| Literature DB >> 33500708 |
John L Caniglia1, Anvesh Jalasutram1, Swapna Asuthkar1, Joseph Sahagun1, Simon Park1, Aditya Ravindra1, Andrew J Tsung1,2,3, Maheedhara R Guda1, Kiran K Velpula1,2,4.
Abstract
Glioblastoma multiforme (GBM) is the most common malignant brain tumor in adults. With a designation of WHO Grade IV, it is also the most lethal primary brain tumor with a median survival of just 15 months. This is often despite aggressive treatment that includes surgical resection, radiation therapy, and chemotherapy. Based on the poor outcomes and prevalence of the tumor, the demand for innovative therapies continues to represent a pressing issue for clinicians and researchers. In terms of therapies targeting metabolism, the prevalence of the Warburg effect has led to a focus on targeting glucose metabolism to halt tumor progression. While glucose is the dominant source of growth substrate in GBM, a number of unique metabolic pathways are exploited in GBM to meet the increased demand for replication and progression. In this review we aim to explore how metabolites from fatty acid oxidation, the urea cycle, the glutamate-glutamine cycle, and one-carbon metabolism are shunted toward energy producing pathways to meet the high energy demand in GBM. We will also explore how the process of autophagy provides a reservoir of nutrients to support viable tumor cells. By so doing, we aim to establish a foundation of implicated metabolic mechanisms supporting growth and tumorigenesis of GBM within the literature. With the sparse number of therapeutic interventions specifically targeting metabolic pathways in GBM, we hope that this review expands further insight into the development of novel treatment modalities. © The author(s).Entities:
Keywords: arginine; autophagy; fatty acids; glioblastoma; glutamine; metabolism
Year: 2021 PMID: 33500708 PMCID: PMC7797684 DOI: 10.7150/thno.53506
Source DB: PubMed Journal: Theranostics ISSN: 1838-7640 Impact factor: 11.556