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
. 2024 May;239(5):e31229.
doi: 10.1002/jcp.31229. Epub 2024 Mar 1.

Human antigen R: Exploring its inflammatory response impact and significance in cardiometabolic disorders

Affiliations
Review

Human antigen R: Exploring its inflammatory response impact and significance in cardiometabolic disorders

Shahenda Salah Abdelsam et al. J Cell Physiol. 2024 May.

Abstract

RNA-binding proteins (RBPs) play a crucial role in the regulation of posttranscriptional RNA networks, which can undergo dysregulation in many pathological conditions. Human antigen R (HuR) is a highly researched RBP that plays a crucial role as a posttranscriptional regulator. HuR plays a crucial role in the amplification of inflammatory signals by stabilizing the messenger RNA of diverse inflammatory mediators and key molecular players. The noteworthy correlations between HuR and its target molecules, coupled with the remarkable impacts reported on the pathogenesis and advancement of multiple diseases, position HuR as a promising candidate for therapeutic intervention in diverse inflammatory conditions. This review article examines the significance of HuR as a member of the RBP family, its regulatory mechanisms, and its implications in the pathophysiology of inflammation and cardiometabolic illnesses. Our objective is to illuminate potential directions for future research and drug development by conducting a comprehensive analysis of the existing body of research on HuR.

Keywords: HuR; RNA‐binding proteins (RBPs); abnormal vision Drosophila‐like 1 (ELAVL1); cardiometabolic disease; inflammation.

PubMed Disclaimer

Similar articles

References

REFERENCES

    1. Ahmed, R., Muralidharan, R., Srivastava, A., Johnston, S. E., Zhao, Y. D., Ekmekcioglu, S., Munshi, A., & Ramesh, R. (2021). Molecular targeting of HuR oncoprotein suppresses MITF and induces apoptosis in melanoma cells. Cancers, 13(2), 166. https://doi.org/10.3390/cancers13020166
    1. Al‐Ahmadi, W., Al‐Ghamdi, M., Al‐Haj, L., Al‐Saif, M., & Khabar, K. S. A. (2009). Alternative polyadenylation variants of the RNA binding protein, HuR: Abundance, role of AU‐rich elements and auto‐regulation. Nucleic Acids Research, 37(11), 3612–3624. https://doi.org/10.1093/nar/gkp223
    1. Amadio, M., Bucolo, C., Drago, F., Govoni, S., & Pascale, A. (2009). A new potential pharmacological target in diabetic retinopathy: The HuR pathway. Acta Ophthalmologica, 87(s244). https://doi.org/10.1111/j.1755-3768.2009.219.x
    1. Amadio, M., Bucolo, C., Leggio, G. M., Drago, F., Govoni, S., & Pascale, A. (2010). The PKCβ/HuR/VEGF pathway in diabetic retinopathy. Biochemical Pharmacology, 80(8), 1230–1237. https://doi.org/10.1016/j.bcp.2010.06.033
    1. Amadio, M., Pascale, A., Cupri, S., Pignatello, R., Osera, C., D□Agata, V., D□Amico, A. G., Leggio, G. M., Ruozi, B., Govoni, S., Drago, F., & Bucolo, C. (2016). Nanosystems based on siRNA silencing HuR expression counteract diabetic retinopathy in rat. Pharmacological Research, 111, 713–720. https://doi.org/10.1016/j.phrs.2016.07.042

MeSH terms

LinkOut - more resources