Department of Genetics, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Pediatric Infections Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sci Rep. 2024 Oct 7;14(1):23363. doi: 10.1038/s41598-024-74138-5.
This study aimed to investigate the activation of error-prone DNA repair pathway in response to Helicobacter pylori infection. Relative changes in the expression levels of genes involved in the non-homologous end-joining pathway (NHEJ) in H. pylori-infected (Cases) and non-infected patients (Controls) with chronic gastritis were measured. A significant increase in the relative expression level of TP53, and significant decrease in the relative transcription of lncRNA LINP1 and XRCC5 were detected in the case group. The transcription of Lig4 and XRCC6 was increased in the case group, which was not statistically significant. The Spearman's Correlation Coefficient analysis showed a significant positive-correlation between the transcriptional levels of LINP1 and XRCC4/XRCC5/Lig4, and between XRCC5 and TP53/Lig4 both in the case and control groups. Moreover, a significant positive correlation between LinP1 and XRCC6 in the case, and a significant positive correlation between XRCC4 and Lig4, and a negative correlation between TP53 and LinP1/XRCC4/XRCC5 in the control group was detected. Although a relative difference was detected in transcriptional levels of the NHEJ gene mediators, downregulation of LinP1 in H. pylori-infected patients proposed the activation of a negative feedback loop, which may interfere with the NHEJ activity at the early stages of gastritis.
本研究旨在探讨幽门螺杆菌感染时易错 DNA 修复途径的激活情况。测量了慢性胃炎感染(病例)和未感染(对照)患者中非同源末端连接途径(NHEJ)相关基因表达水平的相对变化。在病例组中,TP53 的相对表达水平显著增加,lncRNA LINP1 和 XRCC5 的相对转录水平显著降低。Lig4 和 XRCC6 的转录在病例组中增加,但无统计学意义。Spearman 相关系数分析显示,在病例和对照组中,LINP1 和 XRCC4/XRCC5/Lig4 的转录水平之间,以及 XRCC5 和 TP53/Lig4 之间均呈显著正相关。此外,在病例组中,LinP1 和 XRCC6 之间存在显著正相关,在对照组中,XRCC4 和 Lig4 之间存在显著正相关,而 TP53 和 LinP1/XRCC4/XRCC5 之间存在负相关。虽然 NHEJ 基因介质的转录水平存在相对差异,但在幽门螺杆菌感染患者中 LinP1 的下调提示了负反馈环的激活,这可能干扰了胃炎早期的 NHEJ 活性。