Combination of metallomics and proteomics to study the effects of the metallodrug RAPTA-T on human cancer cells.

Abstract

An approach to characterize the interactions of RAPTA-T, a novel ruthenium-based anticancer drug candidate with intriguing antimetastatic properties, with human ovarian cancer cells in vitro is described. The distribution profile of the metallodrug within the cancer cells was determined by (size exclusion chromatography)-inductively coupled mass spectrometry combined with subcellular fractionation procedures (metallomics). Multidimensional protein identification technology (MudPIT) was then used to obtain insight into the alteration of the cellular proteome upon RAPTA-T treatment. The metallomics approach reveals striking differences in the intracellular behavior of the drug between cisplatin-sensitive and resistant cell lines and provides clues on possible mechanisms of action as well as detoxification, quantitative proteomics based on spectral counting sheds light on cellular response mechanisms to metallodrug treatment.

• Authors: Dirk A Wolters, Maria Stefanopoulou, Paul J Dyson, Michael Groessl
• Journal: Metallomics : integrated biometal science (Metallomics) Vol. 4 Issue 11 Pg. 1185-96 (Nov 2012) ISSN: 1756-591X [Electronic] England
• PMID: 23014849 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Organometallic Compounds
• Proteome
• RAPTA-T
• Ruthenium
• DNA

Topics

• Antineoplastic Agents (chemistry, pharmacokinetics, pharmacology)
• Cell Line, Tumor
• DNA (metabolism)
• Female
• Humans
• Intracellular Space (drug effects, metabolism)
• Mass Spectrometry
• Mitochondria (drug effects, metabolism)
• Organometallic Compounds (chemistry, pharmacokinetics, pharmacology)
• Ovarian Neoplasms
• Proteome (analysis, drug effects)
• Proteomics
• Ruthenium (chemistry, pharmacokinetics, pharmacology)
• Tissue Distribution