Drug Res (Stuttg) 2014; 64(11): 629-632
DOI: 10.1055/s-0034-1370916
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Antioxidant Enzyme Levels in Pathogenesis of Oral Squamous Cell Carcinoma (OSCC)

W. Huo
1   School of Life Science and Biotechnology, Dalian University of Technology, Dalian, Liaoning, P. R. China
2   Department of Medical Oncology, Dalian Municipal Central Hospital, Dalian, Liaoning, P. R. China
,
Z.-M. Li
2   Department of Medical Oncology, Dalian Municipal Central Hospital, Dalian, Liaoning, P. R. China
,
X.-Y. Pan
2   Department of Medical Oncology, Dalian Municipal Central Hospital, Dalian, Liaoning, P. R. China
,
Y.-M. Bao
1   School of Life Science and Biotechnology, Dalian University of Technology, Dalian, Liaoning, P. R. China
,
L.-J. An
1   School of Life Science and Biotechnology, Dalian University of Technology, Dalian, Liaoning, P. R. China
› Author Affiliations
Further Information

Publication History

received 29 January 2014

accepted 06 February 2014

Publication Date:
12 March 2014 (online)

Abstract

Introduction:

Increased oxidative stress and altered anti-oxidant defense systems have been implicated in the pathogenesis of several diseases including cancer. Therefore, the aim of our study is to evaluate the antioxidant enzyme levels such as superoxide dismutase (SOD) and catalase in blood samples and tissues collected from oral squamous cell carcinoma patients and compared with healthy controls.

Methods:

The collected blood samples and tumor tissues from the diseased individuals and the normal controls are analyzed for malondialdehyde (MDA) and nitric oxide (NO), which is the indicator of oxidative and nitrosative stress respectively. The anti-oxidant enzymes SOD and catalase levels are measured by UV visible spectrophotometer. Subsequently, immuno-histostaining for antioxidant enzymes were performed in oral squamous cell carcinoma biopsies and sections were analyzed.

Results:

The levels of MDA and NO were significantly elevated in the blood and tissue samples of OSCC patients. The antioxidant enzymes SOD and catalase were significantly reduced in OSCC tissues; while in erythrocytes catalase level is reduced whereas the SOD level is increased. Further, the reduced immuno-histostaining was observed for catalase and SOD in OSCC tissues when compared to normal oral epithelium.

Conclusions:

The enhanced levels of MDA and NO revealed that increased oxidative stress in conjunction with the reduced antioxidant defense mechanism in OSCC patients, might be involved in cancer progression. Our results suggest that detection of reactive oxygen species (ROS) and antioxidant enzymes levels might be a valuable marker in cancer prognosis and for improving therapeutic strategies in oral cancer.

 
  • References

  • 1 Topdag S, Aslaner A, Tataroglu C et al. Evaluation of antioxidant capacity in lung carcinoma. Ind J Thorac Cardiovas Surg 2005; 21: 269-271
  • 2 Kolanjiappan K, Ramachandran CR, Manoharan S. Biochemical changes in tumor tissues of oral cancer patients. Clin Biochem 2003; 36: 61-65
  • 3 Yang J, Lam EW, Hammad HM et al. Antioxidant enzyme levels in oral squamous cell carcinoma and normal human oral epithelium. J Oral Pathol Med 2002; 31: 71-77
  • 4 Bahar G, Feinmesser R, Shpitzer T et al. Salivary analysis in oral cancer patients: DNA and protein oxidation, reactive nitrogen species, and antioxidant profile. Cancer 2007; 109: 54-59
  • 5 Beevi SSS, Rasheed AMH, Geetha A. Evaluation of oxidative stress and nitric oxide levels in patients with oral cavity cancer. Jpn J Clin Oncol 2004; 34: 379-385
  • 6 Subapriya R, Kumaraguruparan R, Ramachandran CR et al. Oxidant-antioxidant status in patients with oral squamous cell carcinomas at different intraoral sites. Clin Biochem 2002; 35: 489-493
  • 7 Gokul S, Patil VS, Jailkhani R et al. Oxidant-antioxidant status in blood and tumor tissue of oral squamous cell carcinoma patients. Oral Diseases 2010; 16: 29-33
  • 8 Oberley TD, Oberley LW, Slattery AF et al. Immunohistochemical localization of glutathione-S-transferase and glutathione peroxidase in adult Syrian hamster tissues and during kidney development. Am J Pathol 1991; 139: 355-369
  • 9 Oberley TD, Oberley LW, Slattery AF et al. Immunohistochemical localization of antioxidant enzymes in adult Syrian hamster tissues and during kidney development. Am J Pathol 1990; 137: 199-214
  • 10 Lam EWN, Hammad HM, Zwacka R et al. Immunolocalization and adenoviral vector-mediated manganese superoxide dismutase gene transfer to experimental oral tumors. J Dent Res 2000; 79: 1410-1417
  • 11 Lowry OH, Rosenberg NJ, Farr AL et al. Protein measurement with Folin-phenol reagent. J Biol Chem 1951; 193: 265-275
  • 13 Ohkawa H, Ohisi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979; 95: 351-358
  • 12 Miranda MK, Espey MG, Wink DA. A rapid, simple spectrophotometric method for simultaneous detection of nitrate and nitrite. Nitric Oxide 2001; 5: 62-71
  • 14 Marklund S, Marklund G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974; 47: 469-474
  • 15 Aebi H. Catalase. In: Bergmeyer HU. (ed.) Methods in enzymatic analysis. Vol. 3. Academic Press; New York: 1983: 276-286
  • 16 Manoharan S, Kolanjiappan K, Suresh K et al. Lipid peroxidation & antioxidants status in patients with oral squamous cell carcinoma. Indian J Med Res 2005; 122: 529-534
  • 17 Rasheed MH, Beevi SS, Geetha A. Enhanced lipid peroxidation and nitric oxide products with deranged antioxidant status in patients with head & neck squamous cell carcinoma. Oral Oncol 2007; 43: 333-338
  • 18 Bakan E, Taysi S, Polat MF et al. Nitric oxide levels and lipid peroxidation in plasma of patients with gastric cancer. Jpn J Clin Oncol 2002; 32: 162-166
  • 19 Elchuri S, Oberley TD, Qi W et al. CuZnSOD deficiency leads to persistent and widespread oxidative damage and hepatocarcinogenesis later in life. Oncogene 2005; 24: 367-380
  • 20 Aggarwal S, Subberwal M, Kumar S et al. Brain tumor and role of beta-carotene, a-tocopherol, superoxide dismutase and glutathione peroxidases. J Cancer Res Ther 2006; 2: 24-27
  • 21 Surapaneni KM, Sadagopan C. Status of Lipid peroxidation and antioxidant enzymes in patients with carcinoma of breast. J Med Sci Res 2007; 1: 21-24