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多发性硬化症中的基因表达失调: 和其他候选基因。

Dysregulation of Gene Expressions in Multiple Sclerosis: and Other Candidate Genes.

机构信息

Institute of Biomedical Technologies, National Research Council of Italy, 70126 Bari, Italy.

出版信息

J Integr Neurosci. 2022 Nov 25;22(1):4. doi: 10.31083/j.jin2201004.

Abstract

BACKGROUND

In previous investigations of combined miRNAs/mRNAs expressions in neurodegenerative diseases like Multiple Sclerosis (MS) and Amyotrophic Lateral Sclerosis (ALS) we have targeted some interesting genes and molecular pathways that needed further confirmation.

METHODS

By nanofluidic qPCR analysis, we aimed to verify the expression of genes that resulted differentially expressed in the previous analyses. Data from MS patients - either the pediatric and the adult occurrence of the disease (adMS and pedMS, respectively) - was compared to age-matched healthy groups. As neurological controls we recruited a cohort of ALS subjects, considering published searches of possible genetic similarities between the two diseases.

RESULTS

The main results confirmed the involvement of most of the investigated genes in pedMS and adMS, like and . On the other hand, suggestive MS candidate genes like showed an interesting trend possibly influenced by interfering factors, such as concomitant disease-modifying treatments; it is worth noting that was one of the genes upregulated in ALS compared to age-matched adMS patients, together with the transcription factor .

CONCLUSIONS

Although with caution due to the small sample size, this study confirms the interest in transcriptomic analysis supported by integrated and educated bioinformatics evaluations, to shed further light in complex neurological diseases.

摘要

背景

在之前对多发性硬化症 (MS) 和肌萎缩侧索硬化症 (ALS) 等神经退行性疾病的联合 miRNA/mRNAs 表达的研究中,我们针对了一些有趣的基因和分子途径,这些基因和分子途径需要进一步证实。

方法

通过纳米流体 qPCR 分析,我们旨在验证之前分析中差异表达的基因的表达。将 MS 患者的数据(儿科和成人发病的疾病,分别为 adMS 和 pedMS)与年龄匹配的健康组进行比较。作为神经学对照,我们招募了一组 ALS 患者,考虑到这两种疾病之间可能存在遗传相似性的已发表搜索。

结果

主要结果证实了大多数被研究的基因在 pedMS 和 adMS 中的参与,如 和 。另一方面,像 这样的提示性 MS 候选基因显示出一种有趣的趋势,可能受到干扰因素的影响,例如伴随的疾病修饰治疗;值得注意的是,与年龄匹配的 adMS 患者相比, 在 ALS 中上调,与转录因子 一起。

结论

尽管由于样本量小,需要谨慎,但这项研究证实了对转录组分析的兴趣,支持综合和有教育意义的生物信息学评估,以进一步阐明复杂的神经疾病。

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