Ma LiLi, Liu Yue, Ren Yajing, Mi Na, Fang Jing, Bao Rui, Xu Xiuzhi, Zhang Hongjia, Tang Ying
Department of Neurology, The First Affiliated Hospital of Harbin Medical University, Number 23, You Zheng Street, Nan Gang District, Harbin, 150001, Heilongjiang Province, China.
Department of Neurology, Jilin City Hospital of Chemical Industry, Jilin City, Jilin, China.
Eur J Med Res. 2024 Dec 18;29(1):582. doi: 10.1186/s40001-024-02201-y.
Pyroptosis, a specific type of programmed cell death, which has become a significant factor to Parkinson's disease (PD). Concurrently, long non-coding RNAs (lncRNAs) have garnered attention for their regulatory roles in neurodegenerative disorders. This study was designed to ascertain the key lncRNAs in pyroptosis pathways of PD and elucidate their regulatory mechanisms.
Employing a combination of bioinformatics and machine learning, we analyzed PD data sets GSE133347 and GSE110716. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) recognized different lncRNAs. Through various algorithms such as Least Absolute Shrinkage and Selection Operator (LASSO), Random Forest (RF), and Weighted Gene Co-expression Network Analysis (WGCNA), we recognized LINC01606 and LINC00269, which are key factors during the emergence and development of PD. Furthermore, experimental validation was conducted in PD mouse models to confirm these bioinformatics findings.
The analysis showed that there were a large number of apoptosis-related gene expression changes in Parkinson's syndrome, for example, CASP1 and GSDME were up-regulated, and CASP9 and AIM2 were down-regulated. Among the lncRNAs, LINC01606 and LINC00269 were identified as potential modulators of pyroptosis. Notably, LINC00269 was observed to be significantly downregulated in the brain tissues of a PD mouse model, supporting its involvement in PD. The study also highlighted potential interactions of these lncRNAs with genes like ONECUT2, PRLR, CTNNA3, and LRP2.
This study identifies LINC00269 as a potential contributor to pyroptosis pathways in PD. While further investigation is required to fully elucidate its role, these findings provide new insights into PD pathogenesis and suggest potential avenues for future research on diagnostic and therapeutic targets. The study underscores the importance of integrating bioinformatics with experimental validation in neurodegenerative disease research.
细胞焦亡是一种特定类型的程序性细胞死亡,已成为帕金森病(PD)的一个重要因素。同时,长链非编码RNA(lncRNAs)因其在神经退行性疾病中的调控作用而受到关注。本研究旨在确定PD细胞焦亡途径中的关键lncRNAs,并阐明其调控机制。
我们结合生物信息学和机器学习,分析了PD数据集GSE133347和GSE110716。基因本体论(GO)和京都基因与基因组百科全书(KEGG)识别出不同的lncRNAs。通过最小绝对收缩和选择算子(LASSO)、随机森林(RF)和加权基因共表达网络分析(WGCNA)等各种算法,我们识别出LINC01606和LINC00269,它们是PD发生和发展过程中的关键因素。此外,在PD小鼠模型中进行了实验验证,以证实这些生物信息学研究结果。
分析表明,帕金森综合征中有大量与细胞凋亡相关的基因表达变化,例如,半胱天冬酶1(CASP1)和Gasdermin E(GSDME)上调,而半胱天冬酶9(CASP9)和黑素瘤缺乏因子2(AIM2)下调。在lncRNAs中,LINC01606和LINC00269被确定为细胞焦亡的潜在调节因子。值得注意的是,在PD小鼠模型的脑组织中观察到LINC00269显著下调,支持其与PD有关。该研究还强调了这些lncRNAs与Onecut同源盒2(ONECUT2)、催乳素受体(PRLR)、连环蛋白α3(CTNNA3)和低密度脂蛋白受体相关蛋白2(LRP2)等基因之间的潜在相互作用。
本研究确定LINC00269是PD细胞焦亡途径的一个潜在促成因素。虽然需要进一步研究以充分阐明其作用,但这些发现为PD发病机制提供了新的见解,并为未来诊断和治疗靶点的研究提出了潜在途径。该研究强调了在神经退行性疾病研究中将生物信息学与实验验证相结合的重要性。