PENGARUH GOOD CORPORATE GOVERNANCE, LIKUIDITAS, DAN UKURAN PERUSAHAAN TERHADAP PROFITABILITAS PADA PERUSAHAAN BUMN YANG TERMASUK DALAM IICG DENGAN STRUKTUR MODAL SEBAGAI VARIABEL INTERVENING

Penelitian ini bertujuan untuk menguji pengaruh Good Corporate Governance, likuiditas, dan ukuran perusahaan terhadap profitabilitas, dimediasi oleh struktur modal. Metode penelitian yang digunakan adalah metode penelitian kuantitatif. Populasi dalam penelitian ini adalah perusahaan BUMN yang termasuk dalam IICG. Teknik pengambilan sampel adalah teknik purposive sampling dengan jumlah sampel sebanyak 13 perusahaan. Jenis data yang digunakan adalah data sekunder dan teknik analisis yang digunakan adalah Struktur Equation Model dengan alat uji software SmartPLS. Hasil dalam penelitian menunjukkan bahwa Good Corporate Governance, likuiditas dan ukuran perusahaan berpengaruh signifikan terhadap struktur modal. Hasil penelitian juga menunjukkan bahwa struktur modal memediasi secara penuh pengaruh Good Corporate Governance dan ukuran perusahaan terhadap profitabilitas, namun memediasi parsial pengaruh likuiditas terhadap profitabilitas

Preparation of RGO/TiO2/Ag Aerogel and Its Photodegradation Performance in Gas Phase Formaldehyde

To increase the utilization ratio and catalytic efficiency of the nano TiO2, The RGO/TiO2/(Ag) powders and RGO/TiO2/Ag aerogel photocatalyst were designed and prepared. The composition and microstructure of RGO/TiO2/(Ag) powders and RGO/TiO2/Ag aerogel were studied, in addition, the photocatalytic activity of RGO/TiO2/(Ag) powders and RGO/TiO2/Ag aerogel was researched by the photocatalytic degradation behavior of formaldehyde solution and formaldehyde gas respectively. The result indicate that TiO2 is uniformly loaded on the surface of RGO with a particle size of 10 nm to 20 nm. When the amount of graphene oxide added is 1 wt%, RGO/TiO2 powder has the highest degradation effect on formaldehyde solution, in addition, the introduction of Ag can greatly improve the photocatalytic effect of the sample. The results also show that the pore size of RGO/TiO2/Ag aerogel is between 7.6 nm and 12.1 nm, and the degradation rate of formaldehyde gas is 77.08% within 2 hours

β-catenin-mediated YAP signaling promotes human glioma growth

Abstract Background Hippo/YAP pathway is known to be important for development, growth and organogenesis, and dysregulation of this pathway leads to tumor progression.We and others find that YAP is up-regulated in human gliomas and associated with worse prognosis of patients. However, the role and mechanism of YAP in glioma progression is largely unknown. Methods The expression of YAP in glioma tissues was detected by quantitative polymerase chain reaction (qPCR) and immunoblotting. The effect of YAP on glioma progression was examined using cell growth assays and intracranial glioma model. The effect of YAP on β-catenin protein level, subcellular location and transcription activity was examined by immunoblotting, immunofluorescence and RT-PCR. Results Firstly, knockdown of YAP inhibited glioma cell proliferation in vitro and tumor growth in vivo. In addition, YAP modulated the protein level, subcellular location and transcription activity of β-catenin via regulating the activity of GSK3β. Lastly, β-catenin partially mediated the effect of YAP on glioma cell proliferation. Conclusion Our findings identify that YAP promotes human glioma growth through enhancing Wnt/β-catenin signaling. In addition, this study provides a new crosstalk mechanism between Hippo/YAP and Wnt/β-catenin pathways, which suggests a new strategy for human glioma treatment

Electrochemical Voltammogram Recording for Identifying Varieties of Ornamental Plants

