Journal
BIOMEDICINES
Volume 10, Issue 3, Pages -Publisher
MDPI
DOI: 10.3390/biomedicines10030564
Keywords
glioblastoma; cell cycle arrest; apoptosis; p53 pathway; Rb pathway; ion channels; nucleocytoplasmic shuttling; Karyopherin a2 (KPNA2); exportin 1 (XPO1)
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Glioblastoma, a common malignant brain tumor, exhibits rapid growth and infiltration. It takes advantage of the patients' biological capacities to maintain its excessive proliferation and invasion, primarily through disrupting cell cycle regulation and apoptosis mechanisms. Molecular targeting therapies have been developed for glioblastoma, and promising therapeutic agents that induce cell cycle arrest and apoptosis are being studied.
Cells of glioblastoma, the most frequent primary malignant brain tumor, are characterized by their rapid growth and infiltration of adjacent healthy brain parenchyma, which reflects their aggressive biological behavior. In order to maintain their excessive proliferation and invasion, glioblastomas exploit the innate biological capacities of the patients suffering from this tumor. The pathways involved in cell cycle regulation and apoptosis are the mechanisms most commonly affected. The following work reviews the regulatory pathways of cell growth in general as well as the dysregulated cell cycle and apoptosis relevant mechanisms observed in glioblastomas. We then describe the molecular targeting of the current established adjuvant therapy and present ongoing trials or completed studies on specific promising therapeutic agents that induce cell cycle arrest and apoptosis of glioblastoma cells.
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