Translating cyclooxygenase signaling in patch heterozygote mice into a randomized clinical trial in basal cell carcinoma

Cancer Prev Res (Phila). 2010 Jan;3(1):4-7. doi: 10.1158/1940-6207.CAPR-09-0246.

Abstract

This different perspective on Tang et al. (beginning on p. 25 in this issue of the journal) discusses the pivotal role of cyclooxygenase (COX) signaling in the pathogenesis of basal cell carcinoma (BCC). These investigators conducted elegant experiments showing increased BCC burden in patch heterozygous mice overexpressing COX-2 in the epidermis. Genetic deletion of COX-1 or COX-2 resulted in a robust decrease in BCC burden in patch heterozygote mice. They then studied pharmacologic COX inhibition in mice and humans with loss of patch, finding a trend in humans toward decreased BCC burden. This finding has implications for public health.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review
  • Comment

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma, Basal Cell / drug therapy*
  • Carcinoma, Basal Cell / enzymology
  • Carcinoma, Basal Cell / genetics
  • Heterozygote
  • Humans
  • Mice
  • Patched Receptors
  • Randomized Controlled Trials as Topic*
  • Receptors, Cell Surface / genetics*
  • Signal Transduction / physiology*
  • Skin Neoplasms / drug therapy*
  • Skin Neoplasms / enzymology
  • Skin Neoplasms / genetics

Substances

  • Antineoplastic Agents
  • Patched Receptors
  • Receptors, Cell Surface