Improved radiosensitization of rat glioma cells with adenovirus-expressed mutant herpes simplex virus-thymidine kinase in combination with acyclovir

• DOI: 10.1038/sj.cgt.7700185
• Publication Date: 2002-09-04T16:13:01Z
• Authors: Kristoffer Valerie; David Brust; Julie Farnsworth; Cyrus Amir; Mohiuddin M Taher; Chad Hershey; Jeffrey Feden
• Keywords: Dose-Response Relationship, Drug; Brain Neoplasms; Blotting, Western; Genetic Vectors; Acyclovir; Apoptosis; Dose-Response Relationship, Radiation; Glioma; Antiviral Agents; Combined Modality Therapy; Thymidine Kinase; Rats, Inbred F344; Adenoviridae; Rats; 3. Good health; 03 medical and health sciences; 0302 clinical medicine; Mutation; Tumor Cells, Cultured; Animals; Simplexvirus

Adenovirus expressing herpes simplex virus-thymidine kinase (HSV-TK) sensitizes internal rat glioma cells to radiation in combination with acyclovir (ACV). However, relatively high concentrations of ACV (>10 microM) are required to obtain significant radiosensitization. Serum levels rarely reach more than the lower micromolar range, preventing the full use of this genetic approach to radiosensitize cells in vivo. To better use the lower concentrations of ACV available in sera, we constructed an adenovirus expressing a mutant HSV-TK (HSV-TK(75)) isolated for its approximately 20 times greater sensitivity to ACV than wild-type (wt) HSV-TK. We demonstrate that rat RT2 glioma cells infected with adenovirus AdCMV-TK(75) and exposed to either ACV or ganciclovir become more sensitive to lower concentrations (1-3 microM) of the drugs compared with cells infected with AdCMV-TK(wt), which expresses wt HSV-TK. Most importantly, the RT2 cells become more sensitive to low doses (2-4 Gy) of 60Co radiation than cells infected with an adenovirus expressing wt HSV-TK. This sensitization is accompanied by an increased rate of apoptosis. In summary, we show that infection of rat glioma cells with an adenovirus expressing a mutant HSV-TK sensitizes the cells to low doses of radiation after exposure to ACV at lower concentrations than those required for wt HSV-TK. This finding suggests that this mutant adenovirus may improve the in vivo efficacy of HSV-TK-based cancer gene therapy approaches.