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长非编码 RNA-p53 调控网络中遗传变异与缺血性脑卒中预后的关系。

Association Between Genetic Variants in the lncRNA-p53 Regulatory Network and Ischemic Stroke Prognosis.

机构信息

Department of Neurology, The First Affiliated Hospital of China Medical University, Shenyang, 110001, China.

出版信息

Neurotox Res. 2021 Aug;39(4):1171-1180. doi: 10.1007/s12640-021-00357-7. Epub 2021 Apr 2.

Abstract

Long noncoding RNAs (lncRNAs) serve as regulators or effectors of the p53 regulatory pathway. The lncRNA-p53 regulatory network plays an important role in ischemia-induced apoptosis and may be important for post-stroke recovery. Eight genetic variants of p53-related lncRNAs were genotyped in 982 patients to explore the association of single nucleotide polymorphisms (SNPs) in the genes related to the p53 regulatory pathway with ischemic stroke (IS) prognosis in a northern Chinese population. Long- and short-term outcomes were assessed by stroke recurrence and modified Rankin Scale score 3 months after stroke, respectively. We first identified that p53 rs1042522 and LINC-ROR rs2027701 could be associated with IS recurrence risk. On further cumulative effect analysis, we found that these two polymorphisms could jointly be associated with IS recurrence. Patients carrying 2-4 risk alleles showed a significantly higher IS recurrence risk than those harboring no or a single risk allele. In contrast to rs2027701 and rs1042522, the other SNPs were not associated with IS recurrence. Subsequently, we found that TUG1 rs2240183 CC genotype was associated with a favorable IS outcome after adjusting for confounding factors. However, the other seven genetic variants of p53-related lncRNAs were not associated with a functional outcome after stroke. p53 rs1042522 and LINC-ROR rs2027701 may exert combined effects on IS recurrence, and TUG1 rs2240183 may be a new biomarker to predict short-term IS outcomes as it modulates p53-mediated apoptosis.

摘要

长链非编码 RNA(lncRNA)作为 p53 调控途径的调节剂或效应子。lncRNA-p53 调控网络在缺血诱导的细胞凋亡中发挥重要作用,可能对卒中后恢复很重要。在中国北方人群中,我们对 982 例患者的 8 个与 p53 相关的 lncRNA 遗传变异进行了基因分型,以探讨 p53 调控途径相关基因的单核苷酸多态性(SNP)与缺血性卒中(IS)预后的关系。通过卒中复发和卒中后 3 个月改良 Rankin 量表评分评估长短预后。我们首先发现 p53 rs1042522 和 LINC-ROR rs2027701 与 IS 复发风险相关。进一步的累积效应分析发现,这两个多态性可以共同与 IS 复发相关。携带 2-4 个风险等位基因的患者与不携带或仅携带 1 个风险等位基因的患者相比,IS 复发风险显著增加。与 rs2027701 和 rs1042522 不同,其他 SNPs 与 IS 复发无关。随后,我们发现 TUG1 rs2240183 CC 基因型在调整混杂因素后与 IS 预后良好相关。然而,与卒中后功能结局相关的其他七个 p53 相关 lncRNA 的遗传变异没有相关性。p53 rs1042522 和 LINC-ROR rs2027701 可能对 IS 复发有协同作用,TUG1 rs2240183 可能是一个新的预测短期 IS 结局的生物标志物,因为它调节 p53 介导的细胞凋亡。

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