Dangerous liaisons: Loss of keratinocyte control over melanocytes in melanomagenesis

Kathleen J. Green*, Jenny Pokorny, Brieanna Jarrell

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

Abstract

Melanomas arise from transformed melanocytes, positioned at the dermal-epidermal junction in the basal layer of the epidermis. Melanocytes are completely surrounded by keratinocyte neighbors, with which they communicate through direct contact and paracrine signaling to maintain normal growth control and homeostasis. UV radiation from sunlight reshapes this communication network to drive a protective tanning response. However, repeated rounds of sun exposure result in accumulation of mutations in melanocytes that have been considered as primary drivers of melanoma initiation and progression. It is now clear that mutations in melanocytes are not sufficient to drive tumor formation—the tumor environment plays a critical role. This review focuses on changes in melanocyte-keratinocyte communication that contribute to melanoma initiation and progression, with a particular focus on recent mechanistic insights that lay a foundation for developing new ways to intercept melanoma development.

Original languageEnglish (US)
Article number2400135
JournalBioEssays
Volume46
Issue number11
DOIs
StatePublished - Nov 2024

Funding

Work in the authors labs is supported by R01AR041836, R01AR043380, R01CA228196, a Leo Foundation grant and the JL Mayberry endowment to KJG, and NIH/NCI F31CA281256 to JLP. The authors would also like to acknowledge support from the Northwestern University Skin Biology and Disease Resource-Based Center P30AR075049. The authors have no conflicts of interest to declare. Work in the authors labs is supported by R01AR041836, R01AR043380, R01CA228196, a Leo Foundation grant and the JL Mayberry endowment to KJG, and NIH/NCI F31CA281256 to JLP. The authors would also like to acknowledge support from the Northwestern University Skin Biology and Disease Resource\u2010Based Center P30AR075049. The authors have no conflicts of interest to declare.

Keywords

  • cadherin
  • Melanoma
  • pigmentation
  • tumor microenvironment
  • ultraviolet radiation

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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