Intravesical liposomal muramyl tripeptide phosphatidylethanolamine treatment of human bladder carcinoma growing in nude mice

J Interferon Cytokine Res. 1995 Jun;15(6):585-92.

Abstract

The present study evaluated the in vivo activity of synthetic lipophilic muramyl tripeptide phosphatidylethanolamine (MTP-PE) when encapsulated into liposomes (phosphatidylcholine-phosphatidylserine, 7:3 molar ratio) and administered intravesically to athymic nude mice with human transitional cell carcinoma 253J-V cells growing in their bladder. Intravesical liposome-MTP-PE was effective in eradicating the human tumors implanted orthotopically in nude mice. Following therapy, activated macrophages were found in the bladders of liposome-MTP-PE-treated mice but not in control mice. In vitro activation of murine macrophages with liposome-MTP-PE increased their cytotoxicity against the 253J-V cell line used in these experiments. This effect was enhanced by cotreatment with interferon-gamma (IFN-gamma). Furthermore, cotreatment of macrophages with both liposome-MTP-PE and IFN-gamma resulted in the secretion of both tumor necrosis factor alpha (TNF-alpha) and interleukin-6 (IL-6). Liposome-encapsulated MTP-PE shows promise as an effective therapeutic agent for bladder carcinoma.

Publication types

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

MeSH terms

  • Acetylmuramyl-Alanyl-Isoglutamine / administration & dosage
  • Acetylmuramyl-Alanyl-Isoglutamine / analogs & derivatives*
  • Administration, Intravesical
  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Carcinoma, Transitional Cell / drug therapy*
  • Cell Division / drug effects
  • Cell Transplantation
  • Drug Carriers
  • Female
  • Humans
  • Liposomes
  • Macrophage Activation
  • Macrophages, Peritoneal / drug effects
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Phosphatidylethanolamines / administration & dosage*
  • Tumor Cells, Cultured
  • Urinary Bladder Neoplasms / drug therapy*

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • Liposomes
  • Phosphatidylethanolamines
  • mifamurtide
  • Acetylmuramyl-Alanyl-Isoglutamine