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Gene & Protein in Disease                                 lncRNAs dysregulation in diabetes and its complications














































            Figure  2.  Role of long noncoding RNAs (lncRNAs) in kidney disease among diabetic patients. Dysregulation of upregulated lncRNAs—MALAT1,
            plasmacytoma variant translocation 1 (LncPVT1), and antisense noncoding mitochondrial RNA-2 (ASncmtRNA-2) and downregulated lncRNAs—
            CASC2, MIAT, and taurine-upregulated gene 1 (TUG1) is crucial in regulating inflammation within the extracellular matrix.
            Abbreviations: Blnc1: Brown fat lncRNA 1; CASC2: Cancer susceptibility candidate 2; CDKN2BAS1: Cyclin-dependent kinase inhibitor 2B antisense
            RNA 1; DIP5-AS1: Antisense RNA; Dlxos1: Distal-less homeobox 1 opposite strand; GAS5: Growth arrest-specific 5; GM5524: Noncoding RNA (mouse);
            GM15645: Non-coding RNA (mouse); GM4419: Noncoding RNA (mouse); H19: Imprinted maternally expressed transcript; HOXA-AS2: HOXA cluster
            antisense RNA 2; KCNN4: Potassium calcium-activated channel subfamily N member 4; KCNN1OT1: Potassium calcium-activated channel subfamily
            N member 1 overlapping transcript 1; lncRNA 9884: Long noncoding RNA 9884; lncRNA 00462: Long noncoding RNA 00462; Long noncoding RNA;
            MALAT1: Metastasis associated lung adenocarcinoma transcript 1; MEG3: Maternally expressed gene 3; MIAT: Myocardial infarction associated
            transcript; PVT1: Plasmacytoma variant translocation 1; NEAT1: Nuclear enriched abundant transcript 1; RPPH1: Ribonuclease P RNA component H1;
            SOX2OT: SOX2 overlapping transcript; SHNG16: Specific RNA sequence; SPAG5-AS1: Sperm associated antigen 5 antisense RNA 1; UCA1: Urothelial
            cancer-associated 1; ZEB1-AS1: Zinc finger E-box binding homeobox 1 antisense RNA 1; 4930551F19Rik: Noncoding RNA (mouse).

              Similarly, other lncRNAs, such as testis development-  is characterized by cardiac dysfunction in patients without
            related gene 1, are dysregulated in DR, promoting   coronary artery disease, hypertension, or valvular heart
            microvascular complications. In contrast, lncRNAs like   disease. 65,66  Several pathogenic factors contribute to DCM,
            x-inactive specific transcript and lung adenocarcinoma-  including oxidative stress, mitochondrial dysfunction,
            associated transcript 1 are downregulated, inducing retinal   inflammation, impaired calcium handling, angiotensin-
            cell apoptosis (Table 3). These findings indicate that the   converting enzyme activation, and cardiomyocyte
            dysregulation of specific lncRNAs plays a key role in DR   apoptosis.  The lncRNA H19 plays a key role in DCM,
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            pathogenesis, suggesting potential therapeutic targets.  producing a 2.6 kb ncRNA that is polyadenylated, spliced,
                                                               and mainly localized in the cytoplasm, with some presence
            4.3. LncRNAs and diabetic cardiomyopathy (DCM)     in the nucleus. Acute hyperinsulinemia downregulates
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            DCM, significant cardiac complications of DM, is marked   H19.  H19 interacts with the DIRAS3 promoter, recruiting
            by a high risk of heart failure and increased mortality.  It   the histone methyltransferase EZH2 to mediate epigenetic
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            Volume 4 Issue 2 (2025)                         6                               doi: 10.36922/gpd.4000
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