Holeckova Klaudia Hives, Hives Mark, Grendar Marian, Drobkova Henrieta Blahusiak, Kliment Jan
Department of Urology, Jessenius Faculty of Medicine in Martin and University Hospital Martin, Comenius University in Bratislava, Martin, Slovakia.
Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.
In Vivo. 2024 Nov-Dec;38(6):2610-2616. doi: 10.21873/invivo.13737.
BACKGROUND/AIM: This report aimed to present identified variants with pathogenic potential in three genes - TP53, PTEN, and RB1 - in a selected sample of patients with metastatic castration-resistant prostate cancer (mCRPC) with or without the presence of circulating tumor cells (CTCs) and splice variant AR-V7.
Next generation sequencing was performed on an Illumina platform to analyse the genetic profiles of 50 patients with mCRPC. Identified variants were validated using the Integrative Genomic Viewer, and the correlation between these variants and the presence of CTC/AR-V7 was subjected to statistical analysis.
The study revealed a total of 15 genetic alterations in the three examined genes. The presence of rs1042522 (TP53) in mCRPC patients was associated with a significantly reduced likelihood of AR-V7 occurrence (p<0.001), indicating a protective effect. Additionally, patients with AR-V7 showed a marked increase in prostate-specific antigen (PSA) levels. Higher PSA levels were correlated with an increased risk of AR-V7 presence.
The identified genetic mutations and PSA levels have a moderate predictive ability for determining AR-V7 status.
背景/目的:本报告旨在介绍三个基因——TP53、PTEN 和 RB1——中具有潜在致病性的已识别变体,这些变体存在于有或没有循环肿瘤细胞(CTC)和剪接变体 AR-V7 的转移性去势抵抗性前列腺癌(mCRPC)患者的选定样本中。
对 50 名 mCRPC 患者进行了基于 Illumina 平台的下一代测序,以分析其遗传图谱。使用整合基因组浏览器对鉴定出的变体进行验证,并对这些变体与 CTC/AR-V7 的存在进行了统计学分析。
该研究在三个检测基因中共发现了 15 种遗传改变。在 mCRPC 患者中,rs1042522(TP53)的存在与 AR-V7 发生的可能性显著降低(p<0.001)相关,表明存在保护作用。此外,携带 AR-V7 的患者前列腺特异性抗原(PSA)水平显著升高。较高的 PSA 水平与 AR-V7 存在的风险增加相关。
已识别的遗传突变和 PSA 水平对确定 AR-V7 状态具有中等的预测能力。