TY - JOUR AU - Wagner, Klaus W. AU - Alam, Hunain AU - Dhar, Shilpa S. AU - Giri, Uma AU - Li, Na AU - Wei, Yongkun AU - Giri, Dipak AU - Cascone, Tina AU - Kim, Jae-Hwan AU - Ye, Yuanqing AU - Multani, Asha S. AU - Chan, Chia-Hsin AU - Erez, Baruch AU - Saigal, Babita AU - Chung, Jimyung AU - Lin, Hui-Kuan AU - Wu, Xifeng AU - Hung, Mien-Chie AU - Heymach, John V. AU - Lee, Min Gyu T1 - KDM2A promotes lung tumorigenesis by epigenetically enhancing ERK1/2 signaling PY - 2013/12/02/ AB - Epigenetic dysregulation has emerged as a major contributor to tumorigenesis. Histone methylation is a well-established mechanism of epigenetic regulation that is dynamically modulated by histone methyltransferases and demethylases. The pathogenic role of histone methylation modifiers in non–small cell lung cancer (NSCLC), which is the leading cause of cancer deaths worldwide, remains largely unknown. Here, we found that the histone H3 lysine 36 (H3K36) demethylase KDM2A (also called FBXL11 and JHDM1A) is frequently overexpressed in NSCLC tumors and cell lines. KDM2A and its catalytic activity were required for in vitro proliferation and invasion of KDM2A-overexpressing NSCLC cells. KDM2A overexpression in NSCLC cells with low KDM2A levels increased cell proliferation and invasiveness. KDM2A knockdown abrogated tumor growth and invasive abilities of NSCLC cells in mouse xenograft models. We identified dual-specificity phosphatase 3 (DUSP3) as a key KDM2A target gene and found that DUSP3 dephosphorylates ERK1/2 in NSCLC cells. KDM2A activated ERK1/2 through epigenetic repression of DUSP3 expression via demethylation of dimethylated H3K36 at the DUSP3 locus. High KDM2A levels correlated with poor prognosis in NSCLC patients. These findings uncover an unexpected role for a histone methylation modifier in activating ERK1/2 in lung tumorigenesis and metastasis, suggesting that KDM2A may be a promising therapeutic target in NSCLC. JF - The Journal of Clinical Investigation JA - J Clin Invest SN - 0021-9738 DO - 10.1172/JCI68642 VL - 123 IS - 12 UR - https://doi.org/10.1172/JCI68642 SP - 5231 EP - 5246 PB - The American Society for Clinical Investigation ER -