Energy metabolism in skin cancers: A therapeutic perspective

Biochim Biophys Acta Bioenerg. 2017 Aug;1858(8):712-722. doi: 10.1016/j.bbabio.2017.01.013. Epub 2017 Feb 1.

Abstract

Skin cancers are the most common cancers worldwide. The incidence of common skin cancers, including basal cell carcinomas (BCCs), squamous cell carcinomas (SCCs) and melanomas, continues to rise by 5 to 7% per year, mainly due to ultraviolet (UV) exposure and partly because of aging. This suggests an urgent necessity to improve the level of prevention and protection for skin cancers as well as developing new prognostic and diagnostic markers of skin cancers. Moreover, despite innovative therapies especially in the fields of melanoma and carcinomas, new therapeutic options are needed to bypass resistance to targeted therapies or treatment's side effects. Since reprogramming of cellular metabolism is now considered as a hallmark of cancer, some of the recent findings on the role of energy metabolism in skin cancer initiation and progression as well as its effect on the response to targeted therapies are discussed in this review. This article is part of a Special Issue entitled Mitochondria in cancer, edited by Giuseppe Gasparre, Rodrigue Rossignol and Pierre Sonveaux.

Keywords: BCC; Cancer biomarker; Carcinoma; Melanoma; Mitochondria; SCC; Targeted therapy; Warburg effect.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Carcinoma, Basal Cell / drug therapy
  • Carcinoma, Basal Cell / metabolism
  • Carcinoma, Basal Cell / prevention & control
  • Carcinoma, Squamous Cell / drug therapy
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / prevention & control
  • Cell Division / drug effects
  • DNA, Mitochondrial / genetics
  • Drug Resistance, Neoplasm
  • Energy Metabolism* / drug effects
  • Humans
  • Melanoma / drug therapy
  • Melanoma / metabolism
  • Melanoma / prevention & control
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / physiology
  • Neoplasm Proteins / antagonists & inhibitors
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Neoplasm Proteins / physiology
  • Oxidative Phosphorylation
  • Signal Transduction / drug effects
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / prevention & control

Substances

  • Antineoplastic Agents
  • DNA, Mitochondrial
  • Mitochondrial Proteins
  • Neoplasm Proteins