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Role of Asparagine Endopeptidase in Mediating Wild-Type p53 Inactivation of Glioblastoma.
- Source :
-
JNCI: Journal of the National Cancer Institute . Apr2020, Vol. 112 Issue 4, p343-355. 13p. 4 Color Photographs, 3 Black and White Photographs, 1 Diagram. - Publication Year :
- 2020
-
Abstract
- <bold>Background: </bold>Isocitrate dehydrogenase wild-type (WT) glioblastoma (GBM) accounts for 90% of all GBMs, yet only 27% of isocitrate dehydrogenase WT-GBMs have p53 mutations. However, the tumor surveillance function of WT-p53 in GBM is subverted by mechanisms that are not fully understood.<bold>Methods: </bold>We investigated the proteolytic inactivation of WT-p53 by asparaginyl endopeptidase (AEP) and its effects on GBM progression in cancer cells, murine models, and patients' specimens using biochemical and functional assays. The sera of healthy donors (n = 48) and GBM patients (n = 20) were examined by enzyme-linked immunosorbent assay. Furthermore, effects of AEP inhibitors on GBM progression were evaluated in murine models (n = 6-8 per group). The statistical significance between groups was determined using two-tailed Student t tests.<bold>Results: </bold>We demonstrate that AEP binds to and directly cleaves WT-p53, resulting in the inhibition of WT-p53-mediated tumor suppressor function in both tumor cells and stromal cells via extracellular vesicle communication. High expression of uncleavable p53-N311A-mutant rescue AEP-induced tumorigenesis, proliferation, and anti-apoptotic abilities. Knock down or pharmacological inhibition of AEP reduced tumorigenesis and prolonged survival in murine models. However, overexpression of AEP promoted tumorigenesis and shortened the survival time. Moreover, high AEP levels in GBM tissues were associated with a poor prognosis of GBM patients (n = 83; hazard ratio = 3.94, 95% confidence interval = 1.87 to 8.28; P < .001). A correlation was found between high plasma AEP levels and a larger tumor size in GBM patients (r = 0.6, P = .03), which decreased dramatically after surgery.<bold>Conclusions: </bold>Our results indicate that AEP promotes GBM progression via inactivation of WT-p53 and may serve as a prognostic and therapeutic target for GBM. [ABSTRACT FROM AUTHOR]
- Subjects :
- *GLIOBLASTOMA multiforme
*ASPARAGINE
*VESICLES (Cytology)
*ISOCITRATE dehydrogenase
*ENZYME-linked immunosorbent assay
*KI-67 antigen
*PROTEIN metabolism
*DISEASE progression
*RESEARCH
*XENOGRAFTS
*PROTEASE inhibitors
*ANIMAL experimentation
*RESEARCH methodology
*PROTEOLYTIC enzymes
*GLIOMAS
*EVALUATION research
*MEDICAL cooperation
*COMPARATIVE studies
*CONNECTIVE tissue cells
*CELL lines
*EPITHELIAL cells
*MICE
*PHARMACODYNAMICS
Subjects
Details
- Language :
- English
- ISSN :
- 00278874
- Volume :
- 112
- Issue :
- 4
- Database :
- Academic Search Index
- Journal :
- JNCI: Journal of the National Cancer Institute
- Publication Type :
- Academic Journal
- Accession number :
- 142761031
- Full Text :
- https://doi.org/10.1093/jnci/djz155