Wogonin Restrains the Malignant Progression of Lung Cancer Through Modulating MMP1 and PI3K/AKT Signaling Pathway.

BACKGROUND: Wogonin, a natural flavonoid compound, represses cancer cell growth and induces cancer cell apoptosis in diverse malignancies. However, the function of Wogonin in lung cancer cells and its regulatory mechanism deserve to be identified. METHODS: A549 and H460 cells were treated with Wogonin, and the cell growth, apoptosis, migration and invasion were measured by CCK-8 and EdU, flow cytometry and Transwell assays. The targeted genes of Wogonin and lung cancer were identified from the TCMSP and Genecards databases, respectively. The STRING database and Cytoscape software were used to establish a PPI network and screen hub genes. GO and KEGG analysis was conducted to explore the functions and signal pathways related to the hub genes. MMP1 expression in lung cancer was analyzed using the UALCAN databases, and GSEA was performed utilizing LinkedOmics. Gelatin zymography assay was used to detect MMP1 activity. MMP1 mRNA expression was detected by qRT-PCR. Besides, MMP1, p-AKT and c-Myc protein were detected by Western Blot assay. RESULTS: Wogonin could suppress the proliferation, migration and invasion of A549 and H460 cells and induce apoptosis. GO and KEGG enrichment analysis revealed the hub genes were mostly enriched in re-entry into the mitotic cell cycle and apoptosis. The expression of MMP1 was markedly upregulated in lung squamous cell carcinoma, lung adenocarcinoma tissues, and lung cancer cell lines. Wogonin could significantly inhibit MMP1 expression and activity, and overexpression of MMP1 significantly reversed the effect of Wogonin on the malignant phenotypes of A549 and H460 cells. Wogonin inhibited the expression of p-AKT and c-Myc protein by regulating MMP1. CONCLUSION: Wogonin can repress lung cancer cells' growth and metastatic potential and promote cell apoptosis via repressing MMP1 expression and modulating PI3K/AKT signaling pathway.

Thinning intensity but not replanting different species affects soil N2O and CH4 fluxes in Cunninghamia lanceolata plantation.

Thinning and replanting are effective forest management measures to improve the stand structure and species composition of artificial forests. However, the effects of thinning and replanting on soil N2O and CH4 fluxes and their associations with changes in soil environment factors have been poorly understood in plantation forests. A 36-month field experiment was conducted to elucidate the effects of thinning and replanting different species on soil N2O and CH4 fluxes and related environmental factors in Cunninghamia lanceolata plantation on shallow soil. The experiment consisted of five treatments, uncut control (CK), moderate thinning + replanting evergreen seedlings (MTE), moderate thinning + replanting deciduous seedlings (MTD), heavy thinning + replanting evergreen seedlings (HTE), heavy thinning + replanting deciduous seedlings (HTD). Compared with the control, moderate and heavy thinning increased cumulative N2O emissions by 12.4% and 21.4%, respectively, and reduced CH4 cumulative uptake by 35.4% and 38.8%, respectively. However, the effects on soil N2O and CH4 fluxes replanting deciduous or evergreen seedlings were insignificant. The results showed that thinning increased N2O emissions and decreased CH4 uptake due to the increased soil temperature, labile C and N concentrations. Soil temperature was the dominant factor, and mineral N was a contributing factor affecting N2O and CH4 fluxes. The study concludes that thinning increased the global warming potential with N2O contributing more than CH4 (113.5%: -13.5%). Our findings highlight that thinning increased N2O emissions and decreased CH4 uptake with the increasing intensity and the replanting had no different effects between deciduous and evergreen seedlings on the fluxes of N2O and CH4 during the early years following thinning.

Long noncoding RNA regulatory factor X3- antisense RNA 1 promotes non-small cell lung cancer via the microRNA-577/signal transducer and activator of transcription 3 axis.

Lung cancer is the most frequent malignancy, and non-small cell lung cancer (NSCLC) is its most common pathological type. Molecular targeted therapy has been testified to be effective in intervening in the occurrence and development of malignancies. This study investigates the effect of lncRNA Regulatory Factor X3- antisense RNA 1 (RFX3-AS1) in NSCLC progression. The RFX3-AS1 profile in NSCLC tissues and cells was measured by quantitative reverse transcription PCR (qRT-PCR). The RFX3-AS1 overexpression model was constructed. The cell counting kit-8 (CCK-8) experiment and cell colony formation assay were adopted to test cell viability. The cell apoptosis was determined by flow cytometry (FCM). Cell migration and invasion were monitored by the Transwell assay, and Western blot was implemented to verify the protein profiles of signal transducer and activator of transcription 3 (STAT3), E-cadherin, Vimentin and N-cadherin. In vivo, we validated the impact of RFX3-AS1 overexpression on the NSCLC xenograft mouse model. The targeting relationships between RFX3-AS1 and miR-577, miR-577 and STAT3 were confirmed by the dual-luciferase reporter assay. The results manifested that overexpressing RFX3-AS1 markedly facilitated NSCLC cell proliferation, migration, invasion and epithelial-mesenchymal transition (EMT), and suppressed cell apoptosis. In contrast, miR-577, which was a downstream target of RFX3-AS1, dramatically impeded the malignant biological behaviors of NSCLC cells. STAT3 was a direct target of miR-577, and it was negatively regulated by the latter. STAT3 activation reversed miR-577-mediated anti-tumor roles. In brief, RFX3-AS1 aggravated NSCLC progression by regulating the miR-577/STAT3 axis.

