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Tumor immune microenvironment lncRNAs

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dc.contributor.authorPark, Eun-Gyeong-
dc.contributor.authorPyo, Sung-Jin-
dc.contributor.authorCui, Youxi-
dc.contributor.authorYoon, Sang-Ho-
dc.contributor.authorNam, Jin-Wu-
dc.date.accessioned2022-07-06T10:39:23Z-
dc.date.available2022-07-06T10:39:23Z-
dc.date.created2022-03-07-
dc.date.issued2022-01-
dc.identifier.issn1467-5463-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/139813-
dc.description.abstractLong non-coding ribonucleic acids (RNAs) (lncRNAs) are key players in tumorigenesis and immune responses. The nature of their cell type-specific gene expression and other functional evidence support the idea that lncRNAs have distinct cellular functions in the tumor immune microenvironment (TIME). To date, the majority of lncRNA studies have heavily relied on bulk RNA-sequencing data in which various cell types contribute to an averaged signal, limiting the discovery of cell type-specific lncRNA functions. Single-cell RNA-sequencing (scRNA-seq) is a potential solution for tackling this limitation despite the lack of annotations for low abundance yet cell type-specific lncRNAs. Hence, updated annotations and further understanding of the cellular expression of lncRNAs will be necessary for characterizing cell type-specific functions of lncRNA genes in the TIME. In this review, we discuss lncRNAs that are specifically expressed in tumor and immune cells, summarize the regulatory functions of the lncRNAs at the cell type level and highlight how a scRNA-seq approach can help to study the cell type-specific functions of TIME lncRNAs. © The Author(s) 2021. Published by Oxford University Press.-
dc.language영어-
dc.language.isoen-
dc.publisherNLM (Medline)-
dc.titleTumor immune microenvironment lncRNAs-
dc.typeArticle-
dc.contributor.affiliatedAuthorNam, Jin-Wu-
dc.identifier.doi10.1093/bib/bbab504-
dc.identifier.scopusid2-s2.0-85123813445-
dc.identifier.wosid000763000800038-
dc.identifier.bibliographicCitationBriefings in bioinformatics, v.23, no.1, pp.1 - 25-
dc.relation.isPartOfBriefings in bioinformatics-
dc.citation.titleBriefings in bioinformatics-
dc.citation.volume23-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage25-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaMathematical & Computational Biology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryMathematical & Computational Biology-
dc.subject.keywordPlusgenetics-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusmetabolism-
dc.subject.keywordPlusneoplasm-
dc.subject.keywordPlusnucleotide sequence-
dc.subject.keywordPlussequence analysis-
dc.subject.keywordPlustumor microenvironment-
dc.subject.keywordAuthorbulk RNA-sequencing-
dc.subject.keywordAuthorcell type-specific expression-
dc.subject.keywordAuthorimmune cells-
dc.subject.keywordAuthorlong non-coding RNA-
dc.subject.keywordAuthorsingle-cell RNA-sequencing-
dc.subject.keywordAuthortumor immune microenvironment-
dc.identifier.urlhttps://academic.oup.com/bib/article/23/1/bbab504/6458113-
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