2022
DOI: 10.1016/j.heliyon.2022.e09178
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The axis of long non-coding RNA MALAT1/miR-1-3p/CXCR4 is dysregulated in patients with diabetic neuropathy

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Cited by 19 publications
(13 citation statements)
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“…Long coding RNAs (lncRNA) such as MALAT1 and NEAT1 are known to interact with miRNAs and have been implicated in the pathogenesis of DN. 4,5,18 For example, MALAT1 acts as a sponge and binds to miR-1-3p and prevents its interaction with its target. This implies that upregulation of incRNAs may result in downregulation of miRNA as demonstrated in a few studies included in this review.…”
Section: Summary Of Findingsmentioning
confidence: 99%
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“…Long coding RNAs (lncRNA) such as MALAT1 and NEAT1 are known to interact with miRNAs and have been implicated in the pathogenesis of DN. 4,5,18 For example, MALAT1 acts as a sponge and binds to miR-1-3p and prevents its interaction with its target. This implies that upregulation of incRNAs may result in downregulation of miRNA as demonstrated in a few studies included in this review.…”
Section: Summary Of Findingsmentioning
confidence: 99%
“…4,5,38 In 4 of 7 studies (57%), DN and DPN were the population of interest. 4,5,27,38 The other 3 studies 16,25,29 included patients with neuropathic pain of various aetiology including diabetes and vascular and inflammatory neuropathies. Although miRNA expression in blood samples were used in 6 of 7 studies, nerve biopsy was used in one study.…”
Section: Description Of the Studies Includedmentioning
confidence: 99%
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“…LncRNA MALAT1 was significantly upregulated in the peripheral-blood mononuclear cells of patients with diabetic neuropathy [ 77 ]. Further, a significant positive association between MALAT1 and C-X-C motif chemokine receptor 4 (CXCR4) was observed.…”
Section: Dysregulated Human Ncrnas In Diabetesmentioning
confidence: 99%
“… 54 A similar result was observed for lncRNA‐GM4419 in renal tissue from T2D nephropathy mice and HG‐induced mesangial cells. 33 In addition, MALAT1 34 , 35 and SNHG5 36 were shown to regulate inflammation by targeting NLRP3 in T2D brain tissue or neuron cells, and SNHG2 55 , 56 was reported to modulate inflammation by regulating NF‐κB, while H19 37 and lnc uc.48 38 regulate inflammation by activating endoplasmic reticulum stress proteins (XBP1 or ERK), indicating that inflammatory responses are differentially regulated by lncRNAs. In addition, some lncRNAs regulate inflammation by epigenetic modification of inflammation‐related genes.…”
Section: Roles Of Lncrnas In Diabetesmentioning
confidence: 99%