AI Article Synopsis

  • - Somatic mutations in the TERT promoter are commonly found in urothelial cancer, and detecting these mutations in urine could serve as a promising non-invasive way to identify and monitor the disease.
  • - The study developed highly sensitive droplet digital PCR (ddPCR) assays to effectively detect specific TERT promoter mutations in urine samples, focusing on both common and rare mutations.
  • - The paper outlines a detailed protocol for using ddPCR to screen for these mutations in urine, discusses the limitations of detection for the most frequent mutations, and emphasizes the method's potential benefits for clinical use in urothelial cancer diagnostics.

Article Abstract

Somatic mutations in the telomerase reverse transcriptase (TERT) promoter region are highly frequent in urothelial cancer (UC), and their detection in urine (cell-free DNA from the urine supernatant or DNA from exfoliated cells in the urine pellet) has demonstrated promising evidence as putative non-invasive biomarkers for UC detection and monitoring. However, detecting these tumour-derived mutations in urine requires highly sensitive methods, capable of measuring low-allelic fraction mutations. We developed sensitive droplet digital PCR (ddPCR) assays for detecting urinary TERT promoter mutations (uTERTpm), targeting the two most common mutations (C228T and C250T), as well as the rare A161C, C228A, and CC242-243TT mutations. Here, we described the step-by-step protocol uTERTpm mutation screening using simplex ddPCR assays and give some recommendations for isolation of DNA from urine samples. We also provide limits of detection for the two most frequent mutations and discuss advantages of the method for clinical implementation of the assays for the detection and monitoring of UC.

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Source
http://dx.doi.org/10.1007/978-1-0716-3291-8_13DOI Listing

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