Literature DB >> 29557749

Novel Treatment Strategies for the Nervous System: Circadian Clock Genes, Non-coding RNAs, and Forkhead Transcription Factors.

Kenneth Maiese1.   

Abstract

BACKGROUND: With the global increase in lifespan expectancy, neurodegenerative disorders continue to affect an ever-increasing number of individuals throughout the world. New treatment strategies for neurodegenerative diseases are desperately required given the lack of current treatment modalities.
METHODS: Here, we examine novel strategies for neurodegenerative disorders that include circadian clock genes, non-coding Ribonucleic Acids (RNAs), and the mammalian forkhead transcription factors of the O class (FoxOs).
RESULTS: Circadian clock genes, non-coding RNAs, and FoxOs offer exciting prospects to potentially limit or remove the significant disability and death associated with neurodegenerative disorders. Each of these pathways has an intimate relationship with the programmed death pathways of autophagy and apoptosis and share a common link to the silent mating type information regulation 2 homolog 1 (Saccharomyces cerevisiae) (SIRT1) and the mechanistic target of rapamycin (mTOR). Circadian clock genes are necessary to modulate autophagy, limit cognitive loss, and prevent neuronal injury. Non-coding RNAs can control neuronal stem cell development and neuronal differentiation and offer protection against vascular disease such as atherosclerosis. FoxOs provide exciting prospects to block neuronal apoptotic death and to activate pathways of autophagy to remove toxic accumulations in neurons that can lead to neurodegenerative disorders.
CONCLUSION: Continued work with circadian clock genes, non-coding RNAs, and FoxOs can offer new prospects and hope for the development of vital strategies for the treatment of neurodegenerative diseases. These innovative investigative avenues have the potential to significantly limit disability and death from these devastating disorders. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

Entities:  

Keywords:  Aging; Alzheimer's disease; BMAL1; CLOCK; Cryptochrome; FoxO; Huntington’s disease; Parkinson's disease; REV-ERBα; RORE; RORα; aging-related disorders; apoptosis; autophagy; cell longevity; circadianzzm321990rhythm; circular RNA; clock genes; deoxyribonucleic acid; diabetes mellitus; erythropoietin; forkhead; mechanistic target of rapamycin (mTOR); metabolism; microRNA; mitochondria; non-codingzzm321990RNA; oxidative stress; period (PER); programmed cell death; silent matingzzm321990type information regulation 2 homolog 1 (Saccharomyces cerevisiae) (SIRT1); sirtuin; stem cells; transcription factors; vascularzzm321990disease.

Mesh:

Substances:

Year:  2018        PMID: 29557749      PMCID: PMC6021214          DOI: 10.2174/1567202615666180319151244

Source DB:  PubMed          Journal:  Curr Neurovasc Res        ISSN: 1567-2026            Impact factor:   1.990


  224 in total

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