Hung Christie, Nguyen Trang T T, Poulikakos Poulikos I, Polsky David
Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, Laura and Isaac Perlmutter Cancer Center, NYU Langone Health, New York, NY 10016, USA.
Department of Oncological Sciences, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Cancers (Basel). 2025 Apr 11;17(8):1291. doi: 10.3390/cancers17081291.
Melanoma is an aggressive cancer with rising incidence, particularly among older individuals. Despite advancements in targeted therapies for BRAF and MEK proteins and immunotherapies, many patients either fail to respond or develop resistance. For those progressing on immunotherapy, limited treatment options remain. The Cyclin D-CDK4/6-RB pathway is commonly dysregulated in melanoma, with up to 90% of cases showing alterations that activate it. Although targeting Cyclin-CDK complexes has shown promise in preclinical models, clinical responses have been suboptimal. This review explores the molecular mechanisms behind Cyclin-CDK dysregulation in melanoma and the challenges of targeting this pathway. It also discusses strategies to improve the efficacy of CDK4/6 inhibitors, including combination therapies to overcome resistance and enhance patient outcomes. Understanding these mechanisms can guide the development of more effective treatments for melanoma.
黑色素瘤是一种侵袭性癌症,发病率不断上升,在老年人中尤为明显。尽管针对BRAF和MEK蛋白的靶向治疗以及免疫治疗取得了进展,但许多患者要么没有反应,要么产生耐药性。对于那些在免疫治疗中进展的患者,治疗选择仍然有限。细胞周期蛋白D - CDK4/6 - RB通路在黑色素瘤中通常失调,高达90%的病例显示出激活该通路的改变。尽管在临床前模型中靶向细胞周期蛋白 - CDK复合物已显示出前景,但临床反应并不理想。本综述探讨了黑色素瘤中细胞周期蛋白 - CDK失调背后的分子机制以及靶向该通路的挑战。它还讨论了提高CDK4/6抑制剂疗效的策略,包括联合治疗以克服耐药性并改善患者预后。了解这些机制可以指导开发更有效的黑色素瘤治疗方法。