Inhibition of bacterial multidrug resistance by celecoxib, a cyclooxygenase-2 inhibitor
- PMID: 20937780
- PMCID: PMC3019655
- DOI: 10.1128/AAC.00735-10
Inhibition of bacterial multidrug resistance by celecoxib, a cyclooxygenase-2 inhibitor
Abstract
Multidrug resistance (MDR) is a major problem in the treatment of infectious diseases and cancer. Accumulating evidence suggests that the cyclooxygenase-2 (COX-2)-specific inhibitor celecoxib would not only inhibit COX-2 but also help in the reversal of drug resistance in cancers by inhibiting the MDR1 efflux pump. Here, we demonstrate that celecoxib increases the sensitivity of bacteria to the antibiotics ampicillin, kanamycin, chloramphenicol, and ciprofloxacin by accumulating the drugs inside the cell, thus reversing MDR in bacteria.
Figures


References
-
- Arunasree, K. M., K. R. Roy, K. Anilkumar, A. Aparna, G. V. Reddy, and P. Reddanna. 2008. Imatinib-resistant K562 cells are more sensitive to celecoxib, a selective COX-2 inhibitor: role of COX-2 and MDR-1. Leuk. Res. 32:855-864. - PubMed
-
- Gupta, A. K., D. S. Chauhan, K. Srivastava, R. Das, S. Batra, M. Mittal, P. Goswami, N. Singhal, V. D. Sharma, K. Venkatesan, S. E. Hasnain, and V. M. Katoch. 2006. Estimation of efflux mediated multi-drug resistance and its correlation with expression levels of two major efflux pumps in mycobacteria. J. Commun. Dis. 38:246-254. - PubMed
-
- Kalle, A. M., S. Sachchidanand, and R. Pallu. 2010. Bcr-Abl-independent mechanism of resistance to imatinib in K562 cells: induction of cyclooxygenase-2 (COX-2) by histone deacetylases (HDACs). Leuk. Res. 34:1132-1138. - PubMed
-
- Kern, W. V., P. Steinke, A. Schumacher, S. Schuster, H. von Baum, and J. A. Bohnert. 2006. Effect of 1-(1-naphthylmethyl)-piperazine, a novel putative efflux pump inhibitor, on antimicrobial drug susceptibility in clinical isolates of Escherichia coli. J. Antimicrob. Chemother. 57:339-343. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials