Ghajar-Rahimi Gelare, Yusuf Nabiha
Department of Dermatology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Melanoma Manag. 2025 May 13;12(1):2505400. doi: 10.1080/20450885.2025.2505400. Epub 2025 May 16.
Cutaneous melanoma is a highly aggressive skin cancer with rising incidence, driven by risk factors such as ultraviolet exposure, genetic predisposition, and immunosuppression. While surgical excision remains the primary treatment, interest in chemoprevention strategies is growing. Numerous natural and synthetic agents have shown preclinical promise, but evaluating their effectiveness is challenging due to their systemic effects on multiple cell types. This review provides a focused examination of the melanocyte-specific mechanisms of select agents that have been tested in clinical trials for melanoma chemoprevention. We discuss various molecular and cellular mechanisms driving the anti-melanoma properties of nonsteroidal anti-inflammatory drugs, statins, sulforaphane, vitamin D, and -acetylcysteine. Despite promising preclinical and early clinical data, challenges remain regarding precise mechanisms, optimal dosing, long-term safety, and patient selection. Future research should focus on refining melanoma prevention strategies through well-designed clinical trials and personalized approaches integrating genetic and molecular risk factors.
皮肤黑色素瘤是一种侵袭性很强的皮肤癌,发病率呈上升趋势,其发病受紫外线暴露、遗传易感性和免疫抑制等风险因素驱动。虽然手术切除仍是主要治疗方法,但对化学预防策略的兴趣正在增加。许多天然和合成药物已显示出临床前的前景,但由于它们对多种细胞类型的全身作用,评估其有效性具有挑战性。本综述重点考察了在黑色素瘤化学预防临床试验中已测试的某些药物的黑素细胞特异性作用机制。我们讨论了驱动非甾体抗炎药、他汀类药物、萝卜硫素、维生素D和N - 乙酰半胱氨酸抗黑色素瘤特性的各种分子和细胞机制。尽管有前景良好的临床前和早期临床数据,但在精确机制、最佳剂量、长期安全性和患者选择方面仍存在挑战。未来的研究应通过精心设计的临床试验和整合遗传和分子风险因素的个性化方法,专注于完善黑色素瘤预防策略。