From basal cell carcinoma morphogenesis to the alopecia induced by hedgehog inhibitors: connecting the dots

Br J Dermatol. 2017 Dec;177(6):1485-1494. doi: 10.1111/bjd.15738. Epub 2017 Oct 25.

Abstract

The deciphering of the hedgehog (Hh) signalling pathway implicated in the tumorigenesis of basal cell carcinoma (BCC) led to the development of targeted drug therapies, the Hh pathway inhibitors (HPIs) vismodegib and sonidegib. In the skin, physiological Hh signalling is activated in growing hair follicles (HFs), where it is required for proliferation of the epithelium of HFs during morphogenesis and for their postnatal growth. The effects of HPI treatment leading to the regression of BCC and the development of alopecia underpin the central role of the Hh pathway in BCC formation, as well as hair cycling. Given the fact that BCC is a follicular-driven tumour, it is a fine tuning of events that regulate hair cycling that may drive towards the formation of benign follicular hamartomas or malignant BCC neoplasms. Wnt/β-catenin signalling interacts with the Hh signalling during HF morphogenesis, normal hair cycling and BCC development. The aim of this review is to present how key molecular events implicated in Hh pathway crosstalk in the HF are also involved in BCC pathogenesis and result in the alopecia developed by HPI treatment.

Publication types

  • Review

MeSH terms

  • Alopecia / chemically induced*
  • Carcinogenesis / pathology
  • Carcinoma, Basal Cell / pathology*
  • Hair Follicle / embryology
  • Hair Follicle / growth & development
  • Hedgehog Proteins / antagonists & inhibitors*
  • Hedgehog Proteins / pharmacology
  • Humans
  • Morphogenesis / physiology
  • Signal Transduction / physiology
  • Skin Neoplasms / pathology*
  • beta Catenin / metabolism

Substances

  • Hedgehog Proteins
  • beta Catenin