Redox control of senescence and age-related disease
Akshaya Chandrasekaran1, Maria Del Pilar Sosa Idelchik1, J Andrés Melendez1
1SUNY Polytechnic Institute, Colleges of Nanoscale Science and Engineering, 257 Fuller Road, Albany, NY 12203, USA.
Abstract:
The signaling networks that drive the aging process, associated functional deterioration, and pathologies has captured the scientific community's attention for decades. While many theories exist to explain the aging process, the production of reactive oxygen species (ROS) provides a signaling link between engagement of cellular senescence and several age-associated pathologies. Cellular senescence has evolved to restrict tumor progression but the accompanying senescence-associated secretory phenotype (SASP) promotes pathogenic pathways. Here, we review known biological theories of aging and how ROS mechanistically control senescence and the aging process. We also describe the redox-regulated signaling networks controlling the SASP and its important role in driving age-related diseases. Finally, we discuss progress in designing therapeutic strategies that manipulate the cellular redox environment to restrict age-associated pathology.
Insights
Reactive oxygen species (ROS) link cellular senescence and aging pathologies. Manipulating the redox environment offers therapeutic strategies to combat age-related diseases by controlling the senescence-associated secretory phenotype (SASP).
Area of Science:
- Gerontology
- Cellular Biology
- Biochemistry
Background:
- Aging is a complex process involving functional decline and disease.
- Reactive oxygen species (ROS) are implicated in aging and age-related pathologies.
- Cellular senescence, a tumor-suppressive mechanism, contributes to aging via the senescence-associated secretory phenotype (SASP).
Purpose of the Study:
- To review biological theories of aging.
- To elucidate the mechanistic role of ROS in senescence and aging.
- To explore redox-regulated signaling networks controlling SASP and its role in age-related diseases.
- To discuss therapeutic strategies targeting the cellular redox environment.
Main Methods:
- Literature review of aging theories.
- Analysis of ROS-mediated mechanisms in cellular senescence.
- Examination of redox signaling pathways governing SASP.
- Discussion of therapeutic interventions.
Main Results:
- ROS act as a crucial signaling molecule connecting cellular senescence to age-associated pathologies.
- The SASP, regulated by redox signaling, promotes pathogenic pathways contributing to aging.
- Therapeutic manipulation of the cellular redox environment shows promise for restricting age-associated pathology.
Conclusions:
- Understanding ROS and redox signaling is key to deciphering aging mechanisms.
- Targeting cellular senescence and SASP through redox modulation offers a promising therapeutic avenue for age-related diseases.
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