DataSheet1_Cationic Metal–Organic Framework-Based Mixed-Matrix Membranes for Fast Sensing and Removal of Cr2O72− Within Water.DOCX

Considering that metal–organic framework (MOF)-polymer mixed-matrix membranes (MMMs) can overcome the drawbacks of intrinsic fragility and poor processability of pure-MOF membranes, we designed MOF-based MMMs for efficient removal and fast fluorescence sensing of heavily toxic ions within water systems simultaneously. In this work, a series of MOF-based MMMs are prepared by mixing a hydrolytically stable cationic [Eu7 (mtb)5(H2O)16]·NO3 8DMA·18H2O (denoted as Eu-mtb) MOF material into poly (vinylidene fluoride) with high loadings up to 70%. The free volume at the interface between the polymer and Eu-mtb particles, combined with the permanent porosity and uniform distribution of Eu-mtb particles, enables these MMMs to show fast enrichment of Cr2O72- from solutions and consequently have a full contact between the analyte and MOFs. The developed Eu-mtb MMM (70wt% loading) thus shows both efficient removal and exceptional fluorescence sensing of Cr2O72- in aqueous media. The overall adsorption capacity of the Eu-mtb MMM (70 wt% loading) for Cr2O72- reaches up to 33.34 mg/g, which is 3.4 times that of powder-form Eu-mtb. The detection limit of the Eu-mtb MMM (70 wt% loading) for Cr2O72- is around 5.73 nM, which is lower than that of the reported powder-form Eu-mtb. This work demonstrates that it is feasible to develop flexible luminescent MOF-based MMMs as a significant platform for efficient removal and sensitive sensing of pollutants from water systems simultaneously.</p

Metabolic Effects of the <i>pksCT</i> Gene on Monascus aurantiacus Li As3.4384 Using Gas Chromatography–Time-of-Flight Mass Spectrometry-Based Metabolomics

Monascus spp. have been used for the production of natural pigments and bioactive compounds in China for several centuries. Monascus can also produce the mycotoxin citrinin, restricting its use. Disruption of the <i>pksCT</i> gene in Monascus aurantiacus Li AS3.4384 reduces citrinin production capacity of this strain (Monascus PHDS26) by over 98%. However, it is unclear how other metabolites of M. aurantiacus Li AS3.4384 (the wild-type strain) are affected by the <i>pksCT</i> gene. Here, we used metabolomic analyses to compare red yeast rice (RYR) metabolite profiles of the wild-type strain and Monascus PHDS26 at different stages of solid-state fermentation. A total of 18 metabolites forming components within the glycolysis, acetyl-CoA, amino acid, and tricarboxylic acid (TCA) cycle metabolic processes were found to be altered between the wild-type strain and Monascus PHDS26 at different stages of solid-state fermentation. Thus, these findings provide important insights into the metabolic pathways affected by the <i>pksCT</i> gene in M. aurantiacus

Synthesis, Crystal Structures, and Biological Activity Evaluation of Novel Xanthine Derivatives Containing a Pyrethroid Moiety

On the basis of the structures of natural xanthines and pyrethroid insecticides, a series of novel xanthine derivatives Ia–Is containing pyrethroid motifs were synthesized and identified by means of melting points, 1H NMR, 13C NMR, and HRMS. The single crystals of compounds In and Iq were obtained, which further confirmed the structures and configurations of this type of compounds. The biological tests showed that some of them exhibited favorable insecticidal activities toward Mythimna separata Walker and Plutella xylostella L. and were superior to the natural methylxanthine compound caffeine and comparable with the insecticide tetramethrin (e.g., compound Im: LC50 = 0.6162 mg/L, against P. xylostella). Among others, Im, Ib, Ij, and Ik could serve as new insecticidal leading structures for further study. Moreover, some of the compounds showed favorable fungicidal activities against a broad spectrum of plant pathogenic fungi (e.g., compound Ie: EC50 = 6.0922 μg/mL, against Physalospora piricola; EC50 = 9.0637 μg/mL, against Rhizoctonia cerealis), which in turn would be an exciting new finding in xanthine chemistry; Ie, Ih, and Ii could be novel fungicidal leading compounds for further investigation. The structure–activity relationships of the compounds were also analyzed and discussed in detail. The research results presented in this paper provide a useful reference and guidance for the development of new natural product-based agrochemicals

DataSheet_1_The necroptosis related gene LGALS3 can be used as a biomarker for the adverse progression from chronic HBV infection to HCC.docx

