| Literature DB >> 26461091 |
Sheila R Alcantara Llaguno1, Zilai Wang2, Daochun Sun2, Jian Chen2, Jing Xu2, Euiseok Kim3, Kimmo J Hatanpaa4, Jack M Raisanen4, Dennis K Burns4, Jane E Johnson3, Luis F Parada5.
Abstract
A central question in glioblastoma multiforme (GBM) research is the identity of the tumor-initiating cell, and its contribution to the malignant phenotype and genomic state. We examine the potential of adult lineage-restricted progenitors to induce fully penetrant GBM using CNS progenitor-specific inducible Cre mice to mutate Nf1, Trp53, and Pten. We identify two phenotypically and molecularly distinct GBM subtypes governed by identical driver mutations. We demonstrate that the two subtypes arise from functionally independent pools of adult CNS progenitors. Despite histologic identity as GBM, these tumor types are separable based on the lineage of the tumor-initiating cell. These studies point to the cell of origin as a major determinant of GBM subtype diversity.Entities:
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Year: 2015 PMID: 26461091 PMCID: PMC4607935 DOI: 10.1016/j.ccell.2015.09.007
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743