Ion-Exchange Fabrication of Hierarchical Al-MOF-Based Resin Catalysts for the Tandem Reaction.

Metal-organic framework (MOF)-supported macroscale resin catalysts, IRA900(xOH)-MIL-101(Al)-NH2 (x means the concentration of NaOH), with spatially isolated antagonistic acid-base active sites were successfully synthesized through a novel strategy by ion exchange and in situ solvothermal methods. The hierarchical pore system of the as-prepared catalysts effectively promotes the mass transfer and contacts with catalytic active centers during the organic reactions. Therefore, the environmentally friendly catalysts exhibit excellent superior activity and stability in one-pot deacetalization-Knoevenagel condensation reaction, and the yield by optimal IRA900(0.2OH)-MIL-101(Al)-NH2 reaches close to 99% after 5 h at 110 °C. Thanks to the millimeter-sized resin carrier and robust sphere morphology, the recycling of the as-prepared catalysts only requires natural sedimentation. This work presents an effective strategy to build low-toxic acid-base catalysts by combining the advantages of ion-exchange resins and functionalized MOF materials.

A subanesthetic dose of sevoflurane combined with oxygen exerts bactericidal effects and prevents lung injury through the nitric oxide pathway during sepsis.

Volatile anesthetics have been proven to treat experimental sepsis. Sevoflurane combined with oxygen is widely applied in the clinic, and our previous study indicated that this regimen significantly reduced sepsis-induced inflammatory responses and that inhibition of NF-κB pathway activation may contribute to this protection effect. Furthermore, our previous data has shown that sevoflurane combined with oxygen has prevention effect on sepsis-induced lung injury properties and bactericidal properties, but the mechanism is not well understood. Nitric oxide (NO) has been shown to have bactericidal effects and mitigating effects on lung injury, but this is not well studied in sepsis. The present study suggested that in cecal ligation and puncture (CLP)-induced sepsis, sevoflurane combined with oxygen had bactericidal effects and reduced neutrophil infiltration into the lung, preventing inflammatory lung injury. NO production was significantly induced in peritoneal lavage fluid and bronchoalveolar lavage fluid. These effects were abolished by pharmacological inhibition of nitric oxide synthase activity. Thus, our findings suggest that sevoflurane combined with oxygen exerts bactericidal effects and prevents lung injury in sepsis through the NO pathway.

New Insights into Co-pyrolysis among Graphitic Carbon Nitride and Organic Compounds: Carbonaceous Gas Fragments Induced Synthesis of Ultrathin Mesoporous Nitrogen-Doped Carbon Nanosheets for Heterogeneous Catalysis.

N-doped carbon materials are well known as promising metal-free catalysts and applied in innumerable industrial synthetics. However, most of the N-doped carbon materials obtained by conventional synthetic means exhibit generally low mesoporosity, and their reported pore volumes reached only 1-3 cm3 g-1, which greatly limits their further industrial application in heterogeneous catalysis. Especially for oxidation reaction of alkylbenzenes, this type of reaction is almost always accompanied by many different byproducts, while the reaction activity and selectivity are mainly affected by mesoporosity of catalysts. Traditionally, graphitic carbon nitride (GCN) is commonly considered as a self-sacrificed nitrogen source together with multifarious organic compounds to obtain N-doped carbon materials by a co-pyrolysis process. However, the mechanisms of formation process are still complex and uncontrollable to date. In this work, we present a novel co-pyrolysis synthetic strategy by a facile chemical vapor deposition method for preparing a series of ultrathin N-doped carbon nanosheets with high mesoporosity. More importantly, it is found that GCN containing abundant hydrogen bonds can be irreversibly anchored by carbonaceous gas fragments (CxHy+) released from various organic substances via thermogravimetry-differential thermal analysis coupled with mass spectrometry and X-ray photoelectron spectroscopy analysis, and the CxHy+ fragments exhibit a non-negligible role during the transformation. Our results further demonstrated that the residue of incompletely decomposed GCN is a key point to enlarge porosity in final products which are obtained via mixing pyrolysis between an organic precursor and GCN (or GCN precursors). Benefitting from the outstanding mesoporosity and ultrathin morphology, the representative ABCNS-900 exhibits excellent catalytic performance for oxidizing ethylbenzene to acetophenone with extremely low dosage and high selectivity. Our findings show a universal synthetic strategy for ultrathin N-rich carbon nanosheets with a high mesopore volume, further promoting the application of N-doped carbon materials in heterogeneous catalytic industry.