Tigu Adrian Bogdan, Ivancuta Andrei, Uhl Andrada, Sabo Alexandru Cristian, Nistor Madalina, Mureșan Ximena-Maria, Cenariu Diana, Timis Tanase, Diculescu Doru, Gulei Diana
Department of Personalized Medicine and Rare Diseases, MEDFUTURE-Institute for Biomedical Research, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.
2nd Department of Obstetrics and Gynecology, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.
Biomedicines. 2025 May 13;13(5):1188. doi: 10.3390/biomedicines13051188.
Skin cancer prevalence has increased during the last decades, with the last years serving as a pivotal moment for comprehending its epidemiological patterns and its impact on public health. Melanoma is one of the most frequently occurring malignancies, arising from a complex interplay of genetic factors, environmental factors, lifestyle and socio-economic conditions. Epigenetic changes play a critical role in tumor development, influencing progression and aggressiveness. Epigenetic therapies could represent novel therapeutic options, while drug repositioning may serve as a viable strategy for cancer treatment. Demethylating agents, commonly used in hematological malignancies, show promising results on solid tumors, including melanoma. Methylation patterns are responsible for tumor development by modulating gene expression, while histone acetylation influences DNA processes such as transcription, replication, repair, and recombination. This review aims to identify existing potential therapeutical approaches using therapeutic agents that can modulate DNA methylation and histone modification, which can lead to tumor inhibition, cell death initiation and reactivation of tumor suppressor genes.
在过去几十年中,皮肤癌的患病率有所上升,最近几年成为理解其流行病学模式及其对公众健康影响的关键时刻。黑色素瘤是最常见的恶性肿瘤之一,由遗传因素、环境因素、生活方式和社会经济状况的复杂相互作用引起。表观遗传变化在肿瘤发展中起关键作用,影响肿瘤进展和侵袭性。表观遗传疗法可能代表新的治疗选择,而药物重新定位可能是癌症治疗的可行策略。常用于血液系统恶性肿瘤的去甲基化剂在包括黑色素瘤在内的实体瘤上显示出有前景的结果。甲基化模式通过调节基因表达负责肿瘤发展,而组蛋白乙酰化影响DNA过程,如转录、复制、修复和重组。本综述旨在确定使用可调节DNA甲基化和组蛋白修饰的治疗剂的现有潜在治疗方法,这可导致肿瘤抑制、细胞死亡启动和肿瘤抑制基因的重新激活。