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Updated: Nov 25, 2025

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
Published on: September 20, 2018
Regulation of processing bodies: From viruses to cancer epigenetic machinery
Sunmathy Kanakamani1, Padmanaban S Suresh2, Thejaswini Venkatesh1
1Department of Biochemistry and Molecular Biology, Central University of Kerala, Kasargod, India.
Abstract:
Processing bodies (PBs) are 100-300 nm cytoplasmic messenger ribonucleoprotein particle (mRNP) granules that regulate eukaryotic gene expression. These cytoplasmic compartments harbor messenger RNAs (mRNAs) and several proteins involved in mRNA decay, microRNA silencing, nonsense-mediated mRNA decay, and splicing. Though membrane-less, PB structures are maintained by RNA-protein and protein-protein interactions. PB proteins have intrinsically disordered regions and low complexity domains, which account for its liquid to liquid phase separation. In addition to being dynamic and actively involved in the exchange of materials with other mRNPs and organelles, they undergo changes on various cellular cues and environmental stresses, including viral infections. Interestingly, several PB proteins are individually implicated in cancer development, and no study has addressed the effects on PB dynamics after epigenetic modifications of cancer-associated PB genes. In the current review, we summarize modulations undergone by P bodies or P body components upon viral infections. Furthermore, we discuss the selective and widely investigated PB proteins that undergo methylation changes in cancer and their potential as biomarkers.
Insights
Processing bodies (PBs), crucial for gene regulation, change during viral infections. This review explores PB protein methylation in cancer, highlighting their potential as diagnostic biomarkers.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Processing bodies (PBs) are cytoplasmic mRNP granules regulating eukaryotic gene expression.
- PBs are involved in mRNA decay, microRNA silencing, and splicing, maintained by RNA-protein interactions.
- PB dynamics are altered by cellular cues and stresses, including viral infections.
Purpose of the Study:
- To review PB modulations during viral infections.
- To discuss epigenetic modifications, specifically methylation, of PB proteins in cancer.
- To explore the potential of these modified PB proteins as cancer biomarkers.
Main Methods:
- Literature review of studies on PBs, viral infections, and cancer.
- Analysis of research on PB protein function and regulation.
- Examination of epigenetic modifications in cancer-associated PB genes.
Main Results:
- PBs and their components undergo significant changes in response to viral infections.
- Specific PB proteins implicated in cancer development exhibit altered methylation patterns.
- These methylation changes suggest a role for PBs in cancer pathogenesis.
Conclusions:
- PB dynamics are influenced by viral infections, impacting gene expression regulation.
- Methylation of cancer-associated PB proteins represents a potential avenue for cancer biomarker development.
- Further research is warranted to elucidate the precise role of PBs in cancer and their utility as biomarkers.
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