Role and recent progress of P2Y12 receptor in cancer development.

P2Y12 receptor (P2Y12R) is an adenosine-activated G protein-coupled receptor (GPCR) that plays a central role in platelet function, hemostasis, and thrombosis. P2Y12R activation can promote platelet aggregation and adhesion to cancer cells, promote tumor angiogenesis, and affect the tumor immune microenvironment (TIME) and tumor drug resistance, which is conducive to the progression of cancers. Meanwhile, P2Y12R inhibitors can inhibit this effect, suggesting that P2Y12R may be a potential therapeutic target for cancer. P2Y12R is involved in cancer development and metastasis, while P2Y12R inhibitors are effective in inhibiting cancer. However, a new study suggests that long-term use of P2Y12R inhibitors may increase the risk of cancer and the mechanism remains to be explored. In this paper, we reviewed the structural and functional characteristics of P2Y12R and its role in cancer. We explored the role of P2Y12R inhibitors in different tumors and the latest advances by summarizing the basic and clinical studies on the effects of P2Y12R inhibitors on tumors.

Removal of ciprofloxacin by biosulfurized nano zero-valent iron (BP-S-nZVI) activated peroxomonosulfate: Influencing factors and degradation mechanism.

Agglomeration and passivation restrict the using zero-valent iron nanoparticles (nZVI). Enhancing the reactivity of nZVI is often accomplished by sulfurization. In this work, nZVI was sulfurized using SRB to produce biosulfurized nano zero-valent iron (BP-S-nZVI), which was then utilized as a catalyst to investigating its performance in an advanced oxidation process based on activated peroxomonosulfate (PMS). When the S/Fe was 0.05, 0.4 g/L of catalyst and 0.5 mM PMS were added to a 20 mg/L ciprofloxacin solution. In 120 min, a 90.4% clearance rate was reached. When the initial pH of the solution was within the range of 3-11, all exhibited acceptable degradation performance and were minimally affected by co-existing anions. In this activation system, hydroxyl, superoxide and sulfate radicals (•OH, O2•- and SO4•-, respectively) have been proven to be the main active species. Seven intermediates in the degradation process of CIP were identified by LC-MS analysis and two possible degradation pathways were proposed. In addition, the degradation rate of CIP was still able to reach 87.0% after five cycles, and the removal rate remained unchanged in the CIP solution with actual water samples as background. This study demonstrated that BP-S-nZVI as a catalyst for the activation of PMS for CIP degradation can still show good reactivity, which provides more possibilities for the practical application of BP-S-nZVI in the degradation of pollutants.

Adsorption of lead ions by activated carbon doped sodium alginate/sodium polyacrylate hydrogel beads and their in-situ recycle as sustainable photocatalysts.

In this study, sodium alginate (SA), sodium polyacrylate (PAAS) and powdered activated carbon (PAC) were cross-linked by calcium ions [(Ca(II)] to form SA/PAAS/PAC (SPP) hydrogel beads. The hydrogel-lead sulfide (SPP-PbS) nanocomposites were successfully synthesized by in-situ vulcanization after the lead ions [(Pb(II)] adsorption. SPP showed an optimal swelling ratio (600% at the pH value of 5.0) and superior thermal stability (206 °C of heat-resistance index). The adsorption data of Pb(II) was compatible with the Langmuir model, and the maximum adsorption capacity of SPP was 391.65 mg/g after optimizing the mass ratio of SA to PAAS (3:1). The addition of PAC not only enhanced the adsorption capacity and stability, but also promoted photodegradation. The significant dispersive capacity of PAC and PAAS resulted in PbS nanoparticles with particle sizes of around 20 nm. SPP-PbS showed good photocatalysis and reusability. The degradation rate of RhB (200 mL, 10 mg/L) was 94% within 2 h and maintained above 80% after 5 cycles. The treatment efficiency of SPP was more than 80% in actual surface water. The results of quenching experiments and electron spin resonance (ESR) experiments revealed that the superoxide radicals (O2-) and holes (h+) were the main active species in the photocatalytic process.

Enhanced removal of diclofenac via coupling Pd catalytic and microbial processes in a H2-based membrane biofilm reactor: Performance, mechanism and biofilm microbial ecology.

Diclofenac (DCF) is a most widely used anti-inflammatory drug, which has attracted worldwide attention given its low biodegradability and ecological damage, especially toxic effects on mammals including humans. In this study, a H2-based membrane biofilm reactor (H2-MBfR) was constructed with well-dispersed Pd nanoparticles generated in situ. The Pd