T. Patrice, B. Rozec, A. Sidoroff, Y. Blanloeil, P. Despins, C. Perrigaud
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引用次数: 0
摘要
在非小细胞肺癌中,氧化应激(OS)通过直接氧化其靶细胞或通过产生次级活性氧(SOS)来实现光产生单线态氧(1O2)失活。无论是实验(小鼠原位移植物)还是临床,OS都随进展呈非线性变化。恶病质期OS显著增加,可切除期OS低于对照组。在这两种情况下,它都与较差的预后相关。Vit C或Vit C+GSH在可切除的非小细胞肺癌患者中几乎没有影响,但在对照组中为阴性。Vit E或Vit E + Vit C对NSCLC具有较强的保护作用,其剂量依赖性与病理无关。OS/Vit d呈反比关系,癌症期间的最终辅助补充应以每位患者为基础进行控制。
SECONDARY REACTIVE OXYGEN SPECIES PRODUCTION IN SERA OF PATIENTS WITH RESPECTABLE NON-SQUAMOUS CELL LUNG CANCERS
Oxidative stress (OS) had been evaluated in NSCLC using photoproduced singlet oxygen (1O2) deactivating by oxydizing its targets directly or through secondary reactive oxygen species (SOS) production. Either experimentally (orthotopic grafts in mice) or clinically OS changed non linearly with progression. At time of cachexia OS dramatically increased when at a resectable stage in was lower than in controls.
In both cases it correlated with a worse prognosis. Vit C or Vit C+GSH have nearly no effect in resectable NSCLC patients but a negative one in controls. Vit E or Vit E + Vit C have a stronger protective effect in NSCLC, dose dependent but not related to the pathology. There was a trend to an inverse relationship OS/Vit D. An eventual adjuvant supplementation during cancers should by controlled on a per-patient basis.