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Review
. 2022 Mar 4:12:848376.
doi: 10.3389/fonc.2022.848376. eCollection 2022.

The Interaction Between Non-Coding RNAs and Calcium Binding Proteins

Affiliations
Review

The Interaction Between Non-Coding RNAs and Calcium Binding Proteins

Soudeh Ghafouri-Fard et al. Front Oncol. .

Abstract

Calcium binding proteins (CBP) are a group of proteins mediating the effects of calcium on cellular functions. These proteins can regulate calcium levels inside the cells and contribute in several cellular functions through transporting this ion across cell membranes or decoding related signals. Recent studies have shown that several non-coding RNAs interact with CBPs to affect their expression or activity. The interactions between these transcripts and CBPs have implications in the pathoetiology of human disorders, including both neoplastic and non-neoplastic conditions. In the current review, we describe the interactions between three classes of non-coding RNAs (long non-coding RNAs, circular RNAs, and microRNAs) and a number of CBPs, particularly CAB39, S100A1, S100A4, S100A7 and S100P. This kind of interaction has been verified in different pathological contexts such as drug-induced cardiotoxicity, osteoblasts cytotoxicity, acute lung injury, myocardial ischemia/reperfusion injury, proliferative diabetic retinopathy, glomerulonephritis, as well as a wide array of neoplastic conditions.

Keywords: calcium binding protein; circRNA; lncRNA; miRNA; non-coding RNA.

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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
The connection between CAB39 and miRNAs, as well as their role in human diseases. Inhibition of miRNA has resulted in increased CAB39 levels and increased activity of AMPK pathway. Cab39 has therefore been found as a miRNAs target, and these miRNAs modulate cardiotoxicity, osteoblasts, cytotoxicity, acute lung damage, chemoresistance, senescence, and cancer development through this RNA.
Figure 2
Figure 2
Interaction between CBPs (CAB39 and S100A4) and lncRNAs/circRNAs with their contribution in human disorders.
Figure 3
Figure 3
The interaction of CBPs (S100A4, S100A7, S100A16, S100A9) with miRNAs.

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References

    1. Yáñez M, Gil-Longo J, Campos-Toimil M. Calcium Binding Proteins. Adv Exp Med Biol (2012) 740:461–82. doi: 10.1007/978-94-007-2888-2_19 - DOI - PubMed
    1. Hiraoki T, Vogel HJ. Structure and Function of Calcium-Binding Proteins. J Cardiovasc Pharmacol (1987) 10:S14–31. doi: 10.1097/00005344-198710001-00004 - DOI - PubMed
    1. Boudeau J, Baas AF, Deak M, Morrice NA, Kieloch A, Schutkowski M, et al. . MO25alpha/beta Interact With STRADalpha/beta Enhancing Their Ability to Bind, Activate and Localize LKB1 in the Cytoplasm. EMBO J (2003) 22(19):5102–14. doi: 10.1093/emboj/cdg490 - DOI - PMC - PubMed
    1. Li J, Wan W, Chen T, Tong S, Jiang X, Liu W. miR-451 Silencing Inhibited Doxorubicin Exposure-Induced Cardiotoxicity in Mice. BioMed Res Int (2019) 2019:E collection. doi: 10.1155/2019/1528278 - DOI - PMC - PubMed
    1. Zhuang Y, Wang S, Fei H, Ji F, Sun P. miR-107 Inhibition Upregulates CAB39 and Activates AMPK-Nrf2 Signaling to Protect Osteoblasts From Dexamethasone-Induced Oxidative Injury and Cytotoxicity. Aging (Albany NY) (2020) 12(12):11754. doi: 10.18632/aging.103341 - DOI - PMC - PubMed