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Mechanisms controlling the anti-neoplastic functions of FoxO proteins.
Hou, Tianyun; Li, Zhiming; Zhao, Ying; Zhu, Wei-Guo.
Affiliation
  • Hou T; Guangdong Key Laboratory of Genome Stability and Human Disease Prevention, Department of Biochemistry and Molecular Biology, School of Medicine, Shenzhen University, Shenzhen 518060, China; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing Key Laboratory of
  • Li Z; Guangdong Key Laboratory of Genome Stability and Human Disease Prevention, Department of Biochemistry and Molecular Biology, School of Medicine, Shenzhen University, Shenzhen 518060, China; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing Key Laboratory of
  • Zhao Y; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Peking University Health Science Center, Beiji
  • Zhu WG; Guangdong Key Laboratory of Genome Stability and Human Disease Prevention, Department of Biochemistry and Molecular Biology, School of Medicine, Shenzhen University, Shenzhen 518060, China; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing Key Laboratory of
Semin Cancer Biol ; 50: 101-114, 2018 06.
Article in En | MEDLINE | ID: mdl-29155239
ABSTRACT
The Forkhead box O (FoxO) proteins comprise a family of evolutionarily conserved transcription factors that predominantly function as tumor suppressors. These proteins assume diverse roles in the cellular anti-neoplastic response, including regulation of apoptosis and autophagy, cancer metabolism, cell-cycle arrest, oxidative stress and the DNA damage response. More recently, FoxO proteins have been implicated in cancer immunity and cancer stem-cell (CSC) homeostasis. Interestingly, in some sporadic sub-populations, FoxO protein function may also be manipulated by factors such as ß-catenin whereby they instead can facilitate cancer progression via maintenance of CSC properties or promoting drug resistance or metastasis and invasion. This review highlights the essential biological functions of FoxOs and explores the areas that may be exploited in FoxO protein signaling pathways in the development of novel cancer therapeutic agents.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autophagy / Beta Catenin / Forkhead Transcription Factors / Neoplasms Limits: Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autophagy / Beta Catenin / Forkhead Transcription Factors / Neoplasms Limits: Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2018 Document type: Article