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PMID: 12128134 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Pronounced radiosensitization of cultured human cancer cells by COX inhibitor under acidic microenvironment.

International journal of radiation oncology, biology, physics ·Vol. 53 ·No. 5 ·2002-08-01 ·Pages 1314-8

Shah T, Ryu S, Lee HJ, Brown S, Kim JH

Abstract

To demonstrate the influence of pH on the cytotoxicity and radiosensitization by COX (cyclooxygenase) -1 and -2 inhibitors using established human cancer cells in culture. Nonselective COX inhibitor, ibuprofen (IB), and selective COX-2 inhibitor, SC-236, were used to determine the cytotoxicity and radiosensitization at varying pH of culture media. Human colon carcinoma cell line (HT-29) was exposed to the drug alone and in combination with radiation at different pH of the cell culture media. The end point was clonogenic ability of the single-plated cells after the treatment. Cytotoxicity and radiosensitization of IB increased with higher drug concentration and longer exposure time. The most significant radiosensitization was seen with IB (1.5 mM) for 2-h treatment at pH 6.7 before irradiation. The dose-modifying factor as defined by the ratio of radiation doses required to achieve the same effect on cell survival was 1.8 at 10% survival level. In contrast, SC-236 (50 microM for 2-8 h) showed no pH-dependent cytotoxicity. There was modest increase in the cell killing at lower doses of radiation. An acidic pH was an important factor affecting the increased cytotoxicity and radiosensitization by ibuprofen. Radiation response was enhanced at shoulder portion of the cell survival curve by selective COX-2 inhibitor.

MeSH Terms
Cell Survival Cyclooxygenase 1 Cyclooxygenase 2 Cyclooxygenase 2 Inhibitors Cyclooxygenase Inhibitors/pharmacology Dose-Response Relationship, Drug Humans Hydrogen-Ion Concentration Ibuprofen/pharmacology Isoenzymes/antagonists & inhibitors Membrane Proteins Prostaglandin-Endoperoxide Synthases Pyrazoles/pharmacology Radiation-Sensitizing Agents/pharmacology Sulfonamides/pharmacology Time Factors Tumor Cells, Cultured
Chemicals
4-(5-(4-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide Cyclooxygenase 2 Inhibitors Cyclooxygenase Inhibitors Isoenzymes Membrane Proteins Pyrazoles Radiation-Sensitizing Agents Sulfonamides Cyclooxygenase 1 Cyclooxygenase 2 PTGS1 protein, human PTGS2 protein, human Prostaglandin-Endoperoxide Synthases Ibuprofen
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shah Tushar
Department of Radiation Oncology, Henry Ford Hospital, Detroit, MI 48202, USA.
Ryu Samuel
Lee Ho Jun
Brown Stephen
Kim Jae Ho
Article Info
Journal
International journal of radiation oncology, biology, physics
Abbr.
Int J Radiat Oncol Biol Phys
ISSN
0360-3016
Published
2002-08-01
Pages
1314-8
Language
English
Region
United States
NLM ID
7603616
Subset
IM
Grants
NCI NIH HHS · CA-64323 · United States
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