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Activation of Keap1/Nrf2 signaling pathway by nuclear epidermal growth factor receptor in cancer cells.
Huo, Longfei; Li, Chia-Wei; Huang, Tzu-Hsuan; Lam, Yung Carmen; Xia, Weiya; Tu, Chun; Chang, Wei-Chao; Hsu, Jennifer L; Lee, Dung-Fang; Nie, Lei; Yamaguchi, Hirohito; Wang, Yan; Lang, Jingyu; Li, Long-Yuan; Chen, Chung-Hsuan; Mishra, Lopa; Hung, Mien-Chie.
Afiliação
  • Huo L; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Li CW; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Huang TH; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Lam YC; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Xia W; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Tu C; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Chang WC; Graduate Institute for Cancer Biology and Center for Molecular Medicine, China Medical University Taichung 404, Taiwan.
  • Hsu JL; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030 ; Graduate Institute for Cancer Biology and Center for Molecular Medicine, China Medical University Taichung 404, Taiwan ; Department of Biotechnology, Asia Uni
  • Lee DF; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Nie L; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Yamaguchi H; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Wang Y; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Lang J; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Li LY; Graduate Institute for Cancer Biology and Center for Molecular Medicine, China Medical University Taichung 404, Taiwan.
  • Chen CH; Genomics Research Center, Academia Sinica Nankang, Taipei 105, Taiwan.
  • Mishra L; Department of Gastroenterology, Hepatology & Nutrition, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030.
  • Hung MC; Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center 1515 Holcombe Boulevard, Houston, TX 77030 ; Graduate Institute for Cancer Biology and Center for Molecular Medicine, China Medical University Taichung 404, Taiwan ; Department of Biotechnology, Asia Uni
Am J Transl Res ; 6(6): 649-63, 2014.
Article em En | MEDLINE | ID: mdl-25628777
ABSTRACT
Nuclear translocation of EGFR has been shown to be important for tumor cell growth, survival, and therapeutic resistance. Previously, we detected the association of EGFR with Keap1 in the nucleus. Keap1 is a Kelch-like ECH-associated protein, which plays an important role in cellular response to chemical and oxidative stress by regulating Nrf2 protein stability and nuclear translocation. In this study, we investigate the role of EGFR in regulating Keap1/Nrf2 cascade in the nucleus and provide evidence to show that nuclear EGFR interacts with and phosphorylates nuclear Keap1 to reduce its nuclear protein level. The reduction of nuclear Keap1 consequently stabilizes nuclear Nrf2 and increases its transcriptional activity in cancer cells, which contributes to tumor cell resistance to chemotherapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transl Res Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Transl Res Ano de publicação: 2014 Tipo de documento: Article