Publications by authors named "Jing-Yuan Xu"

Objectives: To systematically compare the effects of various antithrombotic strategies on prespecified outcomes including 28-day all-cause mortality (primary outcome), major thrombotic events and major bleeding events (secondary outcomes) in adult COVID-19 patients.

Design: Systematic review and Bayesian network meta-analysis (NMA).

Data Sources: PubMed, Web of Science, Embase, Cochrane Library and ClinicalTrials.

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Ovarian cancer (OC) is a lethal gynecologic malignancy with limited treatments. Platinum(II) drugs are commonly used but faced severe toxicities and resistance. This study developed theophylline-platinum(IV) prodrugs (-) to combat BRCA1-deficient OC via synthetic lethality strategy.

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Triple-negative breast cancer (TNBC) poses formidable challenges in the clinic owing to its particularly malignant and aggressive properties. Overexpression of eukaryotic elongation factor-2 kinase (eEF2K) is highly correlated with the poor prognosis of TNBC, representing a promising therapeutic target. Herein, Fluoxetine as eEF2K-inhibitor and chemosensitizer was conjugated with cisplatin/oxaliplatin to present two-in-one prodrugs -.

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Background: Recently, there has been an increasing interest in investigating the potential benefits or risks associated with using immunosuppressants for treating specific tumors post organ transplantation, with a focus on selecting appropriate drugs, doses, and treatment protocols. This study used bibliometric analysis to evaluate research trends and hotspots in this field.

Materials And Methods: A systematic search was conducted on the Web of Science to identify studies focusing immunosuppressants and cancer following organ transplantation from 2001 to 2023.

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Objectives: Sepsis-associated hypotension or shock is a critical stage of sepsis, and a current clinical emergency that has high mortality and multiple complications. A new restrictive fluid resuscitation therapy has been applied, and its influence on patients' renal function remains unclear. The purpose of this study is to evaluate the influence of restrictive fluid resuscitation on incidence of severe acute kidney injury (AKI) in adult patients with sepsis hypotension and shock compared with usual care.

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Convincing evidence revealed that some platinum-based drugs could stimulate immunological recognition, thereby inducing immunogenic cell death (ICD). Indoleamine-2,3-dioxygenase (IDO) is overexpressed in tumors, which caused exhaustion of tryptophan (T-cell energy) and constructed an immunosuppressive tumor microenvironment. Herein, considering IDO inhibition to improve chemotherapy, a series of IDOi-Pt(IV) prodrugs were designed to not only target DNA and IDO but also facilitate tumor-antigen exposure and immunomodulation.

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The examination of stamp impressions is a routine task for questioned document examiners (QDEs) in determining the authenticity of disputed documents. Some studies have provided methods for date determination of stamp impressions, but each single method has its own limitations, so date determination of stamp impressions remains a challenge in case work. This study reports on the real case of a forged contract, in which pre-inked stamp impressions were made on blank paper without the knowledge of the stamp owner.

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Platinum(II)-based antitumor drugs are widely used in clinics but limited by severe side effects and resistance. Multi-target Platinum(IV) complexes are emerging as ideal alternatives. Heme oxygenase-1 (HO-1) works as a rate-limiting step in heme degradation and is overexpressed in malignant tumors.

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As naturally essential biomacromolecule, HSA has become diagnostic indicators for various diseases and universal carriers for anticancer drug delivery, therefore, fluorescence detection and labeling for HSA possess significant application value in the biomedical field. In this paper, hydrazide Schiff base fluorescent probe NDQC was designed and synthesized, which self-assembled into nanoparticles in aqueous solution system and demonstrated excellent selectivity and sensitivity towards HSA. Through displacement assay and molecular docking simulation, the binding of NDQC with HSA in FA1 site was demonstrated, thereby no obvious fluorescence signal presented for homologous protein BSA due to their structural differences in binding site.

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Aim: To establish an animal model of form deprivation amblyopia based on a simulated cataract intraocular lens (IOLs).

Methods: Poly(dimethyl siloxane)-SiO thin films (PSF) with different degrees of opacity as IOL materials were prepared. The light transmission of the PSF-IOL was measured, and its biosafety was determined by cell counting kit (CCK)-8 assay using the HLEC-B3 cell line and ARPE-19 cell line.

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Article Synopsis
  • - Colorectal cancer exhibits over-expression of TMEM16A and COX-2, which creates an opportunity for targeted treatments.
  • - Two new platinum (Pt(iv)) drug conjugates, complexes 1 and 2, were developed to enhance the efficacy of existing drugs such as cisplatin and oxaliplatin, with complex 2 showing higher toxicity against cancer cells.
  • - Complex 2 demonstrated a significantly greater ability to kill colorectal cancer cells (22-fold increase) and showed better selectivity towards cancer cells compared to normal cells, working by triggering multiple biological pathways involved in cancer progression.
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  • Printer source prediction helps determine which printer made a certain document, but it's getting harder with new cartridge options.
  • A new technique was developed to identify the printer's maker, model, and cartridges by examining sample documents from several popular brands.
  • This method was very accurate, with over 90% success in guessing the correct printer details, even when different cartridges were used.
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  • * It identifies a specific type of activated neutrophil undergoing reverse transendothelial migration (rTEM) that plays a key role in spreading inflammation during sepsis, using advanced techniques like single-cell RNA sequencing.
  • * The research shows that inflamed endothelial cells release extracellular vesicles that enhance rTEM in neutrophils, suggesting these vesicles are vital in regulating lung injury linked to sepsis-associated ARDS.
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  • Platinum(II) cancer drugs face challenges like side effects and drug resistance, which limit their effectiveness.
  • Researchers developed a novel octahedral platinum(IV) prodrug that combines with upconversion nanoparticles (UCNPs) to enhance the delivery and impact of cisplatin while minimizing side effects.
  • The resulting UCNP/Pt(IV)-RGD nanoparticles show strong anti-cancer effects in lab and live studies, with properties allowing for targeted therapy and real-time imaging to monitor treatment.
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A novel technique is introduced to predict the printer model used to produce a given document. Samples containing only a few letters printed under varying conditions (i.e.

