cancer, contributing to the development of precision medicine in oncology.
基因突变与肿瘤进展密切相关,在癌症发展过程中广为人知。然而,最近发现的表观遗传改变已显示出极大影响肿瘤对治疗方案反应的潜力。此类表观遗传改变已被证明具有动态性,因此可以恢复。由于其可逆性,利用表观遗传疗法改善化疗反应的前景应运而生。除了有助于理解疾病生物学外,现代临床表观遗传学的应用正被纳入癌症患者的管理中。潜在的表观遗传药物候选物可通过一种称为药物重新定位或重新用途开发的过程找到,这是在已批准药物中发现新潜在靶点的一种有前景的策略。目前,在临床前研究中已鉴定出新型表观遗传药物候选物,其他一些正在临床试验中进行测试,准备重新定位。这种表观遗传药物重新用途开发可以规避主要关注仅有一种适应症药物开发的经典模式,同时为患者提供成本更低的治疗方法以及一种新型精准医疗方法,以优化治疗效果并降低毒性。本综述重点关注目前用于癌症治疗的主要已批准表观遗传药物及其可成药靶点。此外,我们强调通过重新发现可能增强癌症表观遗传治疗的已知化学实体来进行表观遗传药物重新用途开发的重要性,这有助于肿瘤学精准医学的发展。