multiomics

多组学
  • 文章类型: Journal Article
    人工智能(AI)有潜力改变心血管实践和研究的各个方面。人工智能技术的指数增长正在定义心血管护理的新领域。有了跨越新诊断模式的创新,新的数字天然疾病生物标志物,以及评估护理质量和预测临床结果的高性能工具。这些数字创新有望扩大心血管筛查和监测的范围,尤其是那些无法获得高质量的人,历史上的专业护理。此外,人工智能正在推动生物和临床发现,这将使未来的心血管护理更加个性化。精确,而且有效。这次审查汇集了这些多样化的人工智能创新,强调临床实践和生物医学发现中多模式心血管人工智能的发展,并设想这个由当代科学和新兴发现支持的新未来。最后,我们定义了关键路径和保障措施,这对于实现这个人工智能未来至关重要,有助于实现所有人的最佳心血管健康和结果。
    Artificial intelligence (AI) has the potential to transform every facet of cardiovascular practice and research. The exponential rise in technology powered by AI is defining new frontiers in cardiovascular care, with innovations that span novel diagnostic modalities, new digital native biomarkers of disease, and high-performing tools evaluating care quality and prognosticating clinical outcomes. These digital innovations promise expanded access to cardiovascular screening and monitoring, especially among those without access to high-quality, specialized care historically. Moreover, AI is propelling biological and clinical discoveries that will make future cardiovascular care more personalized, precise, and effective. The review brings together these diverse AI innovations, highlighting developments in multimodal cardiovascular AI across clinical practice and biomedical discovery, and envisioning this new future backed by contemporary science and emerging discoveries. Finally, we define the critical path and the safeguards essential to realizing this AI-enabled future that helps achieve optimal cardiovascular health and outcomes for all.
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  • 文章类型: Journal Article
    细胞毒性T淋巴细胞相关蛋白4(CTLA4)参与各种癌症的进展,但其在乳腺癌(BRCA)中的生物学作用尚不清楚。因此,我们进行了系统的多体分析,以阐述CTLA4在BRCA中的预后价值和潜在机制。
    我们使用多种生物信息学平台评估了CTLA4表达对BRCA的影响,包括Oncomine,GEPIA,UALCAN,PrognoScan数据库,卡普兰-迈耶绘图仪,R2:Kaplan-Meier扫描仪。
    CTLA4在BRCA肿瘤组织中表达高于正常组织(P<0.01)。BRCA中的CTLA4信使RNA水平基于管腔的BRCA亚型,人表皮生长因子受体2和三阴性BRCA显著高于正常组织(P<0.001)。然而,CTLA4的过度表达与BRCA患者预后较好相关(P<0.001),且与患者年龄等临床病理特征相关,T级,雌激素受体,孕激素受体,和预测分析微阵列50(P<0.01)。多种免疫细胞的浸润与BRCA中CTLA4表达增加有关(P<0.001)。CTLA4在抗原结合方面高度富集,免疫球蛋白复合物,淋巴细胞介导的免疫,和细胞因子-细胞因子受体相互作用。
    这项研究为CTLA4在BRCA中的预后作用提供了暗示性证据,这可能是BRCA的治疗靶标。此外,CTLA4可能通过抗原结合影响BRCA预后,免疫球蛋白复合物,淋巴细胞介导的免疫,和细胞因子-细胞因子受体相互作用。这些发现帮助我们了解CTLA4如何在BRCA中发挥作用,并为更多研究奠定基础。
    UNASSIGNED: The cytotoxic T-lymphocyte-associated protein 4 (CTLA4) is involved in the progression of various cancers, but its biological roles in breast cancer (BRCA) remain unclear. Therefore, we performed a systematic multiomic analysis to expound on the prognostic value and underlying mechanism of CTLA4 in BRCA.
    UNASSIGNED: We assessed the effect of CTLA4 expression on BRCA using a variety of bioinformatics platforms, including Oncomine, GEPIA, UALCAN, PrognoScan database, Kaplan-Meier plotter, and R2: Kaplan-Meier scanner.
