WNT signaling at the intersection between neurogenesis and brain tumorigenesis

被引:24
作者
Alkailani, Maisa I. [1 ]
Aittaleb, Mohamed [1 ]
Tissir, Fadel [1 ,2 ]
机构
[1] Hamad Bin Khalifa Univ, Qatar Fdn, Coll Hlth & Life Sci, Doha, Qatar
[2] Catholic Univ Louvain, Inst Neurosci, Brussels, Belgium
关键词
Wnt/beta-catenin; Wnt/PCP; WNT/calcium; neural progenitor cells; neurogenesis; glioma; glioblastoma therapy; ADULT HIPPOCAMPAL NEUROGENESIS; SMALL-MOLECULE INHIBITOR; CELL POLARITY GENES; NEURAL STEM-CELLS; FACIAL BRANCHIOMOTOR NEURONS; LONG-TERM SURVIVAL; BETA-CATENIN; GLIOBLASTOMA-MULTIFORME; MONOCLONAL-ANTIBODY; IN-VIVO;
D O I
10.3389/fnmol.2022.1017568
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurogenesis and tumorigenesis share signaling molecules/pathways involved in cell proliferation, differentiation, migration, and death. Self-renewal of neural stem cells is a tightly regulated process that secures the accuracy of cell division and eliminates cells that undergo mitotic errors. Abnormalities in the molecular mechanisms controlling this process can trigger aneuploidy and genome instability, leading to neoplastic transformation. Mutations that affect cell adhesion, polarity, or migration enhance the invasive potential and favor the progression of tumors. Here, we review recent evidence of the WNT pathway's involvement in both neurogenesis and tumorigenesis and discuss the experimental progress on therapeutic opportunities targeting components of this pathway.
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页数:17
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