Malignant Glioma: Lessons from Genomics, Mouse Models, and Stem Cells
Author(s) -
Jian Chen,
Renée M. McKay,
Luis F. Parada
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.03.009
Subject(s) - isocitrate dehydrogenase , biology , glioma , central nervous system , stem cell , somatic evolution in cancer , cancer research , idh1 , cancer , neuroscience , mutation , gene , genetics , biochemistry , enzyme
Eighty percent of malignant tumors that develop in the central nervous system are malignant gliomas, which are essentially incurable. Here, we discuss how recent sequencing studies are identifying unexpected drivers of gliomagenesis, including mutations in isocitrate dehydrogenase 1 and the NF-κB pathway, and how genome-wide analyses are reshaping the classification schemes for tumors and enhancing prognostic value of molecular markers. We discuss the controversies surrounding glioma stem cells and explore how the integration of new molecular data allows for the generation of more informative animal models to advance our knowledge of glioma's origin, progression, and treatment.
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