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Molecular and clinical characterization of PTRF in glioma via 1,022 samples. | LitMetric

AI Article Synopsis

  • PTRF is involved in gene expression regulation and RNA transcript release, which are linked to various diseases, but its role in glioma is not well understood.
  • Researchers analyzed RNA-sequencing and whole-exome sequencing data to explore PTRF expression characteristics in glioma cases, revealing that high PTRF expression correlates with malignancy and poor prognosis.
  • GO functional enrichment analysis indicated that PTRF is associated with processes like cell migration and angiogenesis, suggesting its potential as a diagnostic and therapeutic target for glioma.

Article Abstract

Polymerase I and transcript release factor (PTRF) plays a role in the regulation of gene expression and the release of RNA transcripts during transcription, which have been associated with various human diseases. However, the role of PTRF in glioma remains unclear. In this study, RNA sequencing (RNA-seq) data (n = 1022 cases) and whole-exome sequencing (WES) data (n = 286 cases) were used to characterize the PTRF expression features. Gene ontology (GO) functional enrichment analysis was used to assess the biological implication of changes in PTRF expression. As a result, the expression of PTRF was associated with malignant progression in gliomas. Meanwhile, somatic mutational profiles and copy number variations (CNV) revealed the glioma subtypes classified by PTRF expression showed distinct genomic alteration. Furthermore, GO functional enrichment analysis suggested that PTRF expression was associated with cell migration and angiogenesis, particularly during an immune response. Survival analysis confirmed that a high expression of PTRF is associated with a poor prognosis. In summary, PTRF may be a valuable factor for the diagnosis and treatment target of glioma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273567PMC
http://dx.doi.org/10.1186/s12885-023-11001-2DOI Listing

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