WR-2721 protects against cytoxan-induced hprt mutagenesis without affecting therapeutic effectiveness
- Univ. of Chicago, Chicago, IL (United States). Dept. of Radiation and Cellular Oncology
- Argonne National Lab., IL (United States)
- Univ. of Texas, Houston, TX (United States)
- Univ. of Chicago, Chicadgo, IL (United States). Dept. of Radiation and Cellular Oncology
The radioprotector S-2-(3-aminopropylamino)ethylphosphorothioic acid (WR-2721) was evaluated for its ability to protect against cytoxan-induced mutagenesis at the hypoxanthine-guanine phosphoribosyl transferase (hprt) locus in mouse splenocytes under conditions that would not interfere with the therapeutic effectiveness of cytoxan in the treatment of fibrosarcoma lung tumors. Mutations at the hprt locus increase in frequency as a function of the dose of cytoxan used. With a spontaneous mutation frequency in C3H mice of 1.5 {times} 10{sup {minus}6}, mutation frequencies increased from 6.2 {times} 10{sup {minus}6} to 2.0 {times} 10{sup {minus}5} as the dose of cytoxan increased from 50 to 200 mg/kg. C3H male mice were injected in their tail veins with 3.5 {times} 10{sup 5} viable fibrosarcoma (FSa) cells. This protocol gave rise to an average of 68 tumor colonies per mouse. Four days following injection animals were treated with cytoxan at a dose of 100 mg/kg, which gave rise to significant tumor cell killing and a reduction in tumor colony number to less than an average of one per animal. WR-2721 at a concentration of 100 mg/kg did not affect on cytoxan`s therapeutic effectiveness. However, a 100 mg/kg dose of WR-2721 was effective in reducing the cytoxan induced hprt mutation frequency in mice from 160 to 35 per 10{sup 5} viable cells regardless of whether it was administered 30 min before or 2 h following cytoxan treatment.
- Research Organization:
- Argonne National Lab. (ANL), Argonne, IL (United States)
- Sponsoring Organization:
- USDOE, Washington, DC (United States); National Insts. of Health, Bethesda, MD (United States)
- DOE Contract Number:
- W-31109-ENG-38
- OSTI ID:
- 197829
- Report Number(s):
- ANL/CMB/CP-87504; CONF-9508206-1; ON: DE96005086; CNN: NIH/NCI CA-37435
- Resource Relation:
- Conference: 9. international conference on chemical modifiers of cancer treatment, Oxford (United Kingdom), 22-26 Aug 1995; Other Information: PBD: [1995]
- Country of Publication:
- United States
- Language:
- English
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