4.8 Review

Melanocytic nevi and melanoma: unraveling a complex relationship

Journal

ONCOGENE
Volume 36, Issue 42, Pages 5771-5792

Publisher

SPRINGERNATURE
DOI: 10.1038/onc.2017.189

Keywords

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Funding

  1. Melanoma Research Alliance
  2. Melanoma Research Foundation
  3. Hervey Family Foundation
  4. [R01 CA196660]
  5. [P50 CA121974]
  6. [P01CA128814]

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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 BRAFV600E-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 BRAFV600E 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.

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