The number of patients with hepatocellular carcinoma (HCC) caused by hepatitis B virus (HBV) infection remains large, despite the remarkable effectiveness of antiviral drugs and vaccines for HBV in preventing and treating HBV infection. Necroptosis is closely related to the occurrence of inflammation, clearance of viral infection, and tumor progression. Presently, little is known about the changes in necroptosis-related genes in the progression from chronic HBV infection (CHI) to HBV-related hepatic fibrosis (HBV-HF) and HBV-related hepatocellular carcinoma (HBV-HCC). In this study, Cox regression analysis was performed using GSE14520 chip data and a necroptosis-related genes survival prognosis score (NRGPS) was established for HBV-HCC patients. NRGPS was constructed using three model genes (G6PD, PINK1 and LGALS3), and verified by data sequencing in the TCGA database. The HBV-HCC cell model was established by transfection of pAAV/HBV1.2C2, constructed by homologous recombination, into HUH7 and HEPG2 cells. The expression levels of G6PD, PINK1, and LGALS3 were detected using RT-qPCR. We further analyzed the expression of the model genes in GSE83148, GSE84044, and GSE14520 and found that LGALS3 was consistently highly expressed in CHI, high fibrosis score and high NRGPS. In addition, immune microenvironment analysis showed that LGALS3 was not only associated with the infiltration of regulatory T cells in the immune microenvironment but also with expression of CCL20 and CCR6. The expression levels of model genes, FOXP3 and CCR6, were analyzed using RT-qPCR in peripheral blood mononuclear cells of 31 hepatitis B surface antibody positive patients, 30 CHI, 21 HBV-HF, and 20 HBV-HCC. In further cell-model experiments, we analyzed the expression of CCL20 by RT-qPCR and the changes in cell proliferation and migration by CCK8 and transwell assays, respectively, in HBV-HCC cell models after LGALS3 knockdown. The findings of this study suggest that LGALS3 could be a biomarker for adverse progression following chronic HBV infection and may also be involved in the regulation of the immune microenvironment, making it a potential therapeutic target.</p

Enhanced Surface-Enhanced Raman Scattering (SERS) Sensitivity by the Self-Assembly of Silver Nanoparticles (Ag NPs) Laminated on Polydimethylsiloxane (PDMS)

Herein, a transparent and reproducible substrate, fabricated using polydimethylsiloxane (PDMS) laminated with self-assembled Ag nanoparticles (Ag NPs), was employed as a universal surface-enhanced Raman scattering (SERS) substrate for the detection of targets with various matrices. The Ag NPs were assembled in a two-dimensional manner via a self-assembly technique. Due to the electrostatic interaction between the Ag NPs, the reproducibility of the assembly was ensured by the fixed density of the assembled Ag NPs at saturated assembly states. The assembled pattern and plasmon resonance of the Ag NPs were well preserved during the molding and curing of PDMS. As a result, the Ag NP laminated PDMS film exhibited a SERS effect to the adsorbed p-aminothiophenol comparable to that of the assembled Ag NPs on a glass slide. Extra SERS enhancement was achieved by construction of a Ag (PDMS)/molecule/Ag (glass) configuration due to the electromagnetic coupling between the Ag NPs. The Raman scattering of 4-mercaptobenzoic acid and benzotriazole modified on the surfaces of a smooth Au electrode and copper foil, respectively, was detected with the aid of the Ag NP-laminated PDMS film. Furthermore, malachite green dispersed in a KBr solid matrix was quantitatively determined with a detection limit of 0.5 μg/g. It is suggested that the SERS enhancement and consequential SERS detection sensitivity of the target molecules may be further maximized by adjusting the distance between the target molecules and the Ag NPs laminated on the PDMS film.</p

DataSheet_1_Development and validation of a necroptosis-related gene prognostic score to predict prognosis and efficiency of immunotherapy in gastric cancer.docx

Necroptosis is a novel type of regulated cell death that is intimately associated with a variety of tumors. However, how necroptosis affects the identification of gastric cancer (GC) remains unclear. Here we seek to find new potential necroptosis-related biomarkers to predict GC prognosis and immunotherapy effect. We used Cox analysis to obtain shared prognostic markers related to necroptosis from five datasets (TCGA and four GEO datasets). Then, a necroptosis-related gene prognostic score (NRGPS) system was constructed using LASSO Cox regression, NRGPS consisting of three necroptosis-related mRNAs (AXL, RAI14, and NOX4) was identified, 31 pairs of GC and adjacent normal tissues from the Second Hospital of Harbin Medical University were collected and Real-Time Quantitative PCR (RT-qPCR) was used to detect the relative expression levels of the three necroptosis-related mRNAs, and external validation was performed on four GEO datasets (GSE84437, GSE26901, GSE62254 and GSE15459). In this study, Overall survival (OS) in the high-NRGPS group was significantly lower than in the low-NRGPS group. Cox regression analyses showed that NRGPS was an independent prognostic variable. Tumor-mutation-burden (TMB), tumor microenvironment (TME), microsatellite instability (MSI), and Tumor Immune Dysfunction and Exclusion (TIDE) scoring were used as predictors of the immunotherapy response. A cancer-friendly immune microenvironment, a high TIDE score, a low TMB, and a low MSI were all characteristics of the high-NRGPS group, and they all consistently showed that the issues seen there are related to immune escape in GC. The combination of three candidate genes may be an effective method for diagnostic assessment of GC prognosis and immunotherapy efficacy.</p