SIRT5 downregulation is associated with poor prognosis in glioblastoma

X Chen, Z Xu, S Zeng, X Wang, W Liu… - Cancer …, 2019 - content.iospress.com
X Chen, Z Xu, S Zeng, X Wang, W Liu, L Qian, J Wei, X Yang, Q Shen, Z Gong, Y Yan
Cancer Biomarkers, 2019content.iospress.com
OBJECTIVE: Sirtuins (SIRT) are NAD+-dependent protein deacetylases that are involved in
the regulation of cancer-associated pathways. However, the biological role of these
deacetylases remains elusive in glioblastoma (GBM). Here, we evaluated the effects of 7
sirtuins regarding their occurrence and prognostic value for GBM. METHODS: In this
research, the effects of SIRT5 on the occurrence and prognosis of GBM were evaluated
using integrative bioinformatics analyses. RESULTS: Based on comprehensive analyses of …
Abstract
OBJECTIVE:
Sirtuins (SIRT) are NAD+-dependent protein deacetylases that are involved in the regulation of cancer-associated pathways. However, the biological role of these deacetylases remains elusive in glioblastoma (GBM). Here, we evaluated the effects of 7 sirtuins regarding their occurrence and prognostic value for GBM.
METHODS:
In this research, the effects of SIRT5 on the occurrence and prognosis of GBM were evaluated using integrative bioinformatics analyses.
RESULTS:
Based on comprehensive analyses of data obtained from web-based bioinformatics platforms, the data demonstrate that only SIRT5 expression is statistically decreased in GBM tissues. The clinical relevance analysis shows that downregulation of SIRT5 is significantly correlated with a shorter survival time. Moreover, the expression levels of SIRT5 were confirmed to be negatively associated with DNA methylation status. In addition, a protein-protein interaction network was constructed to determine the relationship of genes coexpressed with SIRT5. Functional enrichment analysis revealed that SIRT5 was potentially involved in epithelial-mesenchymal transition and in regulating cell communications.
CONCLUSIONS:
Collectively, our results indicate that SIRT5 acts as a potential suppresser during tumorigenesis, and suggest that SIRT5 may be a promising prognostic biomarker of GBM.
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