» Articles » PMID: 28511503

Evaluation of Total and Lipid Bound Sialic Acid in Serum in Oral Leukoplakia

Overview
Specialty General Medicine
Date 2017 May 18
PMID 28511503
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Oral cancer has become the most common cause of cancer related mortality which may be preceded by oral potentially malignant disorders. Altered glycosylation of glycoconjugates, such as sialic acid are one of the most important molecular changes accompanied during malignant transformation in precancerous lesions like Oral Leukoplakia (OL), and correlating them histopathologically with grades of epithelial dysplasia which will serve clinical significance.

Aim: The aim of this study was to evaluate the significance of serum Total Sialic Acid (TSA) and serum Lipid Bound Sialic Acid (LSA) as a prognostic serum marker in Oral Leukoplakia.

Materials And Methods: Blood samples were collected from 30 patients diagnosed with OL and 30 healthy controls. Serum sialic acid (total and lipid bound) levels were measured using spectrophotometer. Tissue samples were histopathologically typed and were graded for epithelial dysplasia. Data were analysed using Independent t-test and Kruskal Wallis method.

Results: Serum levels of both total and lipid bound sialic acids were found to be increased in OL when compared to healthy controls. The mean TSA levels among those in the OL group (45.3±4.2) were significantly greater than healthy controls (29±2.2). On multiple comparison the highest mean TSA level was found in severe OL compared to moderate and mild OL (p<0.05). The mean levels of LSA were found to be statistically non-significant between the groups.

Conclusion: The present study showed that the serum levels of both TSA and LSA were found to be increased in OL when compared to apparently healthy controls. We also found that with increasing grades of epithelial dysplasia TSA levels were found to be gradually increasing which was significant for this study serving as an early indicator for the detection of malignant transformation in OL.

Citing Articles

Sialic acids in gynecological cancer development and progression: Impact on diagnosis and treatment.

Berghuis A, Pijnenborg J, Boltje T, Pijnenborg J Int J Cancer. 2021; 150(4):678-687.

PMID: 34741527 PMC: 9299683. DOI: 10.1002/ijc.33866.


Serum Sialylation Changes in Actinic Keratosis and Cutaneous Squamous Cell Carcinoma Patients.

Tampa M, Nicolae I, Mitran C, Mitran M, Ene C, Matei C J Pers Med. 2021; 11(10).

PMID: 34683168 PMC: 8538811. DOI: 10.3390/jpm11101027.


Serum sialylation changes in cancer.

Zhang Z, Wuhrer M, Holst S Glycoconj J. 2018; 35(2):139-160.

PMID: 29680984 PMC: 5916985. DOI: 10.1007/s10719-018-9820-0.

References
1.
Rathod S, Khan F, Kolte A, Gupta M . Estimation of salivary and serum total sialic Acid levels in periodontal health and disease. J Clin Diagn Res. 2014; 8(9):ZC19-21. PMC: 4225966. DOI: 10.7860/JCDR/2014/9615.4800. View

2.
Joshi M, Patil R . Estimation and comparative study of serum total sialic acid levels as tumor markers in oral cancer and precancer. J Cancer Res Ther. 2010; 6(3):263-6. DOI: 10.4103/0973-1482.73339. View

3.
Raval G, Parekh L, Patel D, Jha F, Sainger R, Patel P . Clinical usefulness of alterations in sialic acid, sialyl transferase and sialoproteins in breast cancer. Indian J Clin Biochem. 2012; 19(2):60-71. PMC: 3454218. DOI: 10.1007/BF02894259. View

4.
Lopez Saez J . Evaluation of lipid-bound sialic acid (LSA) as a tumor marker. Int J Biol Markers. 1995; 10(3):174-9. DOI: 10.1177/172460089501000308. View

5.
Nigam P, Narain V, Kumar A . Sialic acid in cardiovascular diseases. Indian J Clin Biochem. 2012; 21(1):54-61. PMC: 3453784. DOI: 10.1007/BF02913067. View