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  1. Article ; Online: Analysis of the lncRNA-Associated Competing Endogenous RNA (ceRNA) Network for Tendinopathy.

    Huang, Bing-Zhe / Jing-Jing, Yang / Dong, Xiao-Ming / Zhuan Zhong / Xiao-Ning Liu

    Genetics research

    2022  Volume 2022, Page(s) 9792913

    Abstract: Background: We aimed to construct the lncRNA-associated competing endogenous RNA (ceRNA) network and distinguish feature lncRNAs associated with tendinopathy.: Methods: We downloaded the gene profile of GSE26051 from the Gene Expression Omnibus (GEO), ...

    Abstract Background: We aimed to construct the lncRNA-associated competing endogenous RNA (ceRNA) network and distinguish feature lncRNAs associated with tendinopathy.
    Methods: We downloaded the gene profile of GSE26051 from the Gene Expression Omnibus (GEO), including 23 normal samples and 23 diseased tendons. Differentially expressed mRNAs (DEmRNAs) and differentially expressed lncRNAs (DElncRNAs) were identified, and functional and pathway enrichment analyses were performed. Protein-protein interaction (PPI) network was constructed and further analyzed by module mining. Moreover, a ceRNA regulatory network was constructed based on the identified lncRNA-mRNA coexpression relationship pairs and miRNA-mRNA regulation pairs.
    Results: We identified 1117 DEmRNAs and 57 DElncRNAs from the GEO data. The downregulated DEmRNAs were particularly associated with muscle contraction and muscle filament, while the upregulated ones were linked to extracellular matrix organization and cell adhesion. From the PPI network, 11 modules were extracted. Genes in MCODE 2 (such as TPM4) were significantly involved in cardiomyopathy, and genes in MCODE 4 (such as COL4A3 and COL4A4) were involved in focal adhesion, ECM-receptor interaction, and PI3K-Akt signaling pathway. The ceRNA network contained 7 lncRNAs (MIR133A1HG, LINC01405, PRKCQ-AS1, C10orf71-AS1, MBNL1-AS1, HOTAIRM1, and DNM3OS), 63 mRNAs, and 41 miRNAs. Downregulated lncRNA MIR133A1HG could competitively bind with hsa-miR-659-3p and hsa-miR-218-1-3p to regulate the TPM3. Meanwhile, MIR133A1HG could competitively bind with hsa-miR-1179 to regulate the COL4A3. Downregulated C10orf71-AS1 could competitively bind with hsa-miR-130a-5p to regulate the COL4A4.
    Conclusions: Seven important lncRNAs, particularly MIR133A1HG and C10orf71-AS1, were found associated with tendinopathy according to the lncRNA-associated ceRNA network.
    MeSH term(s) Gene Regulatory Networks/genetics ; Humans ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Phosphatidylinositol 3-Kinases/genetics ; RNA, Long Noncoding/genetics ; RNA, Long Noncoding/metabolism ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Tendinopathy/genetics
    Chemical Substances MIRN1179 microRNA, human ; MIRN218 microRNA, human ; MicroRNAs ; RNA, Long Noncoding ; RNA, Messenger
    Language English
    Publishing date 2022-05-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2412681-0
    ISSN 1469-5073 ; 0016-6723
    ISSN (online) 1469-5073
    ISSN 0016-6723
    DOI 10.1155/2022/9792913
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Leukocyte-Poor Platelet-Rich Plasma-Derived Growth Factors Enhance Human Fibroblast Proliferation

    Noh, Kyu-Cheol / Liu, Xiao Ning / Zhuan, Zhong / Yang, Cheol-Jung / Kim, Yong Tae / Lee, Geun Woo / Choi, Kyung Ho / Kim, Kyung-Ok

    Clinics in orthopedic surgery

    2018  Volume 10, Issue 2, Page(s) 240–247

    Abstract: Background: Leukocyte-poor platelet-rich plasma (LP-PRP) from peripheral blood is currently used as a concentrated source of growth factors to stimulate repair at sites of soft tissue injury. Fibroblasts are primary mediators of wound healing. Thus, we ... ...

