TY - JOUR
T1 - Effect of acidic pH on radiosensitization of FSallC cells in vitro by misonidazole, etanidazole, or cis-diamminedichloroplatinum (II)
AU - Herman, T. S.
AU - Teicher, B. A.
AU - Pfeffer, M. R.
AU - Khandekar, V.
AU - Chapnick, R. M.
AU - Kalick, G. S.
AU - Rabow, A.
PY - 1990
Y1 - 1990
N2 - Because acidic regions may coexist with hypoxic regions in solid tumors, we have studied the effect of acidic extracellular pH on the abilities of misonidazole, etanidazole, and cis-diamminedichloroplatinum(II) (CDDP) to radiosensitize hypoxic FSaIIC cells in vitro. For 1-h exposures to misonidazole prior to and during irradiation, the sensitizer enhancement ratios (SERs) were 2.10 ± 0.18 at 1 mM drug and 2.50 ± 0.16 at 5 mM drug at pH 7.40 but only 1.90 ± 0.14 and 2.30 ± 0.14, respectively, at pH 6.45. For etanidazole the SERs at pH 7.40 at 1 and 5 mM drug were 1.90 ± 0.13 and 2.40 ± 0.18, respectively, but only 1.25 ± 0.13 and 1.70 ± 0.17, respectively, at pH 6.45. The decrease in the SERs for both 2-nitroimidazole compounds was statistically significant (P < 0.01). When CDDP at concentrations of 1 and 5 μM was tested. SERs of 1.30 ± 0.15 and 1.60 ± 0.18, respectively, were observed at pH 7.40, and the increase was not significant at pH 6.45 (1.35 ± 0.15 and 1.80 ± 0.19, respectively). The cellular levels of misonidazole, etanidazole, and CDDP did not vary significantly at the environmental conditions tested. These results demonstrate that pH is a potentially important variable in the action of hypoxic cell radiosensitizing drugs and suggest that future evaluations of such agents should test the effects of pH.
AB - Because acidic regions may coexist with hypoxic regions in solid tumors, we have studied the effect of acidic extracellular pH on the abilities of misonidazole, etanidazole, and cis-diamminedichloroplatinum(II) (CDDP) to radiosensitize hypoxic FSaIIC cells in vitro. For 1-h exposures to misonidazole prior to and during irradiation, the sensitizer enhancement ratios (SERs) were 2.10 ± 0.18 at 1 mM drug and 2.50 ± 0.16 at 5 mM drug at pH 7.40 but only 1.90 ± 0.14 and 2.30 ± 0.14, respectively, at pH 6.45. For etanidazole the SERs at pH 7.40 at 1 and 5 mM drug were 1.90 ± 0.13 and 2.40 ± 0.18, respectively, but only 1.25 ± 0.13 and 1.70 ± 0.17, respectively, at pH 6.45. The decrease in the SERs for both 2-nitroimidazole compounds was statistically significant (P < 0.01). When CDDP at concentrations of 1 and 5 μM was tested. SERs of 1.30 ± 0.15 and 1.60 ± 0.18, respectively, were observed at pH 7.40, and the increase was not significant at pH 6.45 (1.35 ± 0.15 and 1.80 ± 0.19, respectively). The cellular levels of misonidazole, etanidazole, and CDDP did not vary significantly at the environmental conditions tested. These results demonstrate that pH is a potentially important variable in the action of hypoxic cell radiosensitizing drugs and suggest that future evaluations of such agents should test the effects of pH.
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U2 - 10.2307/3577690
DO - 10.2307/3577690
M3 - Article
C2 - 2146699
AN - SCOPUS:0025223485
SN - 0033-7587
VL - 124
SP - 28
EP - 33
JO - Radiation Research
JF - Radiation Research
IS - 1
ER -