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1 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: ash.periopg@gmail.com.
2 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: drsheeja@rediffmail.com.
3 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: principaldental@saveetha.com.
4 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: msankari@gmail.com.
1 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: ash.periopg@gmail.com.
2 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: drsheeja@rediffmail.com.
3 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: principaldental@saveetha.com.
4 Department of Periodontics, Saveetha Dental College and Hospitals, 162, Poonamallee High Road, Vellappanchavadi, Chennai, Tamil Nadu 600077, India. Electronic address: msankari@gmail.com.
Sulfiredoxin is a recently discovered member of the oxidoreductases family which plays a crucial role in thiol homoeostasis when under oxidative stress. A myriad of systemic disorders have oxidative stress and reactive oxygen species as the key components in their etiopathogenesis. Recent studies have evaluated the role of this enzyme in oxidative stress mediated diseases such as atherosclerosis, chronic obstructive pulmonary disease and a wide array of carcinomas. Its action is responsible for the normal functioning of cells under oxidative stress and the promotion of cell survival in cancerous cells. This review will highlight the cumulative effects of sulfiredoxin in various systemic disorders with a strong emphasis on its target activity and the factors influencing its expression in such conditions.
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Noh Y.H., Baek J.Y., Jeong W., Rhee S.G., Chang T.S. Sulfiredoxin translocation into mitochondria plays a crucial role in reducing hyperoxidized peroxiredoxin III. Journal of Biological Chemistry. 2009;284:8470–8477. 19176523
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Jönsson T.J., Tsang A.W., Lowther W.T., Furdui C.M. Identification of intact protein thiosulfinate intermediate in the reduction of cysteine sulfinic acid in peroxiredoxin by human sulfiredoxin. Journal of Biological Chemistry. 2008;283:22890–22894. 18593714
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Glauser D.A., Brun T., Gauthier B.R., Schlegel W. Transcriptional response of pancreatic beta cells to metabolic stimulation: large scale identification of immediate-early and secondary response genes. BMC Molecular Biology. 2007;8:54. 17587450
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