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Glioblastoma stem cell long non-coding RNAs: therapeutic perspectives and opportunities.
Hazra, Rasmani; Debnath, Rinku; Tuppad, Arati.
Affiliation
  • Hazra R; University of New Haven, Biology and Environmental Science Department, West Haven, CT, United States.
  • Debnath R; Department of Biotechnology, Indian Institute of Technology Madras, Chennai, India.
  • Tuppad A; University of New Haven, Biology and Environmental Science Department, West Haven, CT, United States.
Front Genet ; 15: 1416772, 2024.
Article in En | MEDLINE | ID: mdl-39015773
ABSTRACT
Glioblastoma poses a formidable challenge among primary brain tumors its tumorigenic stem cells, capable of self-renewal, proliferation, and differentiation, contribute substantially to tumor initiation and therapy resistance. These glioblastoma stem cells (GSCs), resembling conventional stem and progenitor cells, adopt pathways critical for tissue development and repair, promoting uninterrupted tumor expansion. Long non-coding RNAs (lncRNAs), a substantial component of the human transcriptome, have garnered considerable interest for their pivotal roles in normal physiological processes and cancer pathogenesis. They display cell- or tissue-specific expression patterns, and extensive investigations have highlighted their impact on regulating GSC properties and cellular differentiation, thus offering promising avenues for therapeutic interventions. Consequently, lncRNAs, with their ability to exert regulatory control over tumor initiation and progression, have emerged as promising targets for innovative glioblastoma therapies. This review explores notable examples of GSC-associated lncRNAs and elucidates their functional roles in driving glioblastoma progression. Additionally, we delved deeper into utilizing a 3D in vitro model for investigating GSC biology and elucidated four primary methodologies for targeting lncRNAs as potential therapeutics in managing glioblastoma.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Genet Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Genet Year: 2024 Document type: Article Affiliation country: Country of publication: