Your browser doesn't support javascript.
loading
Telomerase Reverse Transcriptase-Promoter Mutation in Young Patients with Bladder Tumors.
Pérez González, Sonia; Heredia-Soto, Victoria; Girón de Francisco, Manuel; Pérez-Fernández, Elia; Casans-Francés, Rubén; Mendiola Sabio, Marta; González-Peramato, Pilar.
Afiliação
  • Pérez González S; Department of Urology, Infanta Leonor University Hospital, 28031 Madrid, Spain.
  • Heredia-Soto V; Translational Oncology Research Laboratory, Hospital La Paz Institute for Health Research (IdiPAZ), 28046 Madrid, Spain.
  • Girón de Francisco M; Center for Biomedical Research in the Cancer Network (CIBERONC), Instituto de Salud Carlos III, 28029 Madrid, Spain.
  • Pérez-Fernández E; Department of Urology, La Paz University Hospital, 28046 Madrid, Spain.
  • Casans-Francés R; Research Unit, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain.
  • Mendiola Sabio M; Department of Anesthesia and Pain Medicine, Infanta Elena University Hospital, 28342 Madrid, Spain.
  • González-Peramato P; Center for Biomedical Research in the Cancer Network (CIBERONC), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Curr Issues Mol Biol ; 46(4): 2845-2855, 2024 Mar 23.
Article em En | MEDLINE | ID: mdl-38666908
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.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article