2023
DOI: 10.1016/j.ncrna.2023.02.001
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Exosomal non coding RNAs as a novel target for diabetes mellitus and its complications

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Cited by 23 publications
(18 citation statements)
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“…Recent studies have identified a variety of long non-coding RNAs (lncRNAs) in exosomes. 123 , 124 Li et al have indicated that mesenchymal stem cells-derived lncRNA H19 accelerates wound healing by enhancing PTEN via microRNA-152-3p in DFUs. 125 Yang et al also showed that HF-MSC-Exo markedly suppressed the production of IL-1β and IL-18 and activation of Caspase-1 and decreased the presence of the NLRP3 inflammasome in HaCaT cells.…”
Section: Suppressing Pyroptosis-dependent Signaling In Therapeutic Re...mentioning
confidence: 99%
“…Recent studies have identified a variety of long non-coding RNAs (lncRNAs) in exosomes. 123 , 124 Li et al have indicated that mesenchymal stem cells-derived lncRNA H19 accelerates wound healing by enhancing PTEN via microRNA-152-3p in DFUs. 125 Yang et al also showed that HF-MSC-Exo markedly suppressed the production of IL-1β and IL-18 and activation of Caspase-1 and decreased the presence of the NLRP3 inflammasome in HaCaT cells.…”
Section: Suppressing Pyroptosis-dependent Signaling In Therapeutic Re...mentioning
confidence: 99%
“…LncRNAs structures are heterogeneous, with or without poly A tails [ [1] , [2] , [3] , [4] ]. Compared with mRNA, the expression level of lncRNA is lower, and the conservation between species is poor, and its expression has obvious tissue or cell specificity, mainly localized in the nucleus, and a few localized in the cytoplasm [ 1 , 3 , 5 ].…”
Section: Lncrnas Overviewmentioning
confidence: 99%
“…Long non-coding RNAs (lncRNAs) was originally considered as a by-product of RNA polymerase II (Pol II) transcription, and was regarded as the "noise" of genome transcription because it cannot encode protein [ [1] , [2] , [3] , [4] , [5] ]. In recent years, with the help of high-throughput omics technology, more and more lncRNAs have been annotated.…”
Section: Introductionmentioning
confidence: 99%
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“…Ще один механізм, який може пояснювати корисність МСК у лікуванні ЦД, полягає в їхній здатності до інгібування апоптозу (програмованої клітинної смерті) інсулінових клітин в підшлунковій залозі, що може допомогти під-тримувати їх кількість та забезпечити стійкий функціональний ефект [16].…”
Section: результати та їх обговоренняunclassified