HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Molecular pharmacodynamics of PM02734 (elisidepsin) as single agent and in combination with erlotinib; synergistic activity in human non-small cell lung cancer cell lines and xenograft models.

Abstract
PM02734 (elisidepsin) is a novel marine-derived cyclic peptide belonging to the Kahalalide family of compounds currently under phase I development with early evidence of a positive therapeutic index. The cytotoxicity of PM02734 has been determined in a panel of human NSCLC (non-small cell lung cancer) cell lines. Western blot analysis showed a direct correlation between ErbB3 expression and cell sensitivity to PM02734. Furthermore, PM02734 was more effective in the induction of ErbB3 degradation and dephosphorylation than in that of ErbB2 and ErbB1 in human NSCLC cell lines. The combination of PM02734 and erlotinib was synergistic in all NSCLC cell lines tested, including erlotinib resistant cell lines, with combination indexes ranging between 0.59 and 0.81. The combination of PM02734 and erlotinib was more effective than either drug alone in mice inoculated intravenously (i.v.) with A549 cells. The combination of PM02734 and erlotinib was more effective in inhibiting AKT than either single agent alone in H322 cells. These results have provided a rational basis for an ongoing clinical trial to explore this combination in patients with advanced malignant solid tumours.
AuthorsYi-He Ling, Miguel Aracil, José Jimeno, Roman Perez-Soler, Yiyu Zou
JournalEuropean journal of cancer (Oxford, England : 1990) (Eur J Cancer) Vol. 45 Issue 10 Pg. 1855-64 (Jul 2009) ISSN: 1879-0852 [Electronic] England
PMID19346126 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Depsipeptides
  • Oncogene Proteins v-erbB
  • Protein Kinase Inhibitors
  • Quinazolines
  • elisidepsin
  • Erlotinib Hydrochloride
Topics
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Antineoplastic Combined Chemotherapy Protocols (pharmacology)
  • Carcinoma, Non-Small-Cell Lung (drug therapy, metabolism, pathology, secondary)
  • Cell Death (drug effects)
  • Cell Survival (drug effects)
  • Depsipeptides (administration & dosage, pharmacology)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Erlotinib Hydrochloride
  • Humans
  • Lung Neoplasms (drug therapy, metabolism, pathology)
  • Mice
  • Mice, Nude
  • Oncogene Proteins v-erbB (metabolism)
  • Protein Kinase Inhibitors (administration & dosage, pharmacology)
  • Quinazolines (administration & dosage, pharmacology)
  • Signal Transduction (drug effects)
  • Tumor Cells, Cultured
  • Xenograft Model Antitumor Assays (methods)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: