Abstract
Post-translational modifications (PTMs) affect nearly all systems of the human body due to their role in protein synthesis and functionality. These reversible and irreversible modifications control the structure, localization, activity, and properties of proteins. For this reason, PTMs are essential in regulating cellular processes and maintaining homeostasis. Diseases such as Alzheimer's, cardiovascular disease, diabetes, cancer, and many others have been linked to dysfunctions of PTMs. Recent research has also shown that irregularities in PTMs can be linked to hearing loss, including age-related hearing loss (ARHL) – the number one communication disorder and one of the top neurodegenerative diseases in our aging population. So far, there has been no FDA approved treatment for ARHL; however, translational studies investigating PTMs involvement in ARHL show promising results. In this review, we summarize key findings for PTMs within the auditory system, the involvement of PTMs with aging and ARHL, and lastly discuss potential treatment options focusing on utilizing PTMs as biomarkers and therapeutic pathway components.
Recommended Citation
P. Bazard and J. Pineros and A. A. Acosta and M. Thivierge and L. R. Paganella and S. Zucker and F. L. Mannering and S. Modukuri and X. Zhu and R. D. Frisina and B. Ding, "Post-Translational Modifications and Age-Related Hearing Loss," Hearing Research, vol. 426, article no. 108625, Elsevier, Dec 2022.
The definitive version is available at https://doi.org/10.1016/j.heares.2022.108625
Department(s)
Chemical and Biochemical Engineering
Keywords and Phrases
Age-related Hearing Loss; Aging; Auditory system; Cochlea; Inner ear; Neurodegenerative disorders; Post-translational modifications
International Standard Serial Number (ISSN)
1878-5891; 0378-5955
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2024 Elsevier, All rights reserved.
Publication Date
01 Dec 2022
PubMed ID
36215796
Comments
National Institutes of Health, Grant P01AG009524