Antitumorigenic Effect of Wnt 7a and Fzd 9 in Non-small Cell Lung Cancer Cells Is Mediated through ERK-5-dependent Activation of Peroxisome Proliferator-activated Receptor Î

• Published in: The Journal of biological chemistry Vol. 281; no. 37; pp. 26943 - 26950
• Main Authors: Winn, Robert A, Van Scoyk, Michelle, Hammond, Mandy, Rodriguez, Karen, Crossno, Joseph T, Heasley, Lynn E, Nemenoff, Raphael A
• Format: Journal Article
• Language: English
• Published: American Society for Biochemistry and Molecular Biology 15.09.2006
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M604145200

The Wnt pathway is critical for normal development, and mutation of specific components is seen in carcinomas of diverse origins. The role of this pathway in lung tumorigenesis has not been clearly established. Recent studies from our laboratory indicate that combined expression of the combination of Wnt 7a and Frizzled 9 (Fzd 9) in Non-small Cell Lung Cancer (NSCLC) cell lines inhibits transformed growth. We have also shown that increased expression of peroxisome proliferator-activated receptor γ (PPARγ) inhibits transformed growth of NSCLC and promotes epithelial differentiation of these cells. The goal of this study was to determine whether the effects of Wnt 7a/Fzd 9 were mediated through PPARγ. We found that Wnt 7a and Fzd 9 expression led to increased PPARγ activity. This effect was not mediated by altered expression of the protein. Wnt 7a and Fzd 9 expression resulted in activation of ERK5, which was required for PPARγ activation in NSCLC. SR 202, a known PPARγ inhibitor, blocked the increase in PPARγ activity and restored anchorage-independent growth in NSCLC expressing Wnt 7a and Fzd 9. SR 202 also reversed the increase in E-cadherin expression mediated by Wnt 7a and Fzd 9. These data suggest that ERK5-dependent activation of PPARγ represents a major effector pathway mediating the anti-tumorigenic effects of Wnt 7a and Fzd 9 in NSCLC.