| Literature DB >> 30293699 |
Francesco Carrozza1, Matteo Santoni2, Francesco Piva3, Liang Cheng4, Antonio Lopez-Beltran5, Marina Scarpelli6, Rodolfo Montironi6, Nicola Battelli7, Stefano Tamberi1.
Abstract
Telomerase activity and telomere length are essential for the pathogenesis of several human diseases, including genitourinary tumors. Telomerase constitutes a complex system that includes human telomerase reverse transcriptase (hTERT), human telomerase RNA component (hTR) and telomerase associated protein 1 (TEP1), which are overexpressed in tumor cells compared to normal cells and are involved in the carcinogenesis and progression of renal cell carcinoma (RCC), bladder (BC) and prostate cancer (PCa). In addition, telomerase degraded peptide fragments expressed on the surface of tumor cells lead to their recognition by immune cells. On this scenario, in vitro and in vivo studies have shown effective anti-tumor activity of hTERT-tailored strategies in genitourinary tumors, including active immunotherapy with hTERT-peptide vaccines and passive immunotherapy with hTERT-transduced T cell infusion. This review emphasizes the role of telomerase in the carcinogenesis and progression of genitourinary tumors, thus underlying the potential of emerging telomerase-tailored immunotherapies in these patients.Entities:
Keywords: Bladder cancer; Immunotherapy; Prostate cancer; Renal cancer; Telomerases
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Year: 2018 PMID: 30293699 DOI: 10.1016/j.critrevonc.2018.07.008
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312