AI Article Synopsis

  • Therapy resistance and recurrence in high-grade gliomas stem from glioma stem cells (GSCs), necessitating a deeper understanding of their molecular characteristics.
  • A study revealed distinct splicing profiles and long non-coding RNA expressions between proneural and mesenchymal GSC subgroups, notably in genes tied to essential cellular functions.
  • The research highlighted specific long non-coding RNAs linked to poor survival in patients with mesenchymal GSCs, suggesting that these differences could explain varying therapeutic responses and cancer traits.

Article Abstract

Therapy resistance and recurrence in high-grade gliomas are driven by their populations of glioma stem cells (GSCs). Thus, detailed molecular characterization of GSCs is needed to develop more effective therapies. We conducted a study to identify differences in the splicing profile and expression of long non-coding RNAs in proneural and mesenchymal GSC cell lines. Genes related to cell cycle, DNA repair, cilium assembly, and splicing showed the most differences between GSC subgroups. We also identified genes distinctly associated with survival among patients of mesenchymal or proneural subgroups. We determined that multiple long non-coding RNAs with increased expression in mesenchymal GSCs are associated with poor survival of glioblastoma patients. In summary, our study established critical differences between proneural and mesenchymal GSCs in splicing profiles and expression of long non-coding RNA. These splicing isoforms and lncRNA signatures may contribute to the uniqueness of GSC subgroups, thus contributing to cancer phenotypes and explaining differences in therapeutic responses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6965107PMC
http://dx.doi.org/10.1038/s41525-019-0108-5DOI Listing

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