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Changes in energy metabolism and X-ray sensitivity in murine tumours by the nitric oxide donor SIN-1
P J Wood1, J M Sansom, I J Stratford
1MRC Radiobiology Unit, Chilton, Didcot, Oxon, UK.
Abstract:
The effect of the nitric oxide (NO) donor SIN-1 on energy metabolism was examined in three murine transplantable tumours in vivo using 31P MRS. SIN-1 at 2 mg kg-1 i.v. reduced Pi/total by 40-50% in SCCVII/Ha and KHT tumours within 5 min of injection, returning to control levels by 20 min. However, this dose of SIN-1 did not consistently alter Pi/total in RIF-1 tumours. Reduction in Pi/total in SCCVII/Ha tumours 10 min after 5 mg kg-1 i.v. SIN-1 was similar to that for 2 mg kg-1. SIN-1 at 10 mg kg-1 had no effect on Pi/total at 10 min after injection, but increased this ratio 2-fold over control at 60 min, at which time no effect of the lower doses of SIN-1 were observed. SIN-1 effects on SCCVII/Ha tumour response to X-rays were also examined, using an in vivo/in vitro clonogenic assay 24 h after treatment. SIN-1 at 0.5-2 mg kg-1 i.v. given immediately before irradiation increased tumour cell killing 2-4-fold over that for 15 Gy X-rays alone, while higher SIN-1 doses were ineffective. The results indicate that NO donors can alter tumour energy metabolism and X-ray response in a manner consistent with increased oxygenation. However, these responses are dependent upon dose, timing and tumour type.
Insights
Nitric oxide (NO) donor SIN-1 impacts tumor energy metabolism and X-ray sensitivity. Responses vary with NO donor dose, administration timing, and specific tumor type, suggesting potential for tailored cancer therapies.
Area of Science:
- Biomedical sciences
- Oncology
- Radiotherapy
Background:
- Nitric oxide (NO) plays a complex role in cancer biology.
- Understanding NO donor effects on tumor metabolism and treatment response is crucial for therapeutic development.
Purpose of the Study:
- To investigate the impact of the NO donor SIN-1 on energy metabolism in murine tumors.
- To evaluate the effect of SIN-1 on tumor response to X-ray irradiation in vivo.
Main Methods:
- Utilized 31P magnetic resonance spectroscopy (MRS) to assess energy metabolism in vivo.
- Employed an in vivo/in vitro clonogenic assay to determine tumor cell killing post-irradiation.
Main Results:
- SIN-1 (2 mg/kg) reduced Pi/total ratio in SCCVII/Ha and KHT tumors, but not consistently in RIF-1 tumors.
- Low-dose SIN-1 (0.5-2 mg/kg) given before irradiation enhanced tumor cell killing 2-4 fold.
- Higher SIN-1 doses showed delayed effects on Pi/total or were ineffective in enhancing X-ray response.
Conclusions:
- NO donors like SIN-1 can modulate tumor energy metabolism and radiosensitivity.
- These effects are dependent on the dose of SIN-1, timing of administration, and the specific tumor type.
- Findings suggest NO donors may enhance tumor oxygenation, impacting treatment outcomes.
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