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Combination of atorvastatin and celecoxib synergistically induces cell cycle arrest and apoptosis in colon cancer cells
- Source :
- International Journal of Cancer. 122:2115-2124
- Publication Year :
- 2008
- Publisher :
- Wiley, 2008.
-
Abstract
- Previous studies in animal models have shown enhanced efficacy of a combined treatment of statins and Nonsteroidal anti-inflammatory drugs against colorectal cancer development. In our study, we investigated the combinational effects of atorvastatin and celecoxib in 2 human colon cancer cell lines HCT116 and HT29. Celecoxib moderately inhibited the growth of both cell lines with a similar IC(50) of 40-50 microM, whereas atorvastatin showed stronger growth inhibitory effect in HCT116 cells than in HT29 cells (IC(50) of 5-8 microM vs. 30-35 microM) after treatment for 48-72 hr. The combination of these 2 agents produced strong synergistic actions, as determined by isobologram analysis. Flow cytometry analysis indicated that the combination treatment for 24 hr caused extensive cell cycle arrest in G0/G1 phase; whereas at 48 hr or longer, apoptosis was induced significantly. The effects produced by the combination were much stronger than that by atorvastatin or celecoxib alone. Our results further demonstrated that the combinational effects of atorvastatin/celecoxib were associated with increased levels of p21(Cip1/Waf1), p27(Kip1), and phospho-JNK; decreased levels of phospho-AKT and hyper-phosphorylated Rb; and activation of caspase cascade. Atorvastatin/celecoxib combination also selectively modified membrane localization of small G-proteins, such as RhoA, RhoB and RhoC, which may contribute to the anti-cancer effects. Taken together, the results demonstrated a strong synergy between the actions of atorvastatin and celecoxib in growth inhibition and killing of human colon cancer cells. The present work suggests the possible therapeutic application of this combination and provides leads for mechanistic and biomarker investigations in clinical trials.
- Subjects :
- Cancer Research
medicine.medical_specialty
Programmed cell death
Time Factors
Cell cycle checkpoint
Cell Survival
MAP Kinase Kinase 4
Colorectal cancer
Atorvastatin
Immunoblotting
Apoptosis
Pharmacology
Resting Phase, Cell Cycle
chemistry.chemical_compound
GTP-Binding Proteins
Internal medicine
medicine
Humans
Cyclooxygenase Inhibitors
Pyrroles
neoplasms
Sulfonamides
Dose-Response Relationship, Drug
business.industry
Cell Cycle
G1 Phase
Drug Synergism
Cell cycle
HCT116 Cells
medicine.disease
Endocrinology
Oncology
chemistry
Celecoxib
Heptanoic Acids
Colonic Neoplasms
Pyrazoles
Drug Therapy, Combination
lipids (amino acids, peptides, and proteins)
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Growth inhibition
business
HT29 Cells
Proto-Oncogene Proteins c-akt
Signal Transduction
medicine.drug
Subjects
Details
- ISSN :
- 00207136
- Volume :
- 122
- Database :
- OpenAIRE
- Journal :
- International Journal of Cancer
- Accession number :
- edsair.doi.dedup.....d87073ab5167adf97abf2630a51915b2