| Literature DB >> 26980028 |
Morgan L Cowan1, Simeon Springer2, Doreen Nguyen1, Diana Taheri1, Gunes Guner1, Maria Angelica Mendoza Rodriguez1, Yuxuan Wang3, Isaac Kinde3, Maria Del Carmen Rodriguez Pena1, Christopher J VandenBussche1, Mathew T Olson1, Isabela Cunha4, Kazutoshi Fujita5, Dilek Ertoy6, Kenneth Kinzler2, Trinity Bivalacqua7, Nickolas Papadopoulos2, Bert Vogelstein2, George J Netto8.
Abstract
TERT promoter mutations (TERT-mut) have been detected in 60% to 80% of urothelial carcinomas. A molecular urine-based screening assay for the detection of TERT-mut is currently being pursued by our group and others. A small but significant number of bladder carcinomas are adenocarcinoma. The current study assesses the incidence of TERT-mut in primary adenocarcinomas of urinary bladder. A retrospective search of our institutional pathology records identified 23 cystectomy specimens with a diagnosis of adenocarcinoma (2000-2014). All slides were reviewed by a senior urologic pathologist to confirm tumor type and select a representative formalin-fixed, paraffin-embedded block for mutational analysis. Adequate material for DNA testing was available in 14 cases (7 enteric type and 7 not otherwise specified). TERT-mut sequencing analysis was performed using previously described SafeSeq technique. Overall, 28.5% of primary adenocarcinoma harbored TERT-mut. Interestingly, 57% of nonenteric adenocarcinomas were mutation positive, whereas none of the enteric-type tumors harbored mutations. Similar to urothelial carcinoma, we found a relatively higher rate of TERT-mut among nonenteric-type adenocarcinomas further supporting the potential utility of TERT-mut urine-based screening assay for bladder cancer.Entities:
Keywords: Adenocarcinoma; Bladder carcinoma; Mutation; TERT; Telomerase; Telomerase reverse transcriptase
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Year: 2016 PMID: 26980028 PMCID: PMC5561423 DOI: 10.1016/j.humpath.2016.02.009
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466