Single-Cell Transcriptomic Approaches for Decoding Non-Coding RNA Mechanisms in Colorectal Cancer.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mahnoor Naseer Gondal, Hafiz Muhammad Umer Farooqi
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引用次数: 0

Abstract

Non-coding RNAs (ncRNAs) play crucial roles in colorectal cancer (CRC) development and progression. Recent developments in single-cell transcriptome profiling methods have revealed surprising levels of expression variability among seemingly homogeneous cells, suggesting the existence of many more cell types than previously estimated. This review synthesizes recent advances in ncRNA research in CRC, emphasizing single-cell bioinformatics approaches for their analysis. We explore computational methods and tools used for ncRNA identification, characterization, and functional prediction in CRC, with a focus on single-cell RNA sequencing (scRNA-seq) data. The review highlights key bioinformatics strategies, including sequence-based and structure-based approaches, machine learning applications, and multi-omics data integration. We discuss how these computational techniques can be applied to analyze differential expression, perform functional enrichment, and construct regulatory networks involving ncRNAs in CRC. Additionally, we examine the role of bioinformatics in leveraging ncRNAs as diagnostic and prognostic biomarkers for CRC. We also discuss recent scRNA-seq studies revealing ncRNA heterogeneity in CRC. This review aims to provide a comprehensive overview of the current state of single-cell bioinformatics in ncRNA CRC research and outline future directions in this rapidly evolving field, emphasizing the integration of computational approaches with experimental validation to advance our understanding of ncRNA biology in CRC.

解码结直肠癌非编码RNA机制的单细胞转录组学方法。
非编码rna (ncRNAs)在结直肠癌(CRC)的发生和发展中起着至关重要的作用。单细胞转录组分析方法的最新进展揭示了在看似均匀的细胞中令人惊讶的表达变异性水平,这表明存在比以前估计的更多的细胞类型。本文综述了近年来CRC中ncRNA的研究进展,重点介绍了单细胞生物信息学方法对其进行分析。我们探索用于CRC中ncRNA鉴定、表征和功能预测的计算方法和工具,重点是单细胞RNA测序(scRNA-seq)数据。该综述强调了关键的生物信息学策略,包括基于序列和基于结构的方法、机器学习应用和多组学数据集成。我们讨论了如何将这些计算技术应用于分析CRC中ncrna的差异表达、执行功能富集和构建涉及ncrna的调控网络。此外,我们研究了生物信息学在利用ncrna作为结直肠癌诊断和预后生物标志物方面的作用。我们还讨论了最近揭示结直肠癌中ncRNA异质性的scRNA-seq研究。本文旨在全面概述单细胞生物信息学在ncRNA CRC研究中的现状,并概述这一快速发展领域的未来发展方向,强调将计算方法与实验验证相结合,以推进我们对CRC中ncRNA生物学的理解。
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
Non-Coding RNA
Non-Coding RNA Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍: Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.
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