    UNASSIGNED: CTLA4 was highly expressed in BRCA tumor tissue compared to normal tissue (P < 0.01). The CTLA4 messenger RNA levels in BRCA based on BRCA subtypes of Luminal, human epidermal growth factor receptor 2, and triple-negative BRCA were considerably higher than in normal tissues (P < 0.001). However, the overexpression of CTLA4 was associated with a better prognosis in BRCA (P < 0.001) and was correlated with clinicopathological characteristics including age, T stage, estrogen receptors, progesterone receptors, and prediction analysis of microarray 50 (P < 0.01). The infiltration of multiple immune cells was associated with increased CTLA4 expression in BRCA (P < 0.001). CTLA4 was highly enriched in antigen binding, immunoglobulin complexes, lymphocyte-mediated immunity, and cytokine-cytokine receptor interaction.
    UNASSIGNED: This study provides suggestive evidence of the prognostic role of CTLA4 in BRCA, which may be a therapeutic target for BRCA. Furthermore, CTLA4 may influence BRCA prognosis through antigen binding, immunoglobulin complexes, lymphocyte-mediated immunity, and cytokine-cytokine receptor interaction. These findings help us understand how CTLA4 plays a role in BRCA and set the stage for more research.
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  • 文章类型: Journal Article
    男性不育是一种生殖障碍,占不孕症的40-50%。目前,在大约70%的不育男性中,原因仍然未知。随着新型组学的引入和高通量技术的进步,潜在的生物标志物正在出现。我们工作的主要目的是概述与特发性男性不育相关的组学方法的不同方面,并突出潜在基因。成绩单,非编码RNA,蛋白质,和代谢物值得进一步探索。使用基因本体论(GO)分析,我们旨在比较来自每种组学方法的丰富的GO术语,并确定它们的重叠。PubMed数据库对2014年2月至2022年6月之间发表的文献进行了筛选,使用关键词:与不同组学方法相关的男性不育:基因组学,表观基因组学,转录组学,ncRNA组学,蛋白质组学,和代谢组学。使用Enrichr工具进行GO富集分析。我们检索了281项全球研究:171项基因组学(DNA水平),21表观基因组学(19个甲基化和两个组蛋白残基修饰),15个转录组学,31个非编码RNA,29蛋白质组学,两种蛋白质翻译后修饰,和19个代谢组学研究。基因本体论比较表明,不同的组学方法导致不同分子因子的鉴定,并且相应的GO术语,从不同的组学方法中获得,不要在更大程度上重叠。随着新的组学水平融入男性不育的特发性原因研究,使用多组学系统生物学方法,我们将更接近找到潜在的生物标志物,从而意识到男性不育的整个范围,他们的事业,预后,潜在的治疗。
    Male infertility is a reproductive disorder, accounting for 40-50% of infertility. Currently, in about 70% of infertile men, the cause remains unknown. With the introduction of novel omics and advancement in high-throughput technology, potential biomarkers are emerging. The main purpose of our work was to overview different aspects of omics approaches in association with idiopathic male infertility and highlight potential genes, transcripts, non-coding RNA, proteins, and metabolites worth further exploring. Using the Gene Ontology (GO) analysis, we aimed to compare enriched GO terms from each omics approach and determine their overlapping. A PubMed database screening for the literature published between February 2014 and June 2022 was performed using the keywords: male infertility in association with different omics approaches: genomics, epigenomics, transcriptomics, ncRNAomics, proteomics, and metabolomics. A GO enrichment analysis was performed using the Enrichr tool. We retrieved 281 global studies: 171 genomics (DNA level), 21 epigenomics (19 of methylation and two histone residue modifications), 15 transcriptomics, 31 non-coding RNA, 29 proteomics, two protein posttranslational modification, and 19 metabolomics studies. Gene ontology comparison showed that different omics approaches lead to the identification of different molecular factors and that the corresponding GO terms, obtained from different omics approaches, do not overlap to a larger extent. With the integration of novel omics levels into the research of idiopathic causes of male infertility, using multi-omic systems biology approaches, we will be closer to finding the potential biomarkers and consequently becoming aware of the entire spectrum of male infertility, their cause, prognosis, and potential treatment.
