Nrf2-activated expression of sulfiredoxin contributes to urethane-induced lung tumorigenesis. (28th September 2018)

• Record Type: Journal Article
• Authors: Mishra, Murli; Jiang, Hong; Chawsheen, Hedy A.; Gerard, Matthieu; Toledano, Michel B.; Wei, Qiou
• Is Part Of: Cancer letters. Volume 432(2018)
• Page Start: 216
• Page End: 226
• Publication Date: 2018-09-28
• Subjects: Oxidative stress -- Antioxidant -- Signal transduction -- Cell growth and proliferation -- Peroxiredoxins; Srx Sulfiredoxin -- Prx Peroxiredoxin -- Prxs Peroxiredoxins -- AP-1 activator protein 1 -- Nrf2 nuclear related factor 2 -- PBS phosphate buffer saline -- CSC cigarette smoke condensate -- ShNT non-target short hairpin ribonucleic acid -- ShSrx ShRNA targeting Srx -- TUNEL terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2018.06.011
• Languages: English
• ISSNs: 0304-3835

Abstract

Abstract: Lung cancer is the leading cause of cancer death worldwide. Cigarette smoking and exposure to chemical carcinogens are among the risk factors of lung tumorigenesis. In this study, we found that cigarette smoke condensate and urethane significantly stimulated the expression of sulfiredoxin (Srx) at the transcript and protein levels in cultured normal lung epithelial cells, and such stimulation was mediated through the activation of nuclear related factor 2 (Nrf2). To study the role of Srx in lung cancer development in vivo, mice with Srx wildtype, heterozygous or knockout genotype were subjected to the same protocol of urethane treatment to induce lung tumors. By comparing tumor multiplicity and volume between groups of mice with different genotype, we found that Srx knockout mice had a significantly lower number and smaller size of lung tumors. Mechanistically, we demonstrated that loss of Srx led to a decrease of tumor cell proliferation as well as an increase of tumor cell apoptosis. These data suggest that Srx may have an oncogenic role that contributes to the development of lung cancer in smokers or urethane-exposed human subjects. Highlights: Cigarette smoke condensate and urethane activated Srx through the Nrf2-mediated transcription activation. Knockdown of Srx or inhibition of its activity repressed urethane-induced human lung epithelial cell transformation. Srx knockout mice had lower number and smaller size of tumors in urethane-induced lung tumorigenesis. Decreased cell proliferation and increased apoptosis contributed to tumor-resistant phenotype of Srx null mice.