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
. 2023 Oct 19;24(20):15344.
doi: 10.3390/ijms242015344.

"Alphabet" Selenoproteins: Implications in Pathology

Affiliations
Review

"Alphabet" Selenoproteins: Implications in Pathology

Carmen Beatrice Dogaru et al. Int J Mol Sci. .

Abstract

Selenoproteins are a group of proteins containing selenium in the form of selenocysteine (Sec, U) as the 21st amino acid coded in the genetic code. Their synthesis depends on dietary selenium uptake and a common set of cofactors. Selenoproteins accomplish diverse roles in the body and cell processes by acting, for example, as antioxidants, modulators of the immune function, and detoxification agents for heavy metals, other xenobiotics, and key compounds in thyroid hormone metabolism. Although the functions of all this protein family are still unknown, several disorders in their structure, activity, or expression have been described by researchers. They concluded that selenium or cofactors deficiency, on the one hand, or the polymorphism in selenoproteins genes and synthesis, on the other hand, are involved in a large variety of pathological conditions, including type 2 diabetes, cardiovascular, muscular, oncological, hepatic, endocrine, immuno-inflammatory, and neurodegenerative diseases. This review focuses on the specific roles of selenoproteins named after letters of the alphabet in medicine, which are less known than the rest, regarding their implications in the pathological processes of several prevalent diseases and disease prevention.

Keywords: cancer; neurodegeneration; selenium; selenoproteins; type 2 diabetes.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Similar articles

Cited by

References

    1. Stadtman T.C. Selenium biochemistry. Science. 1974;183:915–922. doi: 10.1126/science.183.4128.915. - DOI - PubMed
    1. Labunskyy V.M., Hatfield D.L., Gladyshev V.N. Selenoproteins: Molecular pathways and physiological roles. Physiol. Rev. 2014;94:739–777. doi: 10.1152/physrev.00039.2013. - DOI - PMC - PubMed
    1. Bang J., Huh J.H., Na J.W., Lu Q., Carlson B.A., Tobe R., Tsuji P.A., Gladyshev V.N., Hatfield D.L., Lee B.J. Cell Proliferation and Motility Are Inhibited by G1 Phase Arrest in 15-KDa Selenoprotein-Deficient Chang Liver Cells. Mol. Cells. 2015;38:457–465. doi: 10.14348/molcells.2015.0007. - DOI - PMC - PubMed
    1. Cox A.G., Tsomides A., Kim A.J., Saunders D., Hwang K.L., Evason K.J., Heidel J., Brown K.K., Yuan M., Lien E.C., et al. Selenoprotein H Is an Essential Regulator of Redox Homeostasis That Cooperates with P53 in Development and Tumorigenesis. Proc. Natl. Acad. Sci. USA. 2016;113:E5562–E5571. doi: 10.1073/pnas.1600204113. - DOI - PMC - PubMed
    1. Bertz M., Kühn K., Koeberle S.C., Müller M.F., Hoelzer D., Thies K., Deubel S., Thierbach R., Kipp A.P. Selenoprotein H Controls Cell Cycle Progression and Proliferation of Human Colorectal Cancer Cells. Free Radic. Biol. Med. 2018;127:98–107. doi: 10.1016/j.freeradbiomed.2018.01.010. - DOI - PubMed

Grants and funding

This research received no external funding.
-