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A novel multi-functional fluorescence probe HMIC based on hydrazide Schiff base has been successfully synthesized and characterized. It can distinguish Al/Zn/Cd in ethanol, in which fluorescence emission with different colors (blue for Al, orange for Zn, and green for Cd) were presented. The limits of detection of HMIC towards three ions were calculated from the titration curve as 7.

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Background: Recent clinical trials have evaluated the efficacy of vonoprazan-amoxicillin (VA) dual therapy as the first-line treatment for Helicobacter pylori infection in different regions with inconsistent results reported. In this systematic review and meta-analysis, we aimed to evaluate the efficacy of VA dual therapy compared to the currently recommended therapy for eradicating H. pylori.

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Article Synopsis
  • Gut microbiota dysbiosis significantly contributes to non-alcoholic fatty liver disease (NAFLD), with the gut-liver axis being pivotal in this process.
  • The study investigated the impact of deleting the PPARδ gene on gut microbiota and NAFLD in mice on high-fat and normal diets, revealing that PPARδ deletion worsened liver inflammation and gut barrier health.
  • Results showed that PPARδ-/- mice had reduced beneficial bacteria and increased harmful bacteria, linking these changes to the severity of NAFLD and associated metabolic and inflammatory indicators.
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Cancer treatment requires the participation of multiple targets/pathways, and single approach is hard to effectively curb the proliferation and metastasis of carcinoma cells. In this work, we conjugated FDA-approved riluzole and platinum(II) drugs into a series of unreported riluzole-Pt(IV) compounds, which were designed to simultaneously target DNA, the solute carrier family 7 member 11 (SLC7A11, xCT), and the human ether a go-go related gene 1 (hERG1), to exert synergistic anticancer effect. Among them, c,c,t-[PtCl(NH)(OH)(glutarylriluzole)] (compound 2) displayed excellent antiproliferative activity with IC value of 300-times lower than that of cisplatin in HCT-116, and optimal selectivity index between carcinoma and human normal liver cells (LO2).

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Article Synopsis
  • - A series of gallium(III) complexes were created and characterized using X-ray crystallography and density functional theory, focusing mainly on their cytotoxic effects against various human cancer cell lines.
  • - One specific complex, CP-, showed significant effectiveness in killing colon cancer cells (HCT116) with comparatively lower toxicity than conventional drugs like cisplatin and oxaliplatin.
  • - The study revealed that CP- induces apoptosis in cancer cells by affecting DNA-related protein expression and also demonstrated potential for use in colon cancer diagnosis and treatment due to its desirable emissive properties.
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Exploring multi-targeting chemotherapeutants with advantages over single-targeting agents and drug combinations is of great significance in drug discovery. Herein, we employed phytogenic evodiamine (EVO) and conventional Pt(II) drugs to design and synthesize multi-target EVO-Pt(IV) anticancer prodrugs (-). Among them, compound exhibited a 118-fold enhancement in the IC value compared to cisplatin and low toxicity to normal cells.

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Background: Gallium (III) metal-organic complexes have been shown to have the ability to inhibit tumor growth, but the poor water solubility of many of the complexes precludes further application. The use of materials with high biocompatibility as drug delivery carriers for metal-organic complexes to enhance the bioavailability of the drug is a feasible approach.

Methods: Here, we modified the ligands of gallium 8-hydroxyquinolinate complex with good clinical anticancer activity by replacing the 8-hydroxyquinoline ligands with 5-bromo-8-hydroxyquinoline (HBrQ), and the resulting Ga(III) + HBrQ complex had poor water solubility.

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Pt(IV) anticancer compounds have been developed for several decades to overcome the drawbacks of their Pt(II) congeners, and the reduction of Pt(IV) to Pt(II) has been commonly regarded as a necessary step in the activation of Pt(IV) compounds prior to targeting DNA. However, blockage of glutathione (GSH) biosynthesis resulted in a slight effect on the cytotoxicity of oxoplatin in yeast Saccharomyces cerevisiae strains, urging us to reconsider the mechanism of actions for the "inert" Pt(IV) complexes. Using X-ray absorption near-edge spectroscopy (XANES), our data demonstrated that Pt(IV) complex oxoplatin could bind to DNA in a tetravalent state.

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Combination of immune- and chemo-therapy has become a new trend in cancer treatment. Food and Drug Administration (FDA)-approved immune-modulatory agent, thalidomide, can modulate the related proteins of upstream signaling pathway of programmed cell death-ligand 1 (PD-L1), including nuclear transcription factor κB (NF-κB), hypoxia inducible factor-1α (HIF-1α), epidermal growth factor receptor (EGFR), and signal transducer and activator of transcription 3 (STAT3), all acting as key antitumor target proteins. In this work, we conjugated thalidomide with oxidized cisplatin to construct multi-functional Pt(IV) prodrugs, named thaliplatins 4-6, to investigate the anti-tumor effect of immuno- and chemo-therapy.

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