Literature DB >> 24551646

Significance of Serum L-fucose Glycoprotein as Cancer Biomarker in Head and Neck Malignancies without Distant Metastasis.

Rathan K S Shetty1, Satheesh Kumar Bhandary2, Arunava Kali3.   

Abstract

BACKGROUND: Head and neck neoplasia is a major form of cancer in India, accounting for 30% of all cancers which occur in males and 11% of cancers which occur in females. Elevated serum L-fucose glycoprotein levels have been reported to be associated with neoplastic conditions involving various sites. Therefore, monitoring serum/tissue L-fucose glycoprotein levels could be a promising approach for the early diagnosis and prognosis of head neck cancers. AIM: This study was carried out to determine the significance of serum L-fucose levels in head and neck malignancies. SETTINGS AND
DESIGN: This comparative study was carried out at a tertiary care hospital in South India.
MATERIAL AND METHODS: Serum L-fucose glycoprotein levels were estimated in 50 patients with histopathologically confirmed head and neck malignancies and they were compared with those of 50 age- and sex-matched healthy controls. STATISTICAL ANALYSIS USED: Student's t-test was used to compare L-fucose glycoprotein levels in study and control groups.
RESULTS: Most common site of the primary tumour in the current study was oral cavity, followed by larynx, hypopharynx and oropharynx respectively. Comparison of glycoprotein L-fucose in two groups showed more than a two-fold rise in serum fucose levels in cases as compared to the those in controls, with mean values of 11.33±7.39 and 4.74±1.55 mg% in cases and controls respectively. There was no relationship between serum fucose levels and age, sex and tumour differentiation.
CONCLUSION: Serum glycoprotein L-fucose levels can be used as an effective biochemical indicator in conjunction with clinical diagnostic procedures in head and neck neoplasia and they may be useful for monitoring recurrences.

Entities:  

Keywords:  Head and neck neoplasms; Serum L-fucose glycoprotein; Squamous cell carcinoma

Year:  2013        PMID: 24551646      PMCID: PMC3919378          DOI: 10.7860/JCDR/2013/6681.3765

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


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