Asian Pacific Journal of Cancer Prevention

  • 제16권7호
  • /
  • Pages.2725-2729
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  • 2015
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  • 1513-7368(pISSN)
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  • 2476-762X(eISSN)
아시아태평양암예방학회 (Asian Pacific Journal of Cancer Prevention)
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S100A12 and RAGE Expression in Human Bladder Transitional Cell Carcinoma: a Role for the Ligand/RAGE Axis in Tumor Progression?

  • Khorramdelazad, Hossein (Molecular Medicine Research Center, Rafsanjan University of Medical Sciences) ;
  • Bagheri, Vahid (Molecular Medicine Research Center, Rafsanjan University of Medical Sciences) ;
  • Hassanshahi, Gholamhossein (Molecular Medicine Research Center, Rafsanjan University of Medical Sciences) ;
  • Karami, Hormoz (Department of Urology, Shahid Rahnemoon Hospital, Shahid Sadoughi University of Medical Sciences and Health Services) ;
  • Moogooei, Mozhgan (Molecular Medicine Research Center, Rafsanjan University of Medical Sciences) ;
  • Zeinali, Masoud (Department of Social Medicine, Faculty of Medicine, Rafsanjan University of Medical Sciences) ;
  • Abedinzadeh, Mehdi (Department of Urology, Shahid Rahnemoon Hospital, Shahid Sadoughi University of Medical Sciences and Health Services)
  • 발행 : 2015.04.14
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초록

Background: Transitional cell carcinoma (TCC) and prostate cancer are the most frequent cancers in the male genitourinary tract. Measurement of biological biomarkers may facilitate clinical monitoring and aid early diagnosis of TCC. The aim of the present investigation was to detect the mRNA levels of S100A12 and RAGE (receptor for advanced glycation end products) in patients suffering from bladder TCC. Materials and Methods: To explore the involvement of S100A12 and RAGE genes, total RNA was harvested from cancer tissues and samples obtained from normal non-tumorized urothelium of the same patients. Quantitative PCR (qPCR) was subsequently employed to determine the mRNA levels of S100A12 and RAGE. Results: The results showed that mRNA expression of S100A12 and RAGE was significantly up-regulated in the cancer tissue. Conclusions: According to the results presented in the current study, mRNA expression of S100A12 and RAGE might be as a useful biomarker for TCC. Therefore, this ligand-receptor axis possibly plays important roles in the development of TCC and may serve either as an early diagnostic marker or as a key factor in monitoring of response to treatment. More research is required concerning inhibition of the S100A12-RAGE axis in different cancer models.

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