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      Plasma miR-19b, miR-34a, and miR-146a expression in patients with type 2 diabetes mellitus and cataract: A pilot study

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          Abstract

          Cataract is among the most common ocular complications in diabetes mellitus (DM). While microRNA (miRNA) dysregulations in DM have been previously reported, consensus is still lacking concerning miRNA expression in cataract. Furthermore, the miRNA profile in diabetic cataract patients remains largely unexplored, and data on plasma expression levels are limited. Our study aimed to assess the plasma levels of three distinct miRNA species (hsa-miR-19b, hsa-miR-34a, and hsa-miR-146a) implicated in the development of cataract and/or DM. We investigated the circulating miRNA expression in DM patients diagnosed with cataract, compared to a non-DM cataract group. We employed qRT-PCR for relative quantification experiments and subsequently conducted a correlation analysis between miRNA expression levels and clinical characteristics. Our findings reveal that hsa-miR-34a and hsa-miR-146a are differentially expressed in the two cohorts. However, no significant correlation was observed between the clinical variables and miRNA levels. In summary, our results suggest a potential role for hsa-miR-34a and hsa-miR-146a in the biology of diabetic cataract.

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          Most cited references72

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          Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation

          MicroRNAs (miRNAs) are a class of non-coding RNAs that play important roles in regulating gene expression. The majority of miRNAs are transcribed from DNA sequences into primary miRNAs and processed into precursor miRNAs, and finally mature miRNAs. In most cases, miRNAs interact with the 3′ untranslated region (3′ UTR) of target mRNAs to induce mRNA degradation and translational repression. However, interaction of miRNAs with other regions, including the 5′ UTR, coding sequence, and gene promoters, have also been reported. Under certain conditions, miRNAs can also activate translation or regulate transcription. The interaction of miRNAs with their target genes is dynamic and dependent on many factors, such as subcellular location of miRNAs, the abundancy of miRNAs and target mRNAs, and the affinity of miRNA-mRNA interactions. miRNAs can be secreted into extracellular fluids and transported to target cells via vesicles, such as exosomes, or by binding to proteins, including Argonautes. Extracellular miRNAs function as chemical messengers to mediate cell-cell communication. In this review, we provide an update on canonical and non-canonical miRNA biogenesis pathways and various mechanisms underlying miRNA-mediated gene regulations. We also summarize the current knowledge of the dynamics of miRNA action and of the secretion, transfer, and uptake of extracellular miRNAs.
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            An overview of microRNAs: Biology, functions, therapeutics, and analysis methods

            MicroRNAs (miRNAs) are a class of small noncoding RNAs, which function in posttranscriptional regulation of gene expression. They are powerful regulators of various cellular activities including cell growth, differentiation, development, and apoptosis. They have been linked to many diseases, and currently miRNA-mediated clinical trial has shown promising results for treatment of cancer and viral infection. This review provides an overview and update on miRNAs biogenesis, regulation of miRNAs expression, their biological functions, and role of miRNAs in epigenetics and cell-cell communication. In addition, alteration of miRNAs following exercise, their association with diseases, and therapeutic potential will be explained. Finally, miRNA bioinformatics tools and conventional methods for miRNA detection and quantification will be discussed.
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              MicroRNA biogenesis pathways in cancer.

              MicroRNAs (miRNAs) are critical regulators of gene expression. Amplification and overexpression of individual 'oncomiRs' or genetic loss of tumour suppressor miRNAs are associated with human cancer and are sufficient to drive tumorigenesis in mouse models. Furthermore, global miRNA depletion caused by genetic and epigenetic alterations in components of the miRNA biogenesis machinery is oncogenic. This, together with the recent identification of novel miRNA regulatory factors and pathways, highlights the importance of miRNA dysregulation in cancer.
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                Author and article information

                Journal
                Biomol Biomed
                Biomol Biomed
                Biomolecules and Biomedicine
                Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
                2831-0896
                2831-090X
                1 June 2024
                1 June 2024
                : 24
                : 3
                : 537-544
                Affiliations
                [1 ]Doctoral School, “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania
                [2 ]Discipline of Ophthalmology, Department of Surgery I, “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania
                [3 ]Department of Ophthalmology, Municipal Emergency Clinical Hospital, Timisoara, Romania
                [4 ]Discipline of Biochemistry, Department of Biochemistry and Pharmacology, “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania
                [5 ]Center for Complex Network Science, “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania
                Author notes
                [* ]Correspondence to Mirabela Romanescu: mirabela.romanescu@ 123456umft.ro
                Author information
                https://orcid.org/0009-0004-4252-5873
                https://orcid.org/0000-0002-1288-2595
                https://orcid.org/0000-0002-7848-1786
                https://orcid.org/0000-0001-7184-388X
                https://orcid.org/0000-0001-7838-177X
                https://orcid.org/0009-0007-8664-4622
                Article
                BB-24-537
                10.17305/bb.2023.9933
                11088884
                38018996
                1834a90d-bd9a-4b8f-93ad-62452977ea07
                © 2023 Milcu et al.

                This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).

                History
                : 15 October 2023
                : 28 November 2023
                : 19 November 2023
                Categories
                Research Article

                cataract,diabetes mellitus (dm),diabetic retinopathy (dr),micrornas (mirnas),biomarker,qrt-pcr

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