Abstract
Mutations in the forkhead box O 3a (FOXO3a) gene are closely related to the progression of several types of cancers. However, few studies explore the relationship between FOXO3a and nasopharyngeal carcinoma (NPC). Our findings demonstrate that silencing FOXO3a promotes tumor radioresistance of NPC in vitro and in vivo through inducing EMT and activating Wnt/β-catenin signal pathway. These data establish that FOXO3a can be a novel and reliable NPC marker and a potential therapeutic target against NPC.
Keywords:
Epithelial-mesenchymal transition; FOXO3a; NPC; Radioresistance; Wnt.
Copyright © 2019 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Line, Tumor
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Epithelial-Mesenchymal Transition
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Female
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Forkhead Box Protein O3 / deficiency
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Forkhead Box Protein O3 / genetics
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Forkhead Box Protein O3 / metabolism*
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Gene Knockdown Techniques
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Humans
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Mice
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Mice, Inbred BALB C
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Nasopharyngeal Carcinoma / metabolism*
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Nasopharyngeal Carcinoma / pathology
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Nasopharyngeal Carcinoma / radiotherapy*
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Nasopharyngeal Neoplasms / metabolism*
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Nasopharyngeal Neoplasms / pathology
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Nasopharyngeal Neoplasms / radiotherapy*
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Radiation Tolerance
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Random Allocation
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Wnt Signaling Pathway*
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beta Catenin / metabolism*
Substances
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CTNNB1 protein, human
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FOXO3 protein, human
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Forkhead Box Protein O3
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beta Catenin