Hypoxic cell cytotoxin tirapazamine induces acute changes in tumor energy metabolism and pH:A31p magnetic resonance spectroscopy study
Autor: | Zaver M. Bhujwalla, Ding Jen Lee, Larry E. Dillehay, Eric O. Aboagye |
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Rok vydání: | 1998 |
Předmět: |
chemistry.chemical_classification
Radiation Radiological and Ultrasound Technology Bioenergetics Intracellular pH Nuclear magnetic resonance spectroscopy Molecular biology chemistry.chemical_compound Oncology Mechanism of action chemistry Biochemistry In vivo Pi medicine Radiology Nuclear Medicine and imaging Nucleotide medicine.symptom Tirapazamine |
Zdroj: | Radiation Oncology Investigations. 6:249-254 |
ISSN: | 1520-6823 1065-7541 |
DOI: | 10.1002/(sici)1520-6823(1998)6:6<249::aid-roi1>3.0.co;2-c |
Popis: | Tirapazamine is a hypoxic cell cytotoxin in phase II/III trials. To further understand its mechanism of action in vivo, we examined the effect of tirapazamine on tumor energy metabolism and pH. RIF-1 and SCCVII tumors were grown subcutaneously in the flanks of C3H mice. Tumor energy metabolism, expressed as the ratio of inorganic phosphate to nucleotide triphosphate (Pi/NTP), and intracellular pH (pHi), were measured by 31P magnetic resonance spectroscopy (MRS). In RIF-1 and SCCVII tumors, tirapazamine increased the Pi/NTP ratio by 2.6-fold and 3-fold, respectively, within the first hour after an intraperitoneal dose of 0.3 mmol/kg. A corresponding decrease in pHi from 7.05+/-0.07 to 6.48+/-0.06, and 7.21+/-0.09 to 6.45+/-0.02 in RIF-1 and SCCVII tumors, respectively, was observed. The decrease in tumor 31P bioenergetics and pH was reversible, as exemplified by RIF-1 tumors, which showed a further increase in Pi/NTP ratio of 3.5-fold by 5-8 hr, returning to normal range at 24 hr. Corresponding pHi of RIF-1 tumors was 6.88+/-0.05 at 5-8 hr and 7.16+/-0.05 at 24 hr. We concluded that tirapazamine induces acute changes in tumor energy metabolism and pHi. These findings are relevant to the rational selection and optimal timing of coadministered therapy. |
Databáze: | OpenAIRE |
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