Abstract
To examine local and systemic oxidative status of lung cancer (LC) and oxidant effects of radiotherapy (RT), this study evaluated antioxidants and markers of oxidative and nitrosative stress in bronchoalveolar lavage (BAL) fluid and in the blood of 36 LC patients and 36 non-cancer controls at baseline and during and after RT for LC. LC patients had higher baseline serum urate, plasma nitrite and lower serum oxidized proteins than controls (p=0.016, p<0.001 and p=0.027, respectively), but BAL fluid oxidative stress markers were similar. RT tended to raise some antioxidants, however, significant increases were seen in serum urate, conjugated dienes and TBARS (p=0.044, p=0.034 and p=0.004, respectively) 3 months after RT. High urate at baseline may compensate against the oxidative stress caused by LC. RT shifts the oxidant/antioxidant balance towards lipid peroxidation, although the antioxidant defense mechanisms of the body appear to counteract the increased oxidative stress rather effectively.
Highlights
Lung cancer (LC) is the leading cause of cancer-related deaths in the Western world [1]
Thirty-six LC patients entered to the study and 36 non-cancer patients served as controls (Table I)
Twenty of the LC patients received radiotherapy, 15 of whom underwent a second bronchoscopy during RT
Summary
Lung cancer (LC) is the leading cause of cancer-related deaths in the Western world [1]. LC is divided into two main groups: non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC). Treatment is based on the staging of the cancer and on the performance status of the patient. Surgery is the main treatment for limited disease. Advanced NSCLC is mainly treated with radiotherapy (RT) and chemoradiotherapy [2Á4]. Radiation generates primary radicals by transferring energy to certain cellular components, e.g. water [5]
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