    Abstract Background: Leukocyte-poor platelet-rich plasma (LP-PRP) from peripheral blood is currently used as a concentrated source of growth factors to stimulate repair at sites of soft tissue injury. Fibroblasts are primary mediators of wound healing. Thus, we aimed to assess the positive effect of LP-PRP on human fibroblast proliferation
    Methods: LP-PRP was prepared from 49 donors. The fibroblasts were seeded, and at 24 hours after seeding, 1 × 10
    Results: Human fibroblasts treated with LP-PRP showed a significant increase in proliferation when compared to untreated controls (
    Conclusions: Platelets in LP-PRP release growth factors such as PDGF, IGF-1, TGF-β1 and VEGF, and these growth factors have a promoting effect for human fibroblast proliferation, one of the important mediators of wound healing. These results suggest that growth factors derived from LP-PRP enhance the proliferation of human fibroblast.
    MeSH term(s) Cell Culture Techniques ; Cell Proliferation/drug effects ; Cells, Cultured ; Fibroblasts/cytology ; Fibroblasts/drug effects ; Humans ; Platelet-Derived Growth Factor/analysis ; Platelet-Derived Growth Factor/pharmacology ; Platelet-Rich Plasma/chemistry ; Platelet-Rich Plasma/cytology ; Transforming Growth Factor beta/analysis ; Transforming Growth Factor beta/pharmacology
    Chemical Substances Platelet-Derived Growth Factor ; Transforming Growth Factor beta
    Language English
    Publishing date 2018-05-18
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2502788-8
    ISSN 2005-4408 ; 2005-291X
    ISSN (online) 2005-4408
    ISSN 2005-291X
    DOI 10.4055/cios.2018.10.2.240
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Can a Single Sagittal Magnetic Resonance Imaging Slice Represent Whole Fatty Infiltration in Chronic Rotator Cuff Tears at the Supraspinatus?

    Lee, Yong-Beom / Yang, Cheol-Jung / Li, Cheng Zhen / Zhuan, Zhong / Kwon, Seung-Cheol / Noh, Kyu-Cheol

    Clinics in orthopedic surgery

    2018  Volume 10, Issue 1, Page(s) 55–63

    Abstract: Background: This study aimed to investigate whether fatty infiltration (FI) measured on a single sagittal magnetic resonance imaging (MRI) slice can represent FI of the whole supraspinatus muscle.: Methods: This study retrospectively reviewed the ... ...

    Abstract Background: This study aimed to investigate whether fatty infiltration (FI) measured on a single sagittal magnetic resonance imaging (MRI) slice can represent FI of the whole supraspinatus muscle.
    Methods: This study retrospectively reviewed the MRIs of 106 patients (age 50-79 years) divided into three rotator cuff tear-size groups: medium, large, and massive. Fat mass and muscle mass on all T1-weighted sagittal MRI scans (FA and MA) were measured. Of the total MRI scans, the Y-view was defined as the most lateral image of the junction of the scapular spine with the scapular body on the oblique sagittal T1-weighted image. Fat mass and muscle mass seen on this Y-view single slice were recorded as F1 and M1, respectively. Fat mass and muscle mass were also assessed on MRI scans lateral and medial to the Y-view. The means of fat mass and muscle mass on these three slices were recorded as F3 and M3, respectively. Average FI ratios (fat mass/muscle mass) of the three assessment methods (F1/M1, FA/MA, and F3/M3) were compared. Intraclass correlation coefficients (ICCs) were calculated for inter- and intraobserver reliability.
    Results: ICCs showed higher reliability (> 0.8) for all measurements. F1/M1 values were not statistically different from FA/MA and F3/M3 values (
    Conclusions: A single sagittal MRI slice can represent the whole FI in chronic rotator cuff tears, except in some patient groups. We recommend measurement of FI using a single sagittal MRI slice, given the effort required for repeated measurements.
    MeSH term(s) Adipose Tissue/diagnostic imaging ; Aged ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Observer Variation ; Reproducibility of Results ; Retrospective Studies ; Rotator Cuff Injuries/diagnostic imaging
    Language English
    Publishing date 2018-02-27
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2502788-8
    ISSN 2005-4408 ; 2005-291X
    ISSN (online) 2005-4408
    ISSN 2005-291X
    DOI 10.4055/cios.2018.10.1.55
    Database MEDical Literature Analysis and Retrieval System OnLINE

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