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  • 文章类型: Journal Article
    基因编辑以增强学习和记忆的神经科学和神经生物学是科学界最感兴趣的。CRISPR系统的进步已经创造了通过从基因和蛋白质的表达到抑制的多种方式来治疗神经系统疾病的途径。神经退行性疾病也被归因于通过控制基因表达影响神经元活性的非规范DNA二级结构。核小体形状,转录,翻译,复制,和重组。本文全面讨论了可能导致神经元命运和功能的DNA调节元件的变化。这项研究展示了CRISPR系统提高学习能力和记忆力的能力,治疗或治愈基于遗传的神经系统疾病,通过DNA操作改变突触间隙神经元的活动和易怒性来缓解精神疾病,而且,使用Cas9的表观遗传修饰。我们探索并研究了每种不同的OMIC技术在改变DNA序列时如何有用。这种对OMIC和细胞行为之间的潜在关系的洞察力使我们通过智能设计和利用CRISPR/Cas9技术来获得更好的神经和精神疗法。
    The neuroscience and neurobiology of gene editing to enhance learning and memory is of paramount interest to the scientific community. The advancements of CRISPR system have created avenues to treat neurological disorders by means of versatile modalities varying from expression to suppression of genes and proteins. Neurodegenerative disorders have also been attributed to non-canonical DNA secondary structures by affecting neuron activity through controlling gene expression, nucleosome shape, transcription, translation, replication, and recombination. Changing DNA regulatory elements which could contribute to the fate and function of neurons are thoroughly discussed in this review. This study presents the ability of CRISPR system to boost learning power and memory, treat or cure genetically-based neurological disorders, and alleviate psychiatric diseases by altering the activity and the irritability of the neurons at the synaptic cleft through DNA manipulation, and also, epigenetic modifications using Cas9. We explore and examine how each different OMIC techniques can come useful when altering DNA sequences. Such insight into the underlying relationship between OMICs and cellular behaviors leads us to better neurological and psychiatric therapeutics by intelligently designing and utilizing the CRISPR/Cas9 technology.
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  • 文章类型: Journal Article
    神经母细胞瘤,与癌症相关的发病率和死亡率很高的儿科恶性肿瘤,对儿科癌症领域具有重要意义。高危NB肿瘤通常是转移性的,存活率低于50%。机器学习方法已被应用于各种神经母细胞瘤患者数据以检索相关的临床和生物学信息并开发预测模型。鉴于这一背景,本研究将对使用机器学习和统计方法分析数据的文献进行分类和总结,组织学切片,和医学图像来进行临床预测。此外,这个问题将被颠倒过来,以及使用机器学习按风险组准确地对NB患者进行分层并预测结果,包括生存和治疗反应,将被总结。总的来说,这项研究旨在对迄今为止在神经母细胞瘤中基于表达的预测模型和机器学习进行的重要工作进行分类和总结,以进行风险分层和患者预后,包括生存,和治疗反应,这可能有助于和指导未来的诊断和治疗工作。
    Neuroblastoma, a paediatric malignancy with high rates of cancer-related morbidity and mortality, is of significant interest to the field of paediatric cancers. High-risk NB tumours are usually metastatic and result in survival rates of less than 50%. Machine learning approaches have been applied to various neuroblastoma patient data to retrieve relevant clinical and biological information and develop predictive models. Given this background, this study will catalogue and summarise the literature that has used machine learning and statistical methods to analyse data such as multi-omics, histological sections, and medical images to make clinical predictions. Furthermore, the question will be turned on its head, and the use of machine learning to accurately stratify NB patients by risk groups and to predict outcomes, including survival and treatment response, will be summarised. Overall, this study aims to catalogue and summarise the important work conducted to date on the subject of expression-based predictor models and machine learning in neuroblastoma for risk stratification and patient outcomes including survival, and treatment response which may assist and direct future diagnostic and therapeutic efforts.
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  • 文章类型: Journal Article
    近年来,塑料污染已成为全球性的环境问题,对农业生态系统和人类健康构成潜在威胁,并可能进一步加剧全球粮食安全问题。研究表明,接触微/纳米塑料(MPs/NPs)可能会导致生理毒性的各个方面,包括植物生物量的减少,细胞内氧化应激爆发,光合作用抑制,减少水分和营养吸收,细胞和遗传毒性,种子萌发阻滞,并且这些影响与MP/NP性质密切相关(类型,颗粒大小,功能组),暴露浓度,暴露持续时间和植物特征(物种,组织,生长阶段)。在简要回顾MPs/NPs对植物生长的生理毒性的基础上,本文从多组学的角度全面综述了MPs/NPs对植物生长的潜在分子机制,包括转录组,代谢组,蛋白质组和微生物组,从而揭示MPs/NPs在植物转录调控中的作用,代谢途径重编程,蛋白质翻译和翻译后修饰,以及根际微生物在多个水平上的重塑。同时,本文还对未来的研究进行了展望,并明确了未来的研究方向和采用的技术。
    In recent years, plastic pollution has become a global environmental problem, posing a potential threat to agricultural ecosystems and human health, and may further exacerbate global food security problems. Studies have revealed that exposure to micro/nano-plastics (MPs/NPs) might cause various aspects of physiological toxicities, including plant biomass reduction, intracellular oxidative stress burst, photosynthesis inhibition, water and nutrient absorption reduction, cellular and genotoxicity, seed germination retardation, and that the effects were closely related to MP/NP properties (type, particle size, functional groups), exposure concentration, exposure duration and plant characteristics (species, tissue, growth stage). Based on a brief review of the physiological toxicity of MPs/NPs to plant growth, this paper comprehensively reviews the potential molecular mechanism of MPs/NPs on plant growth from perspectives of multi-omics, including transcriptome, metabolome, proteome and microbiome, thus to reveal the role of MPs/NPs in plant transcriptional regulation, metabolic pathway reprogramming, protein translational and post-translational modification, as well as rhizosphere microbial remodeling at multiple levels. Meanwhile, this paper also provides prospects for future research, and clarifies the future research directions and the technologies adopted.
