Deciphering the relevance of dead box RNA helicases in gliomagenesis and autophagy

Arpit Sharma1, Naveen Soni1, Megha Chaudhary1

  • 1Department of Biochemistry, School of Life Sciences, Central University of Rajasthan, Ajmer, Rajasthan, India.

Human Cell
|November 26, 2025
PubMed

Insights

Dead-box RNA helicases (DDXs) are vital for cell processes and cancer growth. Targeting DDXs and autophagy may offer new glioblastoma treatment strategies.

Area of Science:

  • Molecular Biology
  • Cellular Biology
  • Oncology

Background:

  • Dead-box RNA helicases (DDXs) regulate RNA metabolism, impacting cell functions like translation and ribosome assembly.
  • DDXs are increasingly recognized for their roles in autophagy and oncogenesis, particularly in glioblastoma.
  • Glioblastoma presents significant treatment challenges due to its aggressive nature and resistance to therapies.

Purpose of the Study:

  • To review the multifaceted roles of DDXs in glioblastoma development.
  • To explore the connection between DDX proteins, autophagy, and gliomagenesis.
  • To highlight the therapeutic potential of targeting DDXs and modulating autophagy in glioblastoma.

Main Methods:

  • Literature review of studies on DDXs, autophagy, and glioblastoma.
  • Analysis of DDX involvement in key gliomagenesis pathways.
  • Exploration of therapeutic strategies involving DDX manipulation and autophagy inhibition.

Main Results:

  • DDXs influence critical pathways in gliomagenesis, including cell cycle, EMT, angiogenesis, and immune modulation.
  • DDXs play essential roles in autophagy, a process vital for cellular homeostasis and cancer adaptation.
  • Targeting DDXs could disrupt cancer cell survival mechanisms and impede tumor progression.

Conclusions:

  • DDXs represent a promising therapeutic target in glioblastoma.
  • Modulating autophagy, potentially through DDX inhibition or autophagy inhibitors, may enhance treatment efficacy.
  • Further research is needed to fully elucidate DDX functions and their therapeutic applications in glioblastoma.

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