Cited by 253Bladder and Urothelial Cancer TreatmentsUrinary and Genital Oncology StudiesCancer Genomics and Diagnostics

TERT Promoter Mutations Occur Early in Urothelial Neoplasia and Are Biomarkers of Early Disease and Disease Recurrence in Urine

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Kinde, Isaac, Munari, Enrico, Faraj, Sheila F., Hruban, Ralph H., Schoenberg, Mark, Bivalacqua, Trinity, Allaf, Mohamad, Springer, Simeon +6 more·2013·Cancer Research

Published version of a preprint

Abstract

Activating mutations occur in the promoter of the telomerase reverse transcriptase (TERT) gene in 66% of muscle-invasive urothelial carcinomas. To explore their role in bladder cancer development and to assess their utility as urine markers for early detection, we sequenced the TERT promoter in 76 well-characterized papillary and flat noninvasive urothelial carcinomas, including 28 pTa low-grade transitional cell carcinomas (TCC), 31 pTa high-grade TCCs, and 17 pTis carcinoma in situ lesions. We also evaluated the sequence of the TERT promoter in a separate series of 14 early bladder neoplasms and matched follow-up urine samples to determine whether urine TERT status was an indicator of disease recurrence. A high rate of TERT promoter mutation was observed in both papillary and flat lesions, as well as in low- and high-grade noninvasive urothelial neoplasms (mean: 74%). In addition, among patients whose tumors harbored TERT promoter mutations, the same mutations were present in follow-up urines in seven of eight patients that recurred but in none of the six patients that did not recur (P < 0.001). TERT promoter mutations occur in both papillary and flat lesions, are the most frequent genetic alterations identified to date in noninvasive precursor lesions of the bladder, are detectable in urine, and seem to be strongly associated with bladder cancer recurrence. These provocative results suggest that TERT promoter mutations may offer a useful urinary biomarker for both early detection and monitoring of bladder neoplasia. Cancer Res; 73(24); 7162–7. ©2013 AACR.

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  • TERT promoter mutations are the most common non-coding mutations in cancer and are found in a growing list of cancers.

    “These mutations are the most common mutations in non-coding sequences in cancer and are found in a long, and almost certainly growing, list of cancers153–158.”

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References 19 · Cited by 253

Authors
Kinde, I., Munari, E., Faraj, S. F., Hruban, R. H., Schoenberg, M., Bivalacqua, T., Allaf, M., Springer, S., Wang, Y., Diaz, L. A., Kinzler, K. W., Vogelstein, B., Papadopoulos, N., & Netto, G. J.
Affiliations
Howard Hughes Medical Institute (US)
Corresponding author
  • Papadopoulos, Nickolas
  • Netto, George J.
Venue
Cancer Research
Published
2013-12-15
Volume
73
Issue
24
Pages
7162-7167
ISSN
  • 0008-5472 (ISSN-L)
  • 1538-7445
OpenAlex
W2106037418
Cited by
253
References
19
Citations by year
2026: 9 · 2025: 10 · 2024: 21 · 2023: 16 · 2022: 14 · 2021: 18 · 2020: 28 · 2019: 22 · 2018: 23 · 2017: 27 · 2016: 23 · 2015: 20 · 2014: 20 · 2013: 2
FWCI
21.34
Type
journal article
Language
en
Open access
Locations
  • Cancer Research (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion)
Funders
  • Howard Hughes Medical Institute
  • National Institutes of Health (n01cn43309-10-0-1, n01cn43302-6-0-1)
  • National Cancer Institute (N01 CN043302, N01 CN043309, CA 152432, P01CA134292, CA 57345, R21CA152432, CA43460, N01 CN43309, R37CA043460, R01CA057345, P01CA077664, N01-CN 43302, P50CA062924, R37CA057345, P30CA006973, CA 62924)
  • National Institute of General Medical Sciences (T32GM007814)
Topics
  • Health Sciences › Medicine › Surgery › Bladder and Urothelial Cancer Treatments
  • Health Sciences › Medicine › Surgery › Urinary and Genital Oncology Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
Keywords
TERT promoter mutation, telomerase reverse transcriptase, urothelial tumors, bladder cancer, urothelial carcinoma, carcinoma in situ, urinary biomarkers, early detection, recurrence, papillary lesions, flat lesions
MeSH terms
Aged, Aged, 80 and over, Urinary Bladder Neoplasms, Female, Humans, Male, Middle Aged, Mutation, Neoplasm Recurrence, Local, Promoter Regions, Genetic, Biomarkers, Tumor, Disease Progression, Telomerase

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