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  • 文章类型: Journal Article
    三阴性乳腺癌(TNBC)由于其攻击行为和有限的治疗选择而在肿瘤学中提出了重大挑战。这篇综述探讨了免疫治疗的潜力,特别是基于疫苗的方法,解决TNBC问题。它探讨了免疫信息学在创建针对TNBC的有效疫苗中的作用。该综述首先强调了TNBC的独特属性以及肿瘤抗原在疫苗开发中的重要性。然后阐述了抗原检测技术,如外显子组测序,HLA分型,和RNA测序,这有助于鉴定TNBC特异性抗原和选择候选疫苗。然后讨论转移到计算机疫苗开发过程,包括抗原选择,表位预测,和合理的疫苗设计。此过程将计算模拟与免疫学见解合并。还强调了人工智能(AI)在加速抗原和表位预测中的作用。这篇综述总结了免疫信息学如何增强TNBC疫苗的设计,整合肿瘤抗原,先进的检测方法,计算机内战略,和AI驱动的见解,以推进TNBC免疫疗法。这可能为更有针对性和有效的治疗铺平道路。
    Triple-Negative Breast Cancer (TNBC) presents a significant challenge in oncology due to its aggressive behavior and limited therapeutic options. This review explores the potential of immunotherapy, particularly vaccine-based approaches, in addressing TNBC. It delves into the role of immunoinformatics in creating effective vaccines against TNBC. The review first underscores the distinct attributes of TNBC and the importance of tumor antigens in vaccine development. It then elaborates on antigen detection techniques such as exome sequencing, HLA typing, and RNA sequencing, which are instrumental in identifying TNBC-specific antigens and selecting vaccine candidates. The discussion then shifts to the in-silico vaccine development process, encompassing antigen selection, epitope prediction, and rational vaccine design. This process merges computational simulations with immunological insights. The role of Artificial Intelligence (AI) in expediting the prediction of antigens and epitopes is also emphasized. The review concludes by encapsulating how Immunoinformatics can augment the design of TNBC vaccines, integrating tumor antigens, advanced detection methods, in-silico strategies, and AI-driven insights to advance TNBC immunotherapy. This could potentially pave the way for more targeted and efficacious treatments.
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  • 文章类型: Journal Article
    目的:回顾组学技术在植物学研究领域的应用,并对新兴的机遇和挑战提供重要见解。
    方法:截至2022年12月,有关组学技术在Cariology研究中的应用的出版物均来自在线数据库,包括PubMed,WebofScience和Scopus两名独立审稿人评估了出版物与本审查目标的相关性。
    方法:采用组学技术调查龋齿的研究是从最初的已确定出版物中选择的。共有922种出版物采用了一种或多种组学技术,用于综合书目分析。(meta)基因组学(676/922,73%)是纳入研究中用于生态学研究的主要组学技术。其他应用的组学技术是代谢组学(108/922,12%),蛋白质组学(105/922,11%),和转录组学(76/922,8%)。
    结论:这项研究确定了在人类学研究中应用多种组学技术的新兴趋势。组学技术在开发检测策略方面具有巨大潜力,分期评估,风险评估,预防,和龋齿的管理。尽管前面有许多挑战,整合从单个生物样本中获得的多组数据,结合人工智能技术,可能为龋齿研究提供进一步探索的潜在途径。
    结论:这篇综述全面概述了组学技术在理学研究中的应用,并讨论了使用这些方法检测的优势和挑战,评估,预测,防止,治疗龋齿。它有助于指导研究,以提高对龋齿的理解并促进Cariology研究成果的临床翻译。
    To review the application of omics technologies in the field of cariology research and provide critical insights into the emerging opportunities and challenges.
