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Updated: Nov 10, 2025

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
Published on: June 6, 2017
RNA Helicases as Shadow Modulators of Cell Cycle Progression
Olga Sergeeva1, Timofei Zatsepin1,2
1Skolkovo Institute of Science and Technology, Bolshoy Boulevard 30b1, 121205 Moscow, Russia.
RNA helicases regulate cell cycle progression by modulating transcription and translation of key regulators. Targeting these enzymes may cause side effects due to their broad impact on cell cycle control.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Cell cycle progression relies on cyclins and cyclin-dependent kinases.
- Proteins controlling DNA replication, RNA transcription, and protein synthesis/degradation influence cell cycle regulators.
- RNA helicases are crucial in RNA metabolism, impacting cell cycle regulators at transcriptional and translational levels.
Purpose of the Study:
- To review the direct and indirect roles of RNA helicases in cell cycle regulation.
- To highlight potential downstream effects of RNA helicase inhibition or suppression.
- To inform therapeutic strategies targeting RNA helicases like eIF4A, DDX3, and DDX5.
Main Methods:
- Literature review of studies on RNA helicases and cell cycle control.
- Analysis of RNA helicase involvement in transcription and translation of cell cycle proteins.
- Examination of therapeutic targeting of RNA helicases and associated side effects.
Main Results:
- RNA helicases directly and indirectly influence cell cycle regulators.
- Specific RNA helicases (e.g., eIF4A, DDX3, DDX5) are implicated in cell cycle control.
- Inhibition of RNA helicases can lead to significant side effects due to cell cycle disruption.
Conclusions:
- RNA helicases are critical regulators of the cell cycle through RNA metabolism.
- Understanding the downstream consequences of targeting RNA helicases is essential for safe therapeutic development.
- Further research is needed to balance therapeutic benefits with potential cell cycle-related side effects.
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