2022
DOI: 10.1007/s11033-022-08080-y
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lncRNAs dysregulation in monocytes from primary antiphospholipid syndrome patients: a bioinformatic and an experimental proof-of-concept approach

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Cited by 8 publications
(9 citation statements)
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“…Interestingly, a recent experimental study characterizing the molecular signature of 54 biopsy specimens from lupus nephritis patients demonstrated that the aforementioned lncRNA TP53TG1 inversely correlated with the degree of glomerulosclerosis [55]. Conversely, none of the lncRNAs reported in studies of APS patients correlated with lncRNAs that showed alignment with syncytin-1 or syncytin-2 genes [32,33]. Table 5.…”
Section: Discussionmentioning
confidence: 99%
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“…Interestingly, a recent experimental study characterizing the molecular signature of 54 biopsy specimens from lupus nephritis patients demonstrated that the aforementioned lncRNA TP53TG1 inversely correlated with the degree of glomerulosclerosis [55]. Conversely, none of the lncRNAs reported in studies of APS patients correlated with lncRNAs that showed alignment with syncytin-1 or syncytin-2 genes [32,33]. Table 5.…”
Section: Discussionmentioning
confidence: 99%
“…Unfortunately, there are no studies investigating the occurrence of dysregulated synthesis of the HERV-derived env proteins syncytin-1 and syncytin-2 in SLE patients. The role of syncytins in APS pathogenesis also remains unknown, although some recent studies have reported an altered lncRNA signature in these patients compared with controls [32,33]. Indeed, lncRNAs may contribute to several steps of APS pathogenesis, including leukocyte activation, immunothrombosis, and impaired embryonic development [34], but whether these events are influenced by the abnormal expression of syncytin genes has not been investigated to date.…”
Section: Discussionmentioning
confidence: 99%
“…In this line of information, lncRNA HOTAIRM1 has been described to play a critical role in inflammatory and allergic response; one study led by Lihua Li and collaborators found that HOTAIRM1 are implicated in allergic rhinitis by promoting differentiation of T helper type 9 cells through miR-148a-3p interaction [ 23 ]. Similarly, in recent years, MZF1-AS1 has been proposed as a promising actor in different pathological phenotypes, including autoimmunity, cancer, and chronic pulmonary diseases [ 18 , 24 , 25 ]. In sum, these studies suggest that overexpression of OIP5-AS1, GAS5, HOTAIRM1, and MZF1-AS1 play crucial roles in the pathophysiology of several diseases in which more severe states are related; and as we can observe in the bioinformatic interaction pathways image, OIP5-AS1, MZF1-AS1, HOTAIRM1, and GAS5 may indirectly interact with genes and microRNAs that have been described as critical components of the role of low-grade inflammation (i.e., meta inflammation) in some endotypes of asthma, which make us hypothesize that whole blood overexpression of these lncRNAs may be part of a characteristic phenotype of asthmatic patients.…”
Section: Discussionmentioning
confidence: 99%
“…In recent years, emerging evidence has shed light on the involvement of lncRNAs in keratinocyte biology [ 14 , 15 ]. LncRNAs are transcripts that do not code for proteins of >200 pb in length, once considered transcriptional "noise," are now recognized as key players in gene regulation and have garnered attention for their potential implication in diverse cellular processes [ 16 , 17 ]. Dysregulation of specific lncRNAs can disrupt this balance, leading to abnormal keratinocyte proliferation, impaired differentiation, and compromised barrier integrity, contributing to the pathogenesis of skin disorders such as psoriasis, atopic dermatitis, and skin cancers [ 18 ].…”
Section: Introductionmentioning
confidence: 99%