    Publications on the application of omics technologies in cariology research up to December 2022 were sourced from online databases, including PubMed, Web of Science and Scopus. Two independent reviewers assessed the relevance of the publications to the objective of this review.
    Studies that employed omics technologies to investigate dental caries were selected from the initial pool of identified publications. A total of 922 publications with one or more omics technologies adopted were included for comprehensive bibliographic analysis. (Meta)genomics (676/922, 73 %) is the predominant omics technology applied for cariology research in the included studies. Other applied omics technologies are metabolomics (108/922, 12 %), proteomics (105/922, 11 %), and transcriptomics (76/922, 8 %).
    This study identified an emerging trend in the application of multiple omics technologies in cariology research. Omics technologies possess significant potential in developing strategies for the detection, staging evaluation, risk assessment, prevention, and management of dental caries. Despite the numerous challenges that lie ahead, the integration of multi-omics data obtained from individual biological samples, in conjunction with artificial intelligence technology, may offer potential avenues for further exploration in caries research.
    This review presented a comprehensive overview of the application of omics technologies in cariology research and discussed the advantages and challenges of using these methods to detect, assess, predict, prevent, and treat dental caries. It contributes to steering research for improved understanding of dental caries and advancing clinical translation of cariology research outcomes.
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  • 文章类型: Journal Article
    铜绿假单胞菌的生物膜形成是人类慢性伤口和肺部感染的主要原因。由于生物膜对抗菌药物的高耐受性和不断变化的环境因素,这些感染是持续存在的。了解控制生物膜形成的机制可以帮助开发明确针对负责该过程的分子标记的疗法。经过多年的研究,许多负责体外和体内生物膜发育的基因仍未被鉴定。然而,没有完整的体内或体外生物膜模型。最近的发现表明,从浮游细菌到生物膜的转变是一个复杂且相互关联的分化过程。组学技术在铜绿假单胞菌生物膜开发中的应用研究正在进行中,这些方法对扩大我们对生物膜形成机制的认识大有希望。这篇综述讨论了影响生物膜形成的不同因素,并使用针对基本生物大分子的组学方法比较了铜绿假单胞菌生物膜的形成。比如DNA,RNA,蛋白质,和代谢组。此外,我们已经概述了当前可用的组学工具的应用,比如基因组学,蛋白质组学,代谢组学,转录组学,和综合的多组学方法,了解差异基因表达(生物膜与浮游细菌)铜绿假单胞菌生物膜。
    Biofilm formation by Pseudomonas aeruginosa is primarily responsible for chronic wound and lung infections in humans. These infections are persistent owing to the biofilm\'s high tolerance to antimicrobials and constantly changing environmental factors. Understanding the mechanism governing biofilm formation can help to develop therapeutics explicitly directed against the molecular markers responsible for this process. After numerous years of research, many genes responsible for both in vitro and in vivo biofilm development remain unidentified. However, there is no \"all in one\" complete in vivo or in vitro biofilm model. Recent findings imply that the shift from planktonic bacteria to biofilms is a complicated and interrelated differentiation process. Research on the applications of omics technologies in P. aeruginosa biofilm development is ongoing, and these approaches hold great promise for expanding our knowledge of the mechanisms of biofilm formation. This review discusses the different factors that affect biofilm formation and compares P. aeruginosa biofilm formation using the omics approaches targeting essential biological macromolecules, such as DNA, RNA, Protein, and metabolome. Furthermore, we have outlined the application of currently available omics tools, such as genomics, proteomics, metabolomics, transcriptomics, and integrated multi-omics methodologies, to understand the differential gene expression (biofilm vs. planktonic bacteria) of P. aeruginosa biofilms.
