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
. 2022 Sep 23;28(1):118.
doi: 10.1186/s10020-022-00546-w.

Targeting miR-21 in spinal cord injuries: a game-changer?

Affiliations
Review

Targeting miR-21 in spinal cord injuries: a game-changer?

Amir Mohammad Malvandi et al. Mol Med. .

Abstract

Spinal cord injury (SCI) is a devastating neurological state causing physical disability, psychological stress and financial burden. SCI global rate is estimated between 250,000 and 500,000 individuals every year, of which 60% of victims are young, healthy males between 15 and 35 years. A variety of pathological conditions such as neuroinflammation, mitochondrial dysfunction, apoptosis, glial scar formation, blood-spinal cord barrier disruption, and angiogenesis disruption occur after SCI leading to a limitation in recovery. MicroRNAs (miRs) are endogenous and non-coding RNAs consisting of 22 nucleotides that regulate 60% of all human genes and involve several normal physiological processes and pathological conditions. miR-21 is among the most highly expressed miRs and its expression has been shown to increase one day after SCI and this elevation is sustained up to 28 days after injury. Overexpression of miR-21 exerts many protective effects against SCI by inhibiting neuroinflammation, improving blood-spinal cord barrier function, regulating angiogenesis, and controlling glial scar formation. It also exhibits anti-apoptotic effects in SCI by down-regulating the expression of PTEN, Spry2, and PDCD4. This review provides a novel therapeutic perspective for miR-21 in SCI.

Keywords: Angiogenesis; Anti-apoptotic; Anti-inflammatory; MicroRNA-21; Neural stem cells; Spinal cord injury.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
miR-21 global molecular mechanism of action leading to functional effects on neural cells’ status and function. ⊥ Represents inhibition, → shows induction/promotion of activity

References

    1. Alizadeh A, Dyck SM, Karimi-Abdolrezaee S. Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Front Neurol. 2019;22(10):282. doi: 10.3389/fneur.2019.00282. - DOI - PMC - PubMed
    1. Anjum A, Yazid MD, Fauzi Daud M, Idris J, Ng AMH, Selvi Naicker A, Ismail OHR, Athi Kumar RK, Lokanathan Y. Spinal cord injury: pathophysiology, multimolecular interactions, and underlying recovery mechanisms. Int J Mol Sci. 2020;21(20):7533. doi: 10.3390/ijms21207533. - DOI - PMC - PubMed
    1. Bao TH, Miao W, Han JH, Yin M, Yan Y, Wang WW, Zhu YH. Spontaneous running wheel improves cognitive functions of mouse associated with miRNA expressional alteration in hippocampus following traumatic brain injury. J Mol Neurosci. 2014;54(4):622–629. doi: 10.1007/s12031-014-0344-1. - DOI - PubMed
    1. Bhalala OG, Pan L, Sahni V, McGuire TL, Gruner K, Tourtellotte WG, Kessler JA. microRNA-21 regulates astrocytic response following spinal cord injury. J Neurosci. 2012;32(50):17935–17947. doi: 10.1523/JNEUROSCI.3860-12.2012. - DOI - PMC - PubMed
    1. Chung HJ, Chung WH, Do SH, Lee JH, Kim HY. Up-regulation of Micrornas-21 and -223 in a Sprague-Dawley Rat model of traumatic spinal cord injury. Brain Sci. 2020;10(3):141. doi: 10.3390/brainsci10030141. - DOI - PMC - PubMed

Publication types