Telomerase Reverse Transcriptase-Promoter Mutation in Young Patients with Bladder Tumors

Author:

Pérez González Sonia1,Heredia-Soto Victoria23,Girón de Francisco Manuel4,Pérez-Fernández Elia5ORCID,Casans-Francés Rubén6,Mendiola Sabio Marta37,González-Peramato Pilar8910

Affiliation:

1. Department of Urology, Infanta Leonor University Hospital, 28031 Madrid, Spain

2. Translational Oncology Research Laboratory, Hospital La Paz Institute for Health Research (IdiPAZ), 28046 Madrid, Spain

3. Center for Biomedical Research in the Cancer Network (CIBERONC), Instituto de Salud Carlos III, 28029 Madrid, Spain

4. Department of Urology, La Paz University Hospital, 28046 Madrid, Spain

5. Research Unit, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain

6. Department of Anesthesia and Pain Medicine, Infanta Elena University Hospital, 28342 Madrid, Spain

7. Molecular Pathology and Therapeutic Targets Group, Hospital La Paz Institute for Health Research (IdiPAZ), 28046 Madrid, Spain

8. Department of Pathology, La Paz University Hospital, 28046 Madrid, Spain

9. Faculty of Medicine, Universidad Autónoma de Madrid, 28029 Madrid, Spain

10. Cellular Engineering Laboratory, Hospital La Paz Institute for Health Research (IdiPAZ), 28046 Madrid, Spain

Abstract

The TERT (Telomerase Reverse Transcriptase) gene promoter mutation is one of the most prevalent mutations in urothelial bladder tumors and this mutation is related to bladder tumor progression. Our purpose was to evaluate the presence of this mutation in a population of patients who were first diagnosed at age ≤ 40 years and to examine its relationship with tumor characteristics and progression. A molecular study was performed to detect the two most prevalent mutations in the TERT promoter (C228T and C250T). The study included 29 patients, with a mean follow-up of 152 months. There were no statistically significant differences in the clinical or tumor characteristics according to the presence or absence of the mutation. Although the mutation group showed poorer recurrence-free survival (RFS), there was no statistically significant difference and there was no difference in progression-free survival by group (p > 0.05). The pTERT mutations in bladder tumor cells occurred less frequently in younger patients than in older patients, a finding that could indicate different mechanisms of carcinogenesis. The trend towards lower RFS in patients with mutated pTERT needs to be confirmed by further studies, given the small number of patients included in these studies due to the low incidence of bladder tumors in this age group.

Publisher

MDPI AG

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