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  • 文章类型: Review
    背景:术语“血管性认知障碍”(VCI)描述了包括血管成分的各种认知状况。它增加了老年人群的发病率和死亡率的风险,是与脑血管疾病相关的最常见的认知障碍。了解VCI的病因可能有助于确定针对该疾病的可能治疗方法。VCI的治疗集中在血管危险因素上。目前尚无授权的常规疗法。用于治疗VCI的药物仅被批准用于缓解症状,并不旨在预防或减缓VCI的发展。
    目的:中医药治疗VCI的作用尚未得到全面研究。这篇综述评估了临床前和有限的临床证据,以理解“多组分,多目标,多途径“中医机制”。它研究了寻找VCI病理机制的各种多组学方法,以及新的研究策略,希望为VCI的临床治疗提供支持性证据。
    方法:本综述将“首选报告项目”用于系统综述和荟萃分析(PRISMA)报表。使用集成的生物信息学和网络药理学方法,我们对截至2023年7月1日发表的25项临床前研究进行了全面评估和分析,以阐明中医治疗血管性认知障碍的机制.系统评价的研究使用以下数据库进行定位:PubMed,WebofScience,Scopus,科克伦,和科学直接。
    结果:我们发现,多组学分析方法将加速发现中医在VCI治疗中的作用。它将探索组件,化合物,目标,和路径,从抑制氧化应激的角度减缓VCI的进展,令人窒息的神经炎症,增加脑血流量,并通过多种分子机制抑制铁沉积,这对VCI的治疗有重要意义。
    结论:中医是发展痴呆疗法的宝贵工具,需要进一步的研究来确定中药成分如何影响神经血管单元的操作。还有一些局限性,尽管几项研究为寻找可能的抗痴呆药物和治疗提供了宝贵的资源。为了获得对分子机制的新见解,这些机制可以在药理干预期间精确调节不同水平的关键分子-理解作用机制和确定药物潜在治疗价值的先决条件-进一步的研究应采用更标准化的实验方法以及更复杂的科学技术。鉴于本次审查的结果,我们主张在未来的VCI研究中整合化学和生物成分分析方法,以更全面和客观地评估中药的标准。在生物信息学的帮助下,多组学分析方法将加速发现中医在VCI治疗中的作用,这对VCI的治疗具有重要意义.
    BACKGROUND: The term \"vascular cognitive impairment\" (VCI) describes various cognitive conditions that include vascular elements. It increases the risk of morbidity and mortality in the elderly population and is the most common cognitive impairment associated with cerebrovascular disease. Understanding the etiology of VCI may aid in identifying approaches to target its possible therapy for the condition. Treatment of VCI has focused on vascular risk factors. There are no authorized conventional therapies available right now. The medications used to treat VCI are solely approved for symptomatic relief and are not intended to prevent or slow the development of VCI.
    OBJECTIVE: The function of Chinese medicine in treating VCI has not yet been thoroughly examined. This review evaluates the preclinical and limited clinical evidence to comprehend the \"multi-component, multi-target, multi-pathway\" mechanism of Traditional Chinese medicine (TCM). It investigates the various multi-omics approaches in the search for the pathological mechanisms of VCI, as well as the new research strategies, in the hopes of supplying supportive evidence for the clinical treatment of VCI.
    METHODS: This review used the Preferred Reporting Items for Preferred reporting items for systematic reviews and meta-analyses (PRISMA) statements. Using integrated bioinformatics and network pharmacology approaches, a thorough evaluation and analysis of 25 preclinical studies published up to July 1, 2023, were conducted to shed light on the mechanisms of TCM for vascular cognitive impairment. The studies for the systematic review were located using the following databases: PubMed, Web of Science, Scopus, Cochrane, and ScienceDirect.
    RESULTS: We discovered that the multi-omics analysis approach would hasten the discovery of the role of TCM in the treatment of VCI. It will explore components, compounds, targets, and pathways, slowing the progression of VCI from the perspective of inhibiting oxidative stress, stifling neuroinflammation, increasing cerebral blood flow, and inhibiting iron deposition by a variety of molecular mechanisms, which have significant implications for the treatment of VCI.
    CONCLUSIONS: TCM is a valuable tool for developing dementia therapies, and further research is needed to determine how TCM components may affect the operation of the neurovascular unit. There are still some limitations, although several research have offered invaluable resources for searching for possible anti-dementia medicines and treatments. To gain new insights into the molecular mechanisms that precisely modulate the key molecules at different levels during pharmacological interventions-a prerequisite for comprehending the mechanism of action and determining the potential therapeutic value of the drugs-further research should employ more standardized experimental methods as well as more sophisticated science and technology. Given the results of this review, we advocate integrating chemical and biological component analysis approaches in future research on VCI to provide a more full and objective assessment of the standard of TCM. With the help of bioinformatics, a multi-omics analysis approach will hasten the discovery of the role of TCM in the treatment of VCI, which has significant implications for the treatment of VCI.
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