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Therapeutic development of polymers for prion disease
Kenta Teruya1, Katsumi Doh-Ura2
1Department of Neurochemistry, Tohoku University Graduate School of Medicine, Seiryo-cho, Aoba-ku, Sendai, 980-8575, Japan.
Cell and Tissue Research
|March 21, 2022
Summary
Polymers show promise in combating prion diseases by targeting abnormal prion protein (PrPSc) accumulation. These compounds offer unique therapeutic strategies and research tools for transmissible spongiform encephalopathies.
Area of Science:
- Neuroscience
- Biochemistry
- Polymer Science
Background:
- Prion diseases, or transmissible spongiform encephalopathies, stem from abnormal prion protein (PrPSc) accumulation in the central nervous system.
- Conventional drug development strategies may be insufficient due to the unique aggregation and structural transformation of prions.
Purpose of the Study:
- To review the historical application of polymers in prion disease research.
- To describe polymers exhibiting anti-prion activity and discuss their common characteristics.
- To highlight the potential of polymers as therapeutic leads and research tools for prion diseases.
Main Methods:
- Overview of historical polymer applications in prion disease research.
- Description and characterization of various polymers with anti-prion activity.
- Discussion of common features among effective anti-prion polymers.
Main Results:
- Numerous compounds, including various polymers, have demonstrated anti-prion activities.
- Polymers present distinct therapeutic strategies beyond conventional methods for prion diseases.
- Polymers are valuable for studying PrPSc structure and developing new anti-prion therapies.
Conclusions:
- Polymers are crucial tools in prion disease research, aiding in understanding PrPSc structure.
- Despite challenges in brain drug delivery, polymers serve as essential leads for developing novel anti-prion therapeutics.
- The unique nature of prions necessitates innovative therapeutic approaches, where polymers play a significant role.