An electrochemical voltammogram recording method for plant variety identification is proposed. Electrochemical voltammograms of Vistula, Andromeda, Danuta, Armandii 'Apple Blossom,' Proteus, Hagley Hybrid, Violet Elizabeth, Kiri Te Kanawa, Regina, and Veronica's Choice were recorded using leaf extracts with two solvents under buffer solutions. The voltametric data recorded under different conditions were derived as scatter plots, 2D density patterns, and hot maps for variety identification. In addition, the voltametric data were further used for genetic relationship studies. The dendrogram deduced from the voltammograms was used as evidence for relationship study. The dendrogram deduced from voltametric data suggested the Andromeda, Danuta, Proteus, Regina, and Hagley Hybrid were closely related, while Violet Elizabeth and Veronica's Choice were closely related. In addition, Vistula and Armandii 'Apple Blossom' could be considered outliers among the varieties

Transcriptome analysis of Clematis lanuginosa: Novel features of the molecular events occurring under heat-shock stress

The weak heat tolerance of Clematis ornamental varieties negatively affects their ornamental qualities in the summer. To elucidate heat resistance mechanisms, Clematis lanuginosa, which is an important original parent of the Clematis large-flowered group of ornamental varieties, was selected for use in this study. Here, six libraries, including three biological replicates each of control and heat-shock stress samples, were determined using RNA-sequencing technology. In total, 62,050 unigenes were obtained, and 6,439 unigenes exceeded 1 kb in length. A total of 42,377 unigenes were annotated using six databases. Between the two treatments, 2,165 differentially expressed genes were identified, with 1,565 being up-regulated and 600 down-regulated. In addition, 51 heat-shock protein-encoding genes were identified, among which the small heat-shock proteins accounted for 68.63%. In total, two heat-shock factors and 12 ribosomal proteins were significantly up-regulated under heat-stress conditions. The differential expressions of ethylene-responsive transcription factor, chalcone synthase, cysteine-rich receptor-like kinase and aspartic protease unigenes in guard cells were induced by heat-shock. The data obtained will assist the elucidation of the molecular events underlying heat-stress responses in C. lanuginosa

GRP78 determines glioblastoma sensitivity to UBA1 inhibition-induced UPR signaling and cell death

Abstract Glioblastoma multiforme (GBM) is an extremely aggressive brain tumor for which new therapeutic approaches are urgently required. Unfolded protein response (UPR) plays an important role in the progression of GBM and is a promising target for developing novel therapeutic interventions. We identified ubiquitin-activating enzyme 1 (UBA1) inhibitor TAK-243 that can strongly induce UPR in GBM cells. In this study, we evaluated the functional activity and mechanism of TAK-243 in preclinical models of GBM. TAK-243 significantly inhibited the survival, proliferation, and colony formation of GBM cell lines and primary GBM cells. It also revealed a significant anti-tumor effect on a GBM PDX animal model and prolonged the survival time of tumor-bearing mice. Notably, TAK-243 more effectively inhibited the survival and self-renewal ability of glioblastoma stem cells (GSCs) than GBM cells. Importantly, we found that the expression level of GRP78 is a key factor in determining the sensitivity of differentiated GBM cells or GSCs to TAK-243. Mechanistically, UBA1 inhibition disrupts global protein ubiquitination in GBM cells, thereby inducing ER stress and UPR. UPR activates the PERK/ATF4 and IRE1α/XBP signaling axes. These findings indicate that UBA1 inhibition could be an attractive strategy that may be potentially used in the treatment of patients with GBM, and GRP78 can be used as a molecular marker for personalized treatment by targeting UBA1

Additional file 1: Figure S1. of β-catenin-mediated YAP signaling promotes human glioma growth

Generation of YAP down-regulation U87 and U251 cells. (A) The infection efficiency of scramble and shYAP lentivirus in U251 and U87 cells. U87 and U251 glioma cells were infected with viral supernatant and the infection efficacy was evaluated by GFP positive cells 72 h later. Scale bar, 100 μm. PH: Phase contrast. (B) Representative immunoblots of protein extraction from shYAP infected U251 and U87 glioma cells (up panel)and YAP protein levels were quantified (bottom panel). *** P < 0.001. (PDF 358 kb