Department of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
Department of Pathology, University of Szeged, Szeged, Hungary.
Clin Exp Med. 2024 Aug 14;24(1):192. doi: 10.1007/s10238-024-01464-3.
Telomerase reverse transcriptase promoter (TERTp) mutations are frequently targeted tumor markers, however, they reside in regions with high GC content, which poses challenges when examined with simple molecular techniques or even with next-generation sequencing (NGS). In bladder cancer (BC), TERTp mutations are particularly frequent, however, none of the available tools have demonstrated efficacy in detecting TERTp mutations via a simple noninvasive technique. Therefore, we developed a novel PCR-based method for the detection of the two most common TERTp mutations and demonstrated its use for the analysis of BC samples. The developed SHARD-PCR TERTp mutation detection technique requires PCR and restriction digestion steps that are easily implementable even in less well-equipped laboratories. Cell lines with known mutational status were utilized for method development. Matching urine and tumor tissue samples from BC patients were analyzed, and the results were validated by next-generation sequencing. Analysis of eighteen urine and corresponding tumor tissue samples by SHARD-PCR revealed perfect matches in sample pairs, which paralleled the corresponding NGS results: fourteen samples exhibited mutations at the -124 position, two samples showed mutations at the -146 position, and no mutations were detected in two samples. Our study serves as a proof-of-concept and is limited by its small sample size, nonetheless, it demonstrates that SHARD-PCR is a simple, economic and highly reliable method for detecting TERTp mutations, which are common in different cancer types. For bladder cancer, SHARD-PCR can be performed with the use of noninvasive samples and could replace or complement currently used techniques.
端粒酶逆转录酶启动子 (TERTp) 突变是常见的靶向肿瘤标志物,但它们位于 GC 含量较高的区域,这给简单的分子技术甚至下一代测序 (NGS) 的检测带来了挑战。在膀胱癌 (BC) 中,TERTp 突变尤为常见,但目前尚无可用的工具能够通过简单的非侵入性技术检测 TERTp 突变。因此,我们开发了一种基于 PCR 的新方法来检测两种最常见的 TERTp 突变,并证明其可用于 BC 样本的分析。所开发的 SHARD-PCR TERTp 突变检测技术需要 PCR 和限制性消化步骤,即使在设备较差的实验室也很容易实施。我们利用具有已知突变状态的细胞系来开发该方法。对 BC 患者的尿液和肿瘤组织样本进行了分析,并通过下一代测序对结果进行了验证。通过 SHARD-PCR 对 18 份尿液和相应的肿瘤组织样本进行分析,发现样本对之间完全匹配,与相应的 NGS 结果一致:14 个样本在-124 位有突变,2 个样本在-146 位有突变,2 个样本未检测到突变。我们的研究是一个概念验证,受到样本量小的限制,但它表明 SHARD-PCR 是一种简单、经济且高度可靠的检测 TERTp 突变的方法,这种突变在不同的癌症类型中很常见。对于膀胱癌,SHARD-PCR 可以使用非侵入性样本进行,并且可以替代或补充目前使用的技术。