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Effect of 6-aminonicotinamide on the pentose phosphate pathway: 31P NMR and tumor growth delay studies

✍ Scribed by Jason A. Koutcher; Alan A. Alfieri; Cornelia Matei; Kristen L. Meyer; James C. Street; Daniel S. Martin


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
731 KB
Volume
36
Category
Article
ISSN
0740-3194

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✦ Synopsis


Abstract

6‐aminonicotinamide (6AN) has been shown to enhance radio‐sensitivity in vitro, although previous in vivo studies failed to show an effect. ^31^P NMR spectra were obtained by using a one‐dimensional chemical shift imaging technique on a first generation transplant of the CD8FI spontaneous mammary carcinoma tumor model. Spectra were obtained both before and 10 h after treatment with 6AN (20 mg/kg). Changes in pH, nucleoside triphosphate/inorganic phosphate, and phosphocreatine/inorganic phosphate measured at 10 h post‐6AN were not significant. A new peak was detected 10 h post‐6AN, which was assigned to 6‐phosphogluconate (6PG), indicating inhibition of the pentose phosphate pathway (PPP). Based on the spectral data demonstrating inhibition of the PPP at 10 h post‐6AN, tumor‐bearing mice were irradiated (15 Gy × 3 fractions) on Days 1, 10 or 11, and 21 10 h after administration of 6‐aminonicotinamide (20 mg/kg). Tumor‐bearing mice receiving 6AN alone (20 mg/kg × 3), radiation alone (15 Gy × 3), or saline were also studied. Tumor growth delay studies indicated that 6AN alone induced a small but significant tumor growth delay (4.3 ± 0.8 days). Radiation alone induced a tumor growth delay of 34.5 ± 2.7 days. Treatment with 6AN followed by radiation induced a tumor growth delay of 57.0 ± 3.8 days. This was significantly greater than the TGD values for treatment with 6AN alone or radiation (P < 0.01). No complete regressions were noted after treatment with 6AN or radiation alone. Concomitant therapy with 6AN plus radiation yielded 6/28 complete regressions (21%), which was significantly greater than radiation (P < 0.05) or 6AN alone (P < 0.01) on this mammary carcinoma.