Clinical Study of Aspirin and Zileuton on Biomarkers of Tobacco-Related Carcinogenesis in Current Smokers.
Linda L GarlandJosé Guillen-RodriguezChiu-Hsieh HsuLisa E DavisEva SzaboChristopher R HustedHanqiao LiuAshley LeClercYuriy O AlekseyevHanqiao LiuJulie E BaumanAvrum E SpiraJennifer E Beane-EbelMalgorzata WojtowiczH-H Sherry ChowPublished in: Cancers (2022)
The chemopreventive effect of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) on lung cancer risk is supported by epidemiologic and preclinical studies. Zileuton, a 5-lipoxygenase inhibitor, has additive activity with NSAIDs against tobacco carcinogenesis in preclinical models. We hypothesized that cyclooxygenase plus 5-lipoxygenase inhibition would be more effective than a placebo in modulating the nasal epithelium gene signatures of tobacco exposure and lung cancer. We conducted a randomized, double-blinded study of low-dose aspirin plus zileuton vs. double placebo in current smokers to compare the modulating effects on nasal gene expression and arachidonic acid metabolism. In total, 63 participants took aspirin 81 mg daily plus zileuton (Zyflo CR) 600 mg BID or the placebo for 12 weeks. Nasal brushes from the baseline, end-of-intervention, and one-week post intervention were profiled via microarray. Aspirin plus zilueton had minimal effects on the modulation of the nasal or bronchial gene expression signatures of smoking, lung cancer, and COPD but favorably modulated a bronchial gene expression signature of squamous dysplasia. Aspirin plus zileuton suppressed urinary leukotriene but not prostaglandin E2, suggesting shunting through the cyclooxygenase pathway when combined with 5-lipoxygenase inhibition. Continued investigation of leukotriene inhibitors is needed to confirm these findings, understand the long-term effects on the airway epithelium, and identify the safest, optimally dosed agents.
Keyphrases
- anti inflammatory drugs
- low dose
- gene expression
- dna methylation
- randomized controlled trial
- smoking cessation
- chronic rhinosinusitis
- genome wide
- high dose
- cardiovascular events
- signaling pathway
- double blind
- chronic obstructive pulmonary disease
- stem cells
- physical activity
- high grade
- phase iii
- placebo controlled
- nitric oxide synthase
- cystic fibrosis
- mesenchymal stem cells
- open label
- bone marrow
- nitric oxide
- gestational age