缺氧细胞毒素替拉帕嗪诱导肿瘤能量代谢和pH的急性变化:31P磁共振波谱研究。

E O Aboagye, L E Dillehay, Z M Bhujwalla, D J Lee
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引用次数: 10

摘要

替拉帕嗪是一种处于II/III期临床试验的低氧细胞毒素。为了进一步了解其在体内的作用机制,我们检测了替拉帕嗪对肿瘤能量代谢和ph的影响。在C3H小鼠侧翼皮下生长RIF-1和SCCVII肿瘤。采用31P磁共振波谱法(MRS)测定肿瘤能量代谢(以无机磷酸盐与三磷酸核苷酸之比(Pi/NTP)表示)和细胞内pH (pHi)。在RIF-1和SCCVII肿瘤中,0.3 mmol/kg腹腔注射替拉帕嗪后1小时内,Pi/NTP比值分别提高2.6倍和3倍。在RIF-1和SCCVII肿瘤中,pHi分别从7.05+/-0.07下降到6.48+/-0.06,从7.21+/-0.09下降到6.45+/-0.02。肿瘤31P生物能量学和pH的降低是可逆的,以RIF-1肿瘤为例,在5-8小时内Pi/NTP比值进一步增加3.5倍,在24小时时恢复到正常范围。RIF-1肿瘤对应的pHi值在5-8小时为6.88+/-0.05,在24小时为7.16+/-0.05。我们得出结论,替拉帕嗪可引起肿瘤能量代谢和pHi的急性变化。这些发现与合理选择和最佳时机的共给药治疗有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxic cell cytotoxin tirapazamine induces acute changes in tumor energy metabolism and pH: a 31P magnetic resonance spectroscopy study.

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.

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