Investigation of the expression of long non-coding RNA in Parkinson’s disease

IF 1.2 Q4 GENETICS & HEREDITY
Mehrdokht Mazdeh, Mohsen Khosravi Farsani, Alireza Komaki, Mohammad Mehadi Eftkharin
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Abstract

Parkinson’s disease is the second most common age-related neurodegenerative disease after Alzheimer’s. Pathogenic factors in Parkinson’s include inflammation and oxidative stress, which lead to dopaminergic cell apoptosis. The case–control study aims to determine the expression level of long non-coding RNAs (lncRNAs) of the apoptosis pathway in Parkinson’s patients compared to healthy individuals. In the case–control study, 50 patients with Parkinson’s disease were examined, along with 50 healthy individuals matched in age and sex. In both groups, the expression of long non-coding RNAs, including taurine upregulated 1 (TUG1), metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), nuclear-enriched abundant transcript 1 (NEAT1), and growth arrest-specific 5 (GAS5), was compared using real-time polymerase chain reaction (PCR). The ratio of MALAT1, NEAT1, and TUG1 gene expression in the case group was statistically significantly higher than in healthy individuals. The ratio of GAS5 gene expression in people with Parkinson’s disease was lower, with a statistically significant difference. The ratio of HULC gene expression was higher in the case group, but it did not show a statistically significant difference with the control group. The involvement of long lncRNAs that increase apoptosis may play a role in the pathogenesis of the disease, which may be used for identification and therapeutic purposes.
帕金森病中长非编码 RNA 的表达研究
帕金森病是仅次于阿尔茨海默病的第二大常见老年性神经退行性疾病。帕金森病的致病因素包括炎症和氧化应激,它们会导致多巴胺能细胞凋亡。病例对照研究旨在确定帕金森病患者与健康人相比,其细胞凋亡通路中长非编码 RNA(lncRNA)的表达水平。在病例对照研究中,50 名帕金森病患者与 50 名年龄和性别相匹配的健康人接受了检查。利用实时聚合酶链反应(PCR)比较了两组患者体内长非编码 RNA 的表达情况,包括牛磺酸上调 1(TUG1)、转移相关肺腺癌转录本 1(MALAT1)、核富集丰富转录本 1(NEAT1)和生长停滞特异性 5(GAS5)。据统计,病例组的 MALAT1、NEAT1 和 TUG1 基因表达比明显高于健康人。帕金森病患者的 GAS5 基因表达比例较低,差异有统计学意义。病例组的 HULC 基因表达比例较高,但与对照组相比差异无统计学意义。增加细胞凋亡的长lncRNA的参与可能在该病的发病机制中发挥作用,可用于鉴定和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics Medicine-Genetics (clinical)
CiteScore
2.20
自引率
7.70%
发文量
150
审稿时长
18 weeks
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