| Literature DB >> 34473298 |
Elisa Aquilanti1,2, Lauren Kageler2, Patrick Y Wen1, Matthew Meyerson2,3,4.
Abstract
Glioblastoma is the most common primary malignant brain tumor in adults and it continues to have a dismal prognosis. The development of targeted therapeutics has been particularly challenging, in part due to a limited number of oncogenic mutations and significant intra-tumoral heterogeneity. TERT promoter mutations were first discovered in melanoma and later found to be present in up to 80% of glioblastoma samples. They are also frequent clonal alterations in this tumor. TERT promoter mutations are one of the mechanisms for telomerase reactivation, providing cancers with cellular immortality. Telomerase is a reverse transcriptase ribonucleoprotein complex that maintains telomere length in cells with high proliferative ability. In this article, we present genomic and pre-clinical data that support telomerase as a potential "Achilles' heel" for glioblastoma. We also summarize prior experience with anti-telomerase agents and potential new approaches to tackle this target.Entities:
Keywords: genomic driver; glioblastoma; targeted therapies; telomerase
Mesh:
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Year: 2021 PMID: 34473298 PMCID: PMC8643448 DOI: 10.1093/neuonc/noab203
Source DB: PubMed Journal: Neuro Oncol ISSN: 1522-8517 Impact factor: 13.029