MKT-077, a novel rhodacyanine dye in clinical trials, exhibits anticarcinoma activity in preclinical studies based on selective mitochondrial accumulation

Cancer Res. 1996 Feb 1;56(3):538-43.

Abstract

MKT-077 (formerly known as FJ-776) is a newly synthesized, highly water-soluble ( > 200 mg/ml) rhodacyanine dye that exhibits significant antitumor activity in a variety of model systems. In culture, MKT-077 inhibits the growth of five human cancer cell lines (colon carcinoma CX-1, breast carcinoma MCF-7, pancreatic carcinoma (CRL 1420, bladder transitional cell carcinoma EJ, and melanoma LOX) but not monkey kidney CV-1, an indicator cell line for normal epithelial cells. In nude mice, MKT-077 inhibits the growth of s.c. implanted human renal carcinoma A498 and human prostate carcinoma DU145 and prolongs the survival of mice bearing i.p. implanted human melanoma LOX (tumor:control = 344%). Subcellular localization indicates that MKT-077 is taken up and retained by mitochondria, and flow cytometric analysis suggests that CX-1 cells take up MKT-077 to a much greater extent than CV-1 cells. Quantitation of MKT-077 uptake by ethanol extraction shows that CX-1 cells accumulate 65-fold more MKT-077 than do CV-1 cells. MKT-077 is the first delocalized lipophilic cation with a favorable pharmacological and toxicological profile in preclinical studies. MKT-077 is now being investigated in Phase I clinical trials.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacokinetics*
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / toxicity
  • Cell Division / drug effects
  • Cell Line
  • Chlorocebus aethiops
  • Cisplatin / pharmacokinetics
  • Cisplatin / pharmacology
  • Doxorubicin / pharmacokinetics
  • Doxorubicin / pharmacology
  • Drug Screening Assays, Antitumor
  • Ethanol / chemistry
  • Female
  • Flow Cytometry
  • Humans
  • Kidney / drug effects
  • Male
  • Mice
  • Mice, Nude
  • Microscopy, Confocal
  • Microscopy, Video
  • Mitochondria / metabolism*
  • Neoplasm Transplantation
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Pyridines / pharmacology*
  • Pyridines / toxicity
  • Solubility
  • Thiazoles / pharmacology*
  • Thiazoles / toxicity
  • Tumor Cells, Cultured / drug effects

Substances

  • Antineoplastic Agents
  • Pyridines
  • Thiazoles
  • Ethanol
  • Doxorubicin
  • MKT 077
  • Cisplatin