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局部前列腺癌中的胚系 DNA 损伤反应基因突变。

Germline DNA Damage Response Gene Mutations in Localized Prostate Cancer.

机构信息

Clinic of Gastroenterology, Nephro-Urology and Surgery, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, M. K. Ciurlionio St. 21/27, LT-03101 Vilnius, Lithuania.

Laboratory of Genetic Diagnostic, National Cancer Institute, Santariskiu St. 1, LT-08406 Vilnius, Lithuania.

出版信息

Medicina (Kaunas). 2023 Dec 30;60(1):73. doi: 10.3390/medicina60010073.

Abstract

: Germline DNA damage response (DDR) gene mutations correlate with increased prostate cancer (PCa) risk and a more aggressive form of the disease. DDR mutation testing is recommended for metastatic PCa cases, while eligible information about the mutations' burden in the early-stage localized PCa is still limited. This study is aimed at the prospective detection of DDR pathway mutations in cases with localized PCa and correlation with clinical, histopathological, and radiological data. A comparison to the previously assessed cohort of the advanced PCa was performed. : Germline DDR gene mutations were assessed prospectively in DNA samples from 139 patients, using a five-gene panel (, , , , and ) targeted next-generation sequencing. : This study revealed an almost three-fold higher risk of localized PCa among mutation carriers as compared to non-carriers (OR 2.84 and 95% CI: 0.75-20.23, = 0.16). The prevalence of germline DDR gene mutations in PCa cases was 16.8% (18/107) and they were detected only in cases with PI-RADS 4/5 lesions. // mutation carriers were 2.6 times more likely to have a higher (>1) cISUP grade group compared to those with a mutation ( = 0.27). However, the number of cISUP > 1-grade patients with a mutation was significantly higher in advanced PCa than in localized PCa: 66.67% vs. 23.08% ( = 0.047). : The results of our study suggest the potential of genetic screening for selected DDR gene mutations for early identification of cases at risk of aggressive PCa.

摘要

胚系 DNA 损伤反应 (DDR) 基因突变与前列腺癌 (PCa) 风险增加和疾病更具侵袭性的形式相关。DDR 突变检测被推荐用于转移性 PCa 病例,而在早期局限性 PCa 中,有关突变负担的合格信息仍然有限。本研究旨在前瞻性检测局限性 PCa 病例中的 DDR 途径突变,并与临床、组织病理学和影像学数据相关联。并与先前评估的晚期 PCa 队列进行了比较。

前瞻性检测了 139 例患者的 DNA 样本中的 DDR 基因突变,使用了一个靶向下一代测序的五基因 panel(、、、、和)。

这项研究表明,与非携带者相比,突变携带者发生局限性 PCa 的风险几乎高出三倍(OR 2.84 和 95%CI:0.75-20.23, = 0.16)。在 PCa 病例中,胚系 DDR 基因突变的患病率为 16.8%(18/107),仅在 PI-RADS 4/5 病变的病例中检测到。//突变携带者发生 cISUP 分级 > 1 的风险是 突变携带者的 2.6 倍( = 0.27)。然而,在晚期 PCa 中,cISUP > 1 级的 突变患者明显多于局限性 PCa:66.67% vs. 23.08%( = 0.047)。

我们的研究结果表明,对于具有侵袭性 PCa 风险的病例,选择 DDR 基因突变进行遗传筛查具有早期识别的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c1f/10820233/c4c47b97b772/medicina-60-00073-g001.jpg

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