CuFe2O4/lignin-based carbon composited photothermal and photodynamic agents for synergetic antibacterial therapy.

Bacterial infection has become the second leading cause of death in the world. Exploring a new highly antibacterial catalyst to replace traditional antibacterial agent is crucial for the society development of human beings. In this study, CuFe2O4/Lg-based carbon composited catalysts were rationally constructed by facile hydrothermal method. Lignin-derived carbon with enormous oxygen-containing functional group was beneficial to anchor CuFe2O4 nanoparticles. The close contact interface between CuFe2O4 and Lignin-based carbon material was expected to extend the range of optical absorption and promote the separation and transportation of photogenerated carriers. Under NIR (980 nm, 1.5 W/cm2) light irradiation, the as-prepared CuFe2O4/Lg (20 µg/mL) exhibited excellent photo/photothermal synergetic in vitro (against Escherichia coli and Staphylococcus aureus) and in vivo (against Staphylococcus aureus-infected mouse wound model) antibacterial performance. Furthermore, the cell count assay kit 8 (CCK-8 kit) demonstrated the good biocompatibility of this material. On the basis of the experimental results, a possible antibacterial mechanism based on the synergetic photothermal and photodynamic therapies was proposed. This work presented a lignin- derived carbon-based highly efficient antibacterial disinfection agent with desirable biosafety.

Metabolic subtypes and immune landscapes in esophageal squamous cell carcinoma: prognostic implications and potential for personalized therapies.

BACKGROUND: This study aimed to identify metabolic subtypes in ESCA, explore their relationship with immune landscapes, and establish a metabolic index for accurate prognosis assessment. METHODS: Clinical, SNP, and RNA-seq data were collected from 80 ESCA patients from the TCGA database and RNA-seq data from the GSE19417 dataset. Metabolic genes associated with overall survival (OS) and progression-free survival (PFS) were selected, and k-means clustering was performed. Immune-related pathways, immune infiltration, and response to immunotherapy were predicted using bioinformatic algorithms. Weighted gene co-expression network analysis (WGCNA) was conducted to identify metabolic genes associated with co-expression modules. Lastly, cell culture and functional analysis were performed using patient tissue samples and ESCA cell lines to verify the identified genes and their roles. RESULTS: Molecular subtypes were identified based on the expression profiles of metabolic genes, and univariate survival analysis revealed 163 metabolic genes associated with ESCA prognosis. Consensus clustering analysis classified ESCA samples into three distinct subtypes, with MC1 showing the poorest prognosis and MC3 having the best prognosis. The subtypes also exhibited significant differences in immune cell infiltration, with MC3 showing the highest scores. Additionally, the MC3 subtype demonstrated the poorest response to immunotherapy, while the MC1 subtype was the most sensitive. WGCNA analysis identified gene modules associated with the metabolic index, with SLC5A1, NT5DC4, and MTHFD2 emerging as prognostic markers. Gene and protein expression analysis validated the upregulation of MTHFD2 in ESCA. MTHFD2 promotes the progression of ESCA and may be a potential therapeutic target for ESCA. CONCLUSION: The established metabolic index and identified metabolic genes offer potential for prognostic assessment and personalized therapeutic interventions for ESCA, underscoring the importance of targeting metabolism-immune interactions in ESCA. MTHFD2 promotes the progression of ESCA and may be a potential therapeutic target for ESCA.

Single-cell multi-omics in the study of digestive system cancers.

Digestive system cancers are prevalent diseases with a high mortality rate, posing a significant threat to public health and economic burden. The diagnosis and treatment of digestive system cancer confront conventional cancer problems, such as tumor heterogeneity and drug resistance. Single-cell sequencing (SCS) emerged at times required and has developed from single-cell RNA-seq (scRNA-seq) to the single-cell multi-omics era represented by single-cell spatial transcriptomics (ST). This article comprehensively reviews the advances of single-cell omics technology in the study of digestive system tumors. While analyzing and summarizing the research cases, vital details on the sequencing platform, sample information, sampling method, and key findings are provided. Meanwhile, we summarize the commonly used SCS platforms and their features, as well as the advantages of multi-omics technologies in combination. Finally, the development trends and prospects of the application of single-cell multi-omics technology in digestive system cancer research are prospected.

Dynamic Adsorption Properties of Insoluble Humic Acid/Tourmaline Composite Particles for Iron and Manganese in Mine Wastewater.

