| Literature DB >> 25941602 |
Sumit Agarwal1, Deepak Parashar1, Namita Gupta1, Nirmala Jagadish1, Alok Thakar2, Vaishali Suri2, Rajive Kumar3, Anju Gupta4, Abdul S Ansari5, Nirmal Kumar Lohiya5, Anil Suri1.
Abstract
Salivary gland cancers are highly aggressive epithelial tumor associated with metastatic potential and high mortality. The tumors are biologically diverse and are of various histotypes. Besides, the detection and diagnosis is a major problem of salivary gland cancer for available treatment modalities. In the present study, we have investigated the association of sperm associated antigen 9 (SPAG9) expression with salivary gland tumor (SGT). Clinical specimens of benign (n = 16) and malignant tumors (n = 86) were examined for the SPAG9 expression. In addition, the sera and adjacent non-cancerous tissues (n = 72) from available patients were obtained. Our in situ RNA hybridization and immunohistochemistry (IHC) analysis revealed significant difference (p = 0.0001) in SPAG9 gene and protein expression in benign (63%) and malignant tumor (84%) specimens. Further, significant association was also observed between SPAG9 expression and malignant tumors (P = 0.05). A cut-off value of >10% cells expressing SPAG9 protein designated as positive in IHC, predicted presence of malignant SGT with 83.72% sensitivity, 100% specificity, 100% PPV and 83.72% NPV. Humoral response against SPAG9 protein was generated in 68% of SGT patients. A cut-off value of 0.212 OD for anti-SPAG9 antibodies in ELISA predicted presence of malignant SGT with 69.23% sensitivity, 100% specificity, 100% PPV and 78.94% NPV. Collectively, our data suggests that the majority of SGT show significant difference and association among benign and malignant tumors for SPAG9 gene and protein expression and also exhibit humoral response against SPAG9 protein. Hence, SPAG9 may be developed as a biomarker for detection and diagnosis of salivary gland tumors.Entities:
Keywords: SPAG9; biomarker; cancer testis antigen; early detection and diagnosis; immunotherapeutic target
Year: 2014 PMID: 25941602 PMCID: PMC4356038 DOI: 10.4161/2162402X.2014.974382
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110