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https://doi.org/10.1371/journal.pone.0081348
Title: | Sperm associated antigen 9 plays an important role in bladder transitional cell carcinoma | Authors: | Kanojia D. Garg M. Saini S. Agarwal S. Parashar D. Jagadish N. Seth A. Bhatnagar A. Gupta A. Kumar R. Lohiya N.K. Suri A. |
Keywords: | cancer testis antigen cyclin B cyclin D cyclin dependent kinase 1 cyclin dependent kinase 4 cyclin E protein p16 protein p21 sperm associated antigen 9 unclassified drug adult antigen expression article cancer cell cancer grading cell cycle arrest cell cycle G0 phase cell cycle G1 phase cell invasion cell migration cell proliferation controlled study down regulation female gene expression regulation gene silencing genetic association human human cell human tissue humoral immunity major clinical study male middle aged non muscle invasive bladder cancer transitional cell carcinoma upregulation Adaptor Proteins, Signal Transducing Adult Carcinoma, Transitional Cell Cell Cycle Cell Line, Tumor Cell Proliferation Female Humans Male Middle Aged Tumor Markers, Biological Urinary Bladder Neoplasms |
Issue Date: | 2013 | Citation: | Kanojia D., Garg M., Saini S., Agarwal S., Parashar D., Jagadish N., Seth A., Bhatnagar A., Gupta A., Kumar R., Lohiya N.K., Suri A. (2013). Sperm associated antigen 9 plays an important role in bladder transitional cell carcinoma. PLoS ONE 8 (12) : e81348. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0081348 | Rights: | Attribution 4.0 International | Abstract: | Background: Majority of bladder cancer deaths are caused due to transitional cell carcinoma (TCC) which is the most prevalent and chemoresistant malignancy of urinary bladder. Therefore, we analyzed the role of Sperm associated antigen 9 (SPAG9) in bladder TCC. Methodology and Findings: We examined SPAG9 expression and humoral response in 125 bladder TCC patients. Four bladder cancer cell lines were assessed for SPAG9 expression. In addition, we investigated the effect of SPAG9 ablation on cellular proliferation, cell cycle, migration and invasion in UM-UC-3 bladder cancer cells by employing gene silencing approach. Our SPAG9 gene and protein expression analysis revealed SPAG9 expression in 81% of bladder TCC tissue specimens. High SPAG9 expression (>60% SPAG9 positive cells) was found to be significantly associated with superficial non-muscle invasive stage (P = 0.042) and low grade tumors (P = 0.002) suggesting SPAG9 putative role in early spread and tumorigenesis. Humoral response against SPAG9 was observed in 95% of patients found positive for SPAG9 expression. All four bladder cancer cell lines revealed SPAG9 expression. In addition, SPAG9 gene silencing in UM-UC-3 cells resulted in induction of G 0 -G 1 arrest characterized by up-regulation of p16 and p21 and consequent down-regulation of cyclin E, cyclin D and cyclin B, CDK4 and CDK1. Further, SPAG9 gene silencing also resulted in reduction in cellular growth, and migration and invasion ability of cancer cells in vitro. Conclusions: Collectively, our data in clinical specimens indicated that SPAG9 is potential biomarker and therapeutic target for bladder TCC. © 2013 Kanojia et al. | Source Title: | PLoS ONE | URI: | https://scholarbank.nus.edu.sg/handle/10635/161446 | ISSN: | 1932-6203 | DOI: | 10.1371/journal.pone.0081348 | Rights: | Attribution 4.0 International |
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