• Media type: E-Article
  • Title: Low pH Does Not Affect the Dose Response for 5′-Amino-5′-Deoxythymidine Modulation of IdUrd DNA Incorporation and Radiosensitization in a Human Bladder Cancer Cell Line
  • Contributor: Kunugi, K. A.; Miller, E. M.; Vazquez-Padua, M. A.; Kinsella, T. J.
  • imprint: Academic Press, Inc., 1992
  • Published in: Radiation Research
  • Language: English
  • ISSN: 0033-7587; 1938-5404
  • Keywords: Symposium: The Molecular Basis for Radiation Effects on Cell Progression through the Cell Cycle
  • Origination:
  • Footnote:
  • Description: <p>We report that coincubation of 647V cells for one cell cycle with low concentrations (30 μM) of 5′-amino-5′-deoxythymidine increased IdUrd DNA incorporation and radiosensitivity at low extracellular pH &lt;tex-math&gt;$({\rm pH}_{{\rm e}}\ 6.8)$&lt;/tex-math&gt; in a fashion similar to treatment at normal pH&lt;sub&gt; e&lt;/sub&gt;. IdUrd DNA incorporation is inhibited by high (300 μM) 5′-AdThd concentrations at both normal and low pH&lt;sub&gt; e&lt;/sub&gt; (7.4 and 6.8), resulting in no significant radiosensitization. These results at low pH&lt;sub&gt; e&lt;/sub&gt; were not anticipated based on previously published studies of 5′-AdThd modulation of thymidine kinase (TK) activity and nucleoside cellular uptake. Our results suggest that regulation of intracellular pH ( pH&lt;sub&gt; i&lt;/sub&gt;) during the course of one cell cycle negates the 5′-AdThd dose-dependent modulation of TK activity demonstrated previously. Flow cytometric measurement of pH&lt;sub&gt; i&lt;/sub&gt; in 647V cells showed that normal pH&lt;sub&gt; i&lt;/sub&gt; (pH 7.4) was maintained in 647V cells over a 12- to 24-h exposure to low pH&lt;sub&gt; e&lt;/sub&gt; (pH 6.8). Thus the concomitant use of IdUrd and high concentrations of 5′-AdThd (&gt;30 μM) is unlikely to result in selective in vivo radiosensitization of human tumors under conditions which are intermittently or chronically acidic. However, low concentrations of 5′-AdThd may prove to be an effective in vivo modulator of IdUrd radiosensitization of human tumors under both normal and acidic conditions.</p>