Topical rapamycin inhibits tuberous sclerosis tumor growth in a nude mouse model

BMC Dermatol. 2008 Jan 28:8:1. doi: 10.1186/1471-5945-8-1.

Abstract

Background: Skin manifestations of Tuberous Sclerosis Complex (TSC) cause significant morbidity. The molecular mechanism underlying TSC is understood and there is evidence that systemic treatment with rapamycin or other mTOR inhibitors may be a useful approach to targeted therapy for the kidney and brain manifestations. Here we investigate topical rapamycin in a mouse model for TSC-related tumors.

Methods: 0.4% and 0.8% rapamycin ointments were applied to nude mice bearing subcutaneous, TSC-related tumors. Topical treatments were compared with injected rapamycin and topical vehicle. Rapamycin levels in blood and tumors were measured to assess systemic drug levels in all cohorts.

Results: Treatment with topical rapamycin improved survival and reduced tumor growth. Topical rapamycin treatment resulted in systemic drug levels within the known therapeutic range and was not as effective as injected rapamycin.

Conclusion: Topical rapamycin inhibits TSC-related tumor growth. These findings could lead to a novel treatment approach for facial angiofibromas and other TSC skin lesions.

Publication types

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

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Antibiotics, Antineoplastic / administration & dosage*
  • Antibiotics, Antineoplastic / pharmacokinetics
  • Cell Line, Tumor
  • Disease Models, Animal
  • Enzyme Inhibitors / administration & dosage*
  • Enzyme Inhibitors / pharmacokinetics
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Protein Kinases / drug effects*
  • Sirolimus / administration & dosage*
  • Sirolimus / pharmacokinetics
  • Skin Absorption
  • Soft Tissue Neoplasms / drug therapy*
  • Soft Tissue Neoplasms / metabolism
  • Soft Tissue Neoplasms / pathology
  • Survival Analysis
  • TOR Serine-Threonine Kinases
  • Tuberous Sclerosis / drug therapy*
  • Tuberous Sclerosis / metabolism
  • Tuberous Sclerosis / pathology

Substances

  • Antibiotics, Antineoplastic
  • Enzyme Inhibitors
  • Protein Kinases
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Sirolimus