Mitogen-activated protein kinase kinase-4 promotes cell survival by decreasing PTEN expression through an NFκB-dependent pathway

Dianren Xia, Harish Srinivas, Young Ho Ahn, Gautam Sethi, Xiaoyang Sheng, W. K.Alfred Yung, Qianghua Xia, Paul J. Chiao, Heetae Kim, Powel H. Brown, Ignacio I. Wistuba, Bharat B. Aggarwal, Jonathan M. Kurie

Research output: Contribution to journalArticlepeer-review

93 Scopus citations

Abstract

Mitogen-activated protein kinase kinase-4 (MKK4/SEK1) cooperates with phosphatidylinositol 3-kinase to maintain the survival of non-small cell lung cancer (NSCLC) cells, but the biochemical basis of this phenomenon has not been elucidated. Here we used genetic approaches to modulate MKK4 expression in mouse embryo fibroblasts (MEF cells) and NSCLC cells to identify prosurvival signals downstream of MKK4. Relative to wild-type MEF cells, MKK4-null MEF cells were highly susceptible to apoptosis by LY294002, paclitaxel, or serum starvation. MKK4 promoted the survival of MEF cells by decreasing the expression of phosphatase and tensin homologue deleted from chromosome 10 (PTEN). MKK4 inhibited PTEN transcription by activating NFκB, a transcriptional suppressor of PTEN. MKK4 was required for nuclear translocation of RelA/p65 and processing of the NFκB2 precursor (p100) into the mature form (p52). Studies on a panel of NSCLC cell lines revealed a subset with high MKK4/high NFκB/low PTEN that was relatively resistant to apoptosis. Thus, MKK4 promotes cell survival by activating phosphatidylinositol 3-kinase through an NFκB/PTEN-dependent pathway.

Original languageEnglish
Pages (from-to)3507-3519
Number of pages13
JournalJournal of Biological Chemistry
Volume282
Issue number6
DOIs
StatePublished - 9 Jan 2007

Fingerprint

Dive into the research topics of 'Mitogen-activated protein kinase kinase-4 promotes cell survival by decreasing PTEN expression through an NFκB-dependent pathway'. Together they form a unique fingerprint.

Cite this