Oral squamous cell carcinoma (OSCC) is a common malignant tumor, in the head and neck region with a high incidence and prevalence rate globally. Oral cancer is one of the most deadly and common cancers among men in Asian nations including Bangladesh, India, and Pakistan. Certain viral infections, alcohol, betel quid, areca nut, and tobacco use have all been linked to the development of OSCC. Although the role of hormones and their receptors have been explored in many types of cancers, in OSCC it is still poorly explored. Previous studies have reported that sex hormone androgens and androgen receptors (AR) are involved in growth and progression of breast and prostate cancers. However their role in OSCC remains controversial.
The study aims to understand the expression patterns of the androgen receptor at the transcriptional and translational levels in various grades of patients with OSCC. Further to that the expression of AR changes in response to testosterone was also compared in OSCC parients in relation to healthy population.
After obtaining consent, the participants were divided into four categories: healthy, poorly differentiated (PD), moderately differentiated (MD), and well differentiated (WD) squamous cell carcinoma (SCC). By creating an appropriate questionnaire, the patient's history was acquired. Samples of blood and tissue were obtained and processed, for testosterone level measurement using ELISA and RNA and protein estimation using commercially available kits, respectively. Tissue samples were visualized using H&E staining. We found that PDSCC group has highest expression levels of AR mRNA, followed by MDSCC and WDSCC. AR expression and serum testosterone levels were found to have moderately significant association in all subjects, determined by Spearman’s correlation. All groups showed full length AR expression while the splice variant AR-V7 was detected exclusively in MDSCC and PDSCC. This is suggestive of AR-V7 role in in OSCC progression. Higher levels of serum testosterone in OSCC patients than in healthy people provide an evidence for the carcinogenic potential of AR in OSCC.