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2000
Volume 21, Issue 10
  • ISSN: 1381-6128
  • E-ISSN: 1873-4286

Abstract

Glioblastoma multiforme (GBM) is one of the most malignant cancers in human brain. The prognosis of GBM is extremely poor because it is resistant to radiotherapy and chemotherapy. Improving understanding of the tumor biology brings some new hope to the treatment of GBM. In this review, we discuss the evidence that FoxM1 promotes the development and progression of GBM by regulating key factors involved in cell proliferation, epithelial to mesenchymal transition (EMT), invasion, angiogenesis and upregulating Wnt/β-catenin signalling. Our recent experimental findings are also summarized to prove that FoxM1 is a novel therapeutic target against GBM.

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/content/journals/cpd/10.2174/1381612821666141211115949
2015-03-01
2024-10-20
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/content/journals/cpd/10.2174/1381612821666141211115949
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  • Article Type: Research Article
Keyword(s): angiogenesis; EMT; FoxM1; Glioblastoma; invasion; tumorigenesis; Wnt/β-catenin signaling
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