Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 May 24:15:687973.
doi: 10.3389/fnins.2021.687973. eCollection 2021.

Alzheimer's Disease and microRNA-132: A Widespread Pathological Factor and Potential Therapeutic Target

Affiliations
Review

Alzheimer's Disease and microRNA-132: A Widespread Pathological Factor and Potential Therapeutic Target

Meng Zhang et al. Front Neurosci. .

Abstract

Alzheimer's disease (AD) is a common neurodegenerative disease in the elderly and is the most common type of dementia. AD is mostly gradual onset, and involves slow, progressive mental decline, accompanied by personality changes; the incidence of AD gradually increases with age. The etiology of AD is unknown, although it is currently believed to be related to abnormal deposition of amyloid β-protein (Aβ) in the brain, hyperphosphorylation of microtubule-associated protein tau, and the release of various cytokines, complements, activators and chemokines by cells. MicroRNAs (miRNAs) are a class of highly conserved non-coding RNAs that regulate gene expression at the post-transcriptional level, and manipulate the functions of intracellular proteins and physiological processes. Emerging studies have shown that miRNA plays an important role in regulating AD-related genes. MiR-132 is known as "NeurimmiR" due to its involvement in numerous neurophysiological and pathological processes. Accumulating pre-clinical results suggest that miR-132 may be involved in the progression of Aβ and tau pathology. Moreover, clinical studies have indicated that decreased circulating miR-132 levels could be used a potential diagnostic biomarker in AD. Here, we review the pathogenic role of miR-132 activity in AD, and the potential of targeting miR-132 for developing future therapeutic strategies.

Keywords: Alzheimer’s disease; biomarker; miR-132; neuroprotection; pathogenesis.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Proposed molecular targets and clinical application of miR-132 in Alzheimer’s disease.

Similar articles

Cited by

References

    1. Ayaz M., Sadiq A., Junaid M., Ullah F., Subhan F., Ahmed J. (2017). Neuroprotective and anti-aging potentials of essential oils from aromatic and medicinal plants. Front. Aging Neurosci. 9:168. 10.3389/fnagi.2017.00168 - DOI - PMC - PubMed
    1. Barry G., Guennewig B., Fung S., Kaczorowski D., Weickert C. S. (2015). Long non-coding RNA expression during aging in the human subependymal zone. Front. Neurol. 6:45. 10.3389/fneur.2015.00045 - DOI - PMC - PubMed
    1. Baumann V., Winkler J. (2014). miRNA-based therapies: strategies and delivery platforms for oligonucleotide and non-oligonucleotide agents. Future Med. Chem. 6 1967–1984. 10.4155/fmc.14.116 - DOI - PMC - PubMed
    1. Bialas A. R., Stevens B. (2013). TGF-β signaling regulates neuronal C1q expression and developmental synaptic refinement. Nat. Neurosci. 16 1773–1782. 10.1038/nn.3560 - DOI - PMC - PubMed
    1. Bloom G. S. (2014). Amyloid-β and tau: the trigger and bullet in Alzheimer disease pathogenesis. JAMA Neurol. 71 505–508. 10.1001/jamaneurol.2013.5847 - DOI - PubMed

LinkOut - more resources