Iron- and manganese-contaminated mine water is widespread around the world, and economical and efficient remediation has become a priority. Insoluble humic acid/tourmaline composite particles (IHA/TM) were prepared by combining inorganic tourmaline (TM) with the natural organic polymer humic acid (HA), and the effects of different calcination temperatures and calcination times of TM and IHA on the adsorption of Fe2+ and Mn2+ were analyzed. Based on the microscopic characterization of Scanning electron microscopy (SEM), Energy Dispersive Spectroscopy (EDS), Brunnauer-Emmet-Teller (BET), X-ray diffractometer (XRD) and Fourier transform infrared (FTIR), the simultaneous adsorption performance of IHA/TM on Fe2+ and Mn2+ was studied through dynamic adsorption tests, and a dynamic adsorption model was established. Adsorption regeneration experiments were carried out to further investigate the effectiveness of the composite particles in practical applications. The results show that, when the calcination temperature was 330 °C and the calcination time was 90 min, the removal rates of iron and manganese by the IHA/TM composite particles reached 99.85% and 99.51%, respectively. The curves for penetration of Fe2+ and Mn2+ ions into the IHA/TM composite particles were affected by the bed height, flow rate and influent concentration. Decreasing the flow rate, decreasing the influent concentration, or increasing the bed height prolonged the operation time of the dynamic column. If the bed height was too low, the penetration point was reached before the expected treatment was achieved, and when the bed height was too high, the removal of Fe2+ and Mn2+ was slow, and the utilization rate of the adsorbent was also reduced. If the flow rate was too low, longitudinal remixing easily occurred in the column. However, when the flow rate was too high, the speed of Fe2+ and Mn2+ ions passing through the adsorption layer increased, which reduced the total amount of adsorption. The increase in influent concentration not only reduces the removal rate, but also greatly shortens the total operation time of the dynamic column and reduces the treatment water. The dynamic process for the adsorption of Fe2+ and Mn2+ by IHA/TM was fitted best by the Thomas model. The adsorption column was continuously regenerated five times, and the results show that the IHA/TM composite particles were suitable for iron and manganese removal from mine wastewater. The research results will provide a reference for the effectiveness of the IHA/TM composite particles in practical applications.

Removal of Fe2+ and Mn2+ from Polluted Groundwater by Insoluble Humic Acid/Tourmaline Composite Particles.

Insoluble humic acid/tourmaline composite particles (IHA/TM) were prepared by combining inorganic tourmaline (TM) with the natural organic polymer humic acid (HA) and carbonizing them at 330 °C to study the removal characteristics and mechanism of Fe2+ and Mn2+. The results showed that the optimal ratio of TM to IHA is 2:3. When the temperature of the IHA/TM composite particles was 35 °C and the pH was 6, the adsorption of Fe2+ and Mn2+ by IHA/TM reached equilibrium at 240 min. The optimum dose of the adsorbent was 10 g/L, and the equilibrium adsorption capacities of Fe2+ and Mn2+ were 5.645 mg/g and 3.574 mg/g, respectively. The process of IHA/TM adsorption of Fe2+ and Mn2+ in water was spontaneous, endothermic and sustainable, and cooling was not conducive to adsorption. The pseudo-second order kinetic equation can well reflect the adsorption mechanism of IHA/TM on Fe2+ and Mn2+, and the Langmuir adsorption model better describes the isothermal adsorption behaviour. The material characterisation and adsorption experiments indicate that surface coordination and chemical precipitation are the main mechanisms of Fe2+ and Mn2+ removal by IHA/TM.

Effect of nano zinc oxide on proliferation and toxicity of human gingival cells.

BACKGROUND: Periodontal dressing is used to cover the gum surface and protect the wound after periodontal surgery. Nanomaterials have been widely applied in dentistry in recent years. Zinc oxide (ZnO) is one of the main components of periodontal dressing. AIM: This study aims to explore the toxicity ZnO nanoparticles (ZnO NPs) causes to human gingival fibroblast cells (HGF-1) and its effect on cell proliferation. METHODS: First, we identified and analyzed HGF-1, including cell morphology, growth curve, and immunohistochemistry staining. Then, we treated HGF-1 with ZnO NP. Cell viability, the integrity of the cell membrane, oxidative damage, and apoptosis were measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, lactate dehydrogenase (LDH) release assay, fluorescent probe, and flow cytometry. Furthermore, the expression of murine double minute 2 (MDM2) and p53 was determined by quantitative real-time polymerase chain reaction (qPCR) and Western blotting. We finally overexpressed MDM2 in HGF-1 to verify the relationship between MDM2 and cell proliferation. RESULTS: Our research indicated ZnO NPs did not affect cell proliferation at low concentrations. However, high-concentration ZnO NP inhibited cell proliferation, destroyed the integrity of cell membranes, and induced oxidative stress and apoptosis. In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. CONCLUSION: High concentration of ZnO NP caused toxicity to HGF-1 cells and inhibited cell proliferation by regulating MDM2 and p53 expression.

Effect of nano zinc oxide on proliferation and toxicity of human gingival cells.

BACKGROUND: Periodontal dressing is used to cover the gum surface and protect the wound after periodontal surgery. Nanomaterials have been widely applied in dentistry in recent years. Zinc oxide (ZnO) is one of the main components of periodontal dressing. AIM: This study aims to explore the toxicity ZnO nanoparticles (ZnO NPs) causes to human gingival fibroblast cells (HGF-1) and its effect on cell proliferation. METHODS: First, we identified and analyzed HGF-1, including cell morphology, growth curve, and immunohistochemistry staining. Then, we treated HGF-1 with ZnO NP. Cell viability, the integrity of the cell membrane, oxidative damage, and apoptosis were measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, lactate dehydrogenase (LDH) release assay, fluorescent probe, and flow cytometry. Furthermore, the expression of murine double minute 2 (MDM2) and p53 was determined by quantitative real-time polymerase chain reaction (qPCR) and Western blotting. We finally overexpressed MDM2 in HGF-1 to verify the relationship between MDM2 and cell proliferation. RESULTS: Our research indicated ZnO NPs did not affect cell proliferation at low concentrations. However, high-concentration ZnO NP inhibited cell proliferation, destroyed the integrity of cell membranes, and induced oxidative stress and apoptosis. In addition, high concentration of ZnO NPs inhibited the proliferation of HGF-1 by regulating the expression of MDM2 and p53. CONCLUSION: High concentration of ZnO NP caused toxicity to HGF-1 cells and inhibited cell proliferation by regulating MDM2 and p53 expression.

Cyclic drying and wetting tests on combined remediation of chromium-contaminated soil by calcium polysulfide, synthetic zeolite and cement.

Using calcium polysulfide as the reducing agent, synthetic zeolite as the adsorbent, and cement as the curing agent, the dual-index orthogonal test method was used to determine the best remediation dosage of chromium-contaminated soil. On this basis, through the dry-wet cycle test, the durability of the chromium-contaminated soil after repair is analyzed from the perspectives of unconfined compressive strength, toxic leaching concentration, quality loss, and microscopic characterization. Test results showed that the optimal ratio for the joint repair of chromium-contaminated soil was 3 times the amount of CaS5, 15% synthetic zeolite, and 20% cement. With the increase in the number of wet-dry cycles, the unconfined compressive strength of the composite preparation combined to repair chromium-contaminated soil was first increased and then reduced, and the concentration of Cr(VI) and total chromium in the leachate was first decreased and then increased. The higher the chromium content of the contaminated soil was, the lower the unconfined compressive strength, and the higher the leaching concentration of Cr(VI) and total chromium were. With the increase in cycle times, the cumulative mass-loss rate of composite preparations for repairing chromium-contaminated soil gradually increased, and the higher the chromium content was, the higher the cumulative mass-loss rate, which was less than 2%, reflecting the combination of composite preparations for repairing chromium-contaminated soil to have good durability. Microscopic and macroscopic results are consistent with each other.

Preparation, characterization serpentine-loaded hydroxyapatite and its simultaneous removal performance for fluoride, iron and manganese.

Aiming at the problem of excessive fluorine, iron, and manganese pollution in groundwater in mining areas, a serpentine-loaded hydroxyapatite (Srp/HAP) composite adsorbent was prepared by wet chemical coprecipitation. The preparation conditions of the Srp/HAP composite adsorbent were explored, Srp/HAP was microscopically characterized, and the adsorption performance and adsorption mechanism of the Srp/HAP composite adsorbent for F-, Fe2+ and Mn2+ were analyzed. The results showed that the optimal preparation conditions for the composite particles were as follows: solid-liquid ratio of Srp to calcium nitrate solution 20%, aging time 20 h, calcination temperature 180 °C, and calcination time 90 min. Compact Srp/HAP composite adsorbent particles were successfully prepared, and both the lamellar crimp structure of the Srp surface and the problem of HAP surface agglomeration were resolved. After loading, the specific surface area and pore volume of the particles significantly increased, and the surface pore structure improved, which is conducive to the simultaneous adsorption and removal of fluorine, iron and manganese. The optimal reaction conditions for Srp/HAP treatment of composite water samples with F-, Fe2+ and Mn2+ mass concentrations of 5 mg L-1, 20 mg L-1 and 5 mg L-1, respectively, are as follows: dosage of Srp/HAP 3 g L-1, pH 7, temperature 35 °C, and reaction time 150 min. Under these conditions, the removal rates of F-, Fe2+ and Mn2+ were 98.6%, 99.9% and 99.8%, respectively. The quasi-second-order kinetic model and Langmuir isothermal adsorption model described the adsorption process of F-, Fe2+ and Mn2+ by the composite particles well. The adsorption process includes both surface physical adsorption and chemical adsorption. Chemical adsorption is mainly characterized by ion exchange and surface complexation. The Srp/HAP composite particles can be used as an excellent adsorbent for the treatment of groundwater containing fluorine, iron and manganese ions in mining areas.

Roles of ZEB2 and RBM38 in liver cancer stem cell proliferation.

PURPOSE: Liver cancer stem cells are associated with tumor progression, metastasis, and resistance to chemotherapy. Therefore, it is important to understand the proteins that support the tumor microenvironment. The suppression of ZEB2 results from inactivation of the Wnt/ß catenin pathway. Like RBM38, it suppresses tumor outgrowth and helps increase the survival of cancer patients. However, no studies have examined the direct roles of ZEB2 and RBM38 in the tumor microenvironment. METHODS: We developed an early/advanced stage liver cancer mouse model using CD133+ cell injection that mimics liver cancer in all ways. Histology, Western blotting, and immunohistochemistry analyses were used to examine cancer progression. RESULTS: Histologically, the early liver cancer showed microfoci structures; the advanced cancer showed distinct morphological changes with enlarged nucleoli and cell clumping. Immunohistochemical and Western blotting analyses of CD133 and ZEB2 proteins showed similar upregulated expression as the tumor progressed. However, RBM38 expression increased dramatically in early liver cancer but was downregulated in advanced liver cancer. CONCLUSIONS: ZEB2 favors a tumor microenvironment that supports liver cancer stem cell proliferation, while RBM38 expression negatively affects the tumor microenvironment and restricts liver cancer stem cell proliferation.

[Mutation Rate and Clinical Characteristics of CALR, JAK2 V617F and MPL W515K Genes in Patients With Primary Thrombocythemia].

OBJECTIVE: To analyze the mutation rate and clinical characteristics of CALR, MPL W515K and JAK2 V617F genes in patients with primary thrombocythemia (PT). METHODS: Fifty-six patients with PT were selected as the research objects in our hospital. The CALR and MPL W515K gene mutations were determined by genomic DNA-PCR direct sequencing of the PCR products, and the JAK2 V617F gene mutation was detected by allele specific PCR method. RESULTS: Among the 56 patients with PT there were 14 cases of CALR gene mutation with the incidence rate of 25%, including 6 cases of type I, 5 cases of type II and 3 cases of type III. The sex, age, platelet(Plt) count, white blood cell (WBC) count and hemoglobin (Hb) level in the type I case of CALR gene mutation all were not significantly different from that in type II and III(all P>0.05); the WBC level in type III group significantly increased in comparison of type II group (P<0.05), while the sex, age, Hb and Plt levels showed no significant difference between the type III and type II groups (P>0.05). There were 3 cases of MPL W515K gene mutation with the incidence rate of 5.36%; 21 cases of JAK2 V617F gene mutation with the incidence rate of 37.50%. There were 13 cases of CALR gene mutation in negative patients with MPL W515K and JAK2 V617F (18 cases) with 72.22% incidence rate (13/18), and there was no cases of 1 or 2 gene mutations coexisted. The levels of Hb and WBC in peripheral blood of patients with CALR mutation were significantly lower than those of JAK2 V617F mutation (both P<0.05). In 56 cases, there were 3 cases of abnormal karyotype, with the incidence rate of 5.36%. The mutation rate of CALR gene in abnormal karyotypes (66.67%) was significantly higher than that of normal karyotypes (20.75%) (P<0.01). CONCLUSION: The incidence of JAK2 V617F gene mutation increases in the patients with primary thrombocythemia; CALR mutation rate is higher in the patients with negative MPL W515K and JAK2 V617F gene mutation, which may closely correlate with abnormal karyotype; the levels of peripheral Hb and WBC in PT the patients with CALR gene mutation are significantly lower than those in patients with JAK2 V617F mutation.