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      Identification of human placenta-derived circular RNAs and autophagy related circRNA-miRNA-mRNA regulatory network in gestational diabetes mellitus

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          Abstract

          Gestational diabetes mellitus (GDM) is a metabolic and reproductive disease with serious risks and adverse health effects. However, the pathophysiological mechanism of GDM, especially the roles of circRNAs in its pathogenesis, is largely unknown. The objective of this study was to identify and investigate the roles of circRNAs in GDM. In the current study, placental circRNA expression profiles of normal controls and GDM patients were analyzed using high-throughput sequencing. Bioinformatics analysis identified a total of 4,955 circRNAs, of which 37 circRNAs were significantly deregulated in GDM placentas compared with NC placentas. GO and KEGG enrichment analyses demonstrated that metabolic process-associated terms and metabolic pathways that may be related to GDM were significantly enriched. The biological characteristics of placenta-derived circRNAs, such as their stability and RNase R resistance, were also validated Bioinformatics prediction. Moreover, we constructed the autophagy related circRNA-miRNA-mRNA regulatory network and further functional analysis revealed that the circCDH2–miR-33b-3p–ULK1 axis may be associated with autophagy in the placentas of GDM patients. Our study indicates that aberrant expression of circRNAs may play roles in autophagy in GDM placentas, providing new insights into GDM.

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          Most cited references47

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          Autophagy: renovation of cells and tissues.

          Autophagy is the major intracellular degradation system by which cytoplasmic materials are delivered to and degraded in the lysosome. However, the purpose of autophagy is not the simple elimination of materials, but instead, autophagy serves as a dynamic recycling system that produces new building blocks and energy for cellular renovation and homeostasis. Here we provide a multidisciplinary review of our current understanding of autophagy's role in metabolic adaptation, intracellular quality control, and renovation during development and differentiation. We also explore how recent mouse models in combination with advances in human genetics are providing key insights into how the impairment or activation of autophagy contributes to pathogenesis of diverse diseases, from neurodegenerative diseases such as Parkinson disease to inflammatory disorders such as Crohn disease. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Autophagy fights disease through cellular self-digestion.

            Autophagy, or cellular self-digestion, is a cellular pathway involved in protein and organelle degradation, with an astonishing number of connections to human disease and physiology. For example, autophagic dysfunction is associated with cancer, neurodegeneration, microbial infection and ageing. Paradoxically, although autophagy is primarily a protective process for the cell, it can also play a role in cell death. Understanding autophagy may ultimately allow scientists and clinicians to harness this process for the purpose of improving human health.
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              The metabolic syndrome

              The metabolic syndrome is a common metabolic disorder that results from the increasing prevalence of obesity. The disorder is defined in various ways, but in the near future a new definition(s) will be applicable worldwide. The pathophysiology seems to be largely attributable to insulin resistance with excessive flux of fatty acids implicated. A proinflammatory state probably contributes to the syndrome. The increased risk for type 2 diabetes and cardiovascular disease demands therapeutic attention for those at high risk. The fundamental approach is weight reduction and increased physical activity; however, drug treatment could be appropriate for diabetes and cardiovascular disease risk reduction.
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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                30 November 2022
                2022
                : 13
                : 1050906
                Affiliations
                [1] 1 Department of Obstetrics and Gynecology , Renmin Hospital of Wuhan University , Wuhan, China
                [2] 2 Department of Obstetrics and Gynecology , Xiaogan Central Hospital Affiliated to Wuhan University of Science and Technology , Xiaogan, China
                [3] 3 Reproductive Medical Center/Hubei Medical Clinical Research Center for Assisted Reproductive Technology and Embryonic Development , Renmin Hospital of Wuhan University , Wuhan, China
                Author notes

                Edited by: Guang Ji, Shanghai University of Traditional Chinese Medicine, China

                Reviewed by: Maoxiang Qian, Fudan University, China

                Yanqi Dang, Shanghai University of Traditional Chinese Medicine, China

                *Correspondence: Jing Yang, dryangjing@ 123456whu.edu.cn

                This article was submitted to RNA, a section of the journal Frontiers in Genetics

                Article
                1050906
                10.3389/fgene.2022.1050906
                9748685
                36531251
                172d2d30-c39f-4b53-97c5-b632965642f2
                Copyright © 2022 Bao, Zhang, Liu, Wu and Yang.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 September 2022
                : 10 November 2022
                Funding
                Funded by: National Key Research and Development Program of China , doi 10.13039/501100012166;
                Award ID: 2018YFC1002804
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: 81771618
                Categories
                Genetics
                Original Research

                Genetics
                circular rna (circrna),gestational diabetes mellitus (gdm),autophagy,placenta,ulk1
                Genetics
                circular rna (circrna), gestational diabetes mellitus (gdm), autophagy, placenta, ulk1

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