Damsky W E, Bosenberg M
Department of Dermatology, Yale School of Medicine, New Haven, CT, USA.
Department of Pathology, Yale School of Medicine, New Haven, CT, USA.
Oncogene. 2017 Oct 19;36(42):5771-5792. doi: 10.1038/onc.2017.189. Epub 2017 Jun 12.
Approximately 33% of melanomas are derived directly from benign, melanocytic nevi. Despite this, the vast majority of melanocytic nevi, which typically form as a result of BRAF-activating mutations, will never progress to melanoma. Herein, we synthesize basic scientific insights and data from mouse models with common observations from clinical practice to comprehensively review melanocytic nevus biology. In particular, we focus on the mechanisms by which growth arrest is established after BRAF mutation. Means by which growth arrest can be overcome and how melanocytic nevi relate to melanoma are also considered. Finally, we present a new conceptual paradigm for understanding the growth arrest of melanocytic nevi in vivo termed stable clonal expansion. This review builds upon the canonical hypothesis of oncogene-induced senescence in growth arrest and tumor suppression in melanocytic nevi and melanoma.
大约33%的黑色素瘤直接源自良性黑素细胞痣。尽管如此,绝大多数通常由BRAF激活突变形成的黑素细胞痣永远不会发展成黑色素瘤。在此,我们综合了来自小鼠模型的基础科学见解和数据以及临床实践中的常见观察结果,以全面回顾黑素细胞痣生物学。特别是,我们关注BRAF突变后建立生长停滞的机制。还考虑了克服生长停滞的方法以及黑素细胞痣与黑色素瘤的关系。最后,我们提出了一种新的概念范式,用于理解体内黑素细胞痣的生长停滞,称为稳定克隆性扩增。本综述基于黑素细胞痣和黑色素瘤生长停滞及肿瘤抑制中癌基因诱导衰老的经典假说。