Metabolomic profiling of the synergistic effects of melittin in combination with cisplatin on ovarian cancer cells
Alonezi, Sanad and Tusiimire, Jonans and Wallace, Jennifer and Dufton, Mark J. and Parkinson, John A. and Young, Louise C. and Clements, Carol J. and Park, Jin-Kyu and Jeon, Jong-Woon and Ferro, Valerie A. and Watson, David G. (2017) Metabolomic profiling of the synergistic effects of melittin in combination with cisplatin on ovarian cancer cells. Metabolites, 7 (14). pp. 1-18. ISSN 2218-1989 (https://doi.org/10.3390/metabo7020014)
Preview |
Text.
Filename: Alonezi_etal_Metabolites2017_Metabolomic_profiling_of_the_synergistic_effects_of_melittin.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
Melittin, the main peptide present in bee venom, has been proposed as having potential for anticancer therapy; the addition of melittin to cisplatin, a first line treatment for ovarian cancer, may increase the therapeutic response in cancer treatment via synergy, resulting in improved tolerability, reduced relapse, and decreased drug resistance. Thus, this study was designed to compare the metabolomic effects of melittin in combination with cisplatin in cisplatin-sensitive (A2780) and resistant (A2780CR) ovarian cancer cells. Liquid chromatography (LC) coupled with mass spectrometry (MS) was applied to identify metabolic changes in A2780 (combination treatment 5 μg/mL melittin + 2 μg mL cisplatin) and A2780CR (combination treatment 2 μg/mL melittin + 10 μg/mL cisplatin) cells. Principal components analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA) multivariate data analysis models were produced using SIMCA-P software. All models displayed good separation between experimental groups and high-quality goodness of fit (R2) and goodness of prediction (Q2), respectively. The combination treatment induced significant changes in both cell lines involving reduction in the levels of metabolites in the tricarboxylic acid (TCA) cycle, oxidative phosphorylation, purine and pyrimidine metabolism, and the arginine/proline pathway. The combination of melittin with cisplatin that targets these pathways had a synergistic effect. The melittin-cisplatin combination had a stronger effect on the A2780 cell line in comparison with the A2780CR cell line. The metabolic effects of melittin and cisplatin in combination were very different from those of each agent alone.
ORCID iDs
Alonezi, Sanad ORCID: https://orcid.org/0000-0003-3009-272X, Tusiimire, Jonans ORCID: https://orcid.org/0000-0002-5831-1499, Wallace, Jennifer ORCID: https://orcid.org/0000-0003-4165-3393, Dufton, Mark J. ORCID: https://orcid.org/0000-0001-8176-2194, Parkinson, John A. ORCID: https://orcid.org/0000-0003-4270-6135, Young, Louise C., Clements, Carol J., Park, Jin-Kyu, Jeon, Jong-Woon, Ferro, Valerie A. ORCID: https://orcid.org/0000-0003-1967-3603 and Watson, David G. ORCID: https://orcid.org/0000-0003-1094-7604;-
-
Item type: Article ID code: 60451 Dates: DateEvent14 April 2017Published12 April 2017AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Faculty of Science > Pure and Applied ChemistryDepositing user: Pure Administrator Date deposited: 18 Apr 2017 09:50 Last modified: 15 Dec 2024 01:23 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/60451