Salivary analysis of reactive oxygen species in oral submucous fibrosis and oral squamous cell carcinoma patients

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Research Paper 01/02/2012
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Salivary analysis of reactive oxygen species in oral submucous fibrosis and oral squamous cell carcinoma patients

M. Balasubramanian, S. Chitra
Int. J. Biosci. 2(2), 36-44, February 2012.
Copyright Statement: Copyright 2012; The Author(s).
License: CC BY-NC 4.0

Abstract

In this in vitro study, evaluation of biochemical diagnostic markers like prooxidants, free radicals, total protein content and trace elements has been carried out. Significant elevation in the level of lipid peroxides (p<0.001) in Oral Squamous Cell Carcinoma (OSCC) was found when compared to Oral Sub Mucous Fibrosis (OSMF) patients. Conjugated dienes (p<0.001) were found to be increased in OSMF compared to OSCC patients. There were increased levels of hydroxyl and hydrogen peroxides radicals (p<0.001) in OSMF compared to OSCC patients. An elevated level of trace elements (p<0.001 & p<0.05) was found in OSMF than OSCC patients. High level of zinc & iron (p<0.001) were found in OSCC patients. Total protein content and trace elements alone were found in normal healthy individuals. No detectable amount of prooxidants and free radicals were observed in normal healthy individuals. This shows that the above parameters may be used as good biochemical diagnostic marker for the detection of oral cancer at early stages of cancer development.

Armstrong  D,  Wormer  D,  Dimmitt  S.  1991. Tissue peroxidase in the normal and neoplastic salivary gland. J Clin Lab Anal 5, 293 – 298.

Cederbaum AI, Cohen G. 1984. Methods in Enzymol (Packer, L. Eds). Academic press, San Diego 105, 516 – 522.

Cerutti P, Ghosh R, Oya Y, Austad P. 1994. The role of the cellular defense in oxidant carcinogenesis. Environ Health Perspect 102, 123.

Chessman KH, Slater TF. 1993. An introduction to free radical biochemistry. Br Med Bull 49, 481 – 93.

Chicharro JL, Serrano V, Urena R, Gutierrez AM, Carvajal A, Fernandez – Hernando P, Lucia A. 1999. Trace elements and electrolytes in human resting mixed saliva after exercise. Br J Sports Med 33, 204 – 207.

Copeland BE. 1974. Statistical tools in clinical pathology. In: Davidson I, Heary J B, eds. Clinical Diagnosis by Clinical Philadelphia PA, p. 1 – 14.

Datta K, Sinha S, Chattopadhyay P. 2000. Reactive oxygen species in health and disease. Natl Med J Ind 13, 304 – 310.

David T. Wong D. 2005. M. D., D. Msc., professor and associate dean, research School of Dentistry and Jonson Comprehensive Cancer, University of California, Los Angeles.

Di XC, Schwartz P, Fan Q. 1990. Salivary and serum CA 125 assays for detecting malignant ovarian tumors.

Elaine T. 2003. Introduction  about  protein  level. Verimed Health Network.

Guyton KZ, Kensler TW. 1993. Oxidative mechanisms in carcinogenesis. Br Med Bull 49, 523.

Hilderdrandt AG, Roots I, Tjoe M, Heinemeyer G. 1978. Methods in Enzymol (Fleischer S, Packer L, Eds). Academic press, San Diego 52, 342 – 350.

Irshad M, Chaudhuri PS. 2002. Oxidant – antioxidant system: Role and significance in human body. Indian Journal of Experimental Biology 40, 1233 – 1239.

Klein RA. 1970. The detection of oxidation in liposome preparations. Biochem Biophys Acta 210, 486 – 489.

Lowry OH, Roseborough NJ, Farr AL, Randall RJ. 1951. Protein measurement with Folin phenol reagent. J Biol Chem193, 265.

Nash T. 1953. The colorimetric estimation of formaldehyde by means of the Hantzsch reaction. Biochem J. 55, 416.

Negri L, Pacchioni D, Calabrese F, Giacomasso S, Mastromatto V, Fazio M. 1988. Serum and salivary CEA and GICA levels in oral cavity tumors. Int J Biol Markers 3, 107 – 112.

Ohkawa H, Ohishi N, Yagi K. 1979. Assay for lipid peroxidation in animal tissues by thiobarbituric acid reaction, Anal Biochem 95, 351.

Rucker RB, Romero Chapman N, Wong et al. 1996. Modulation of lysyl oxidase by dietary copper in rats. J Nut. 126, 51 – 60.

Schoneich J. 1967. The induction o chromosomal aberrations by hydrogen peroxide in strains of ascites tumors in mice. Mutation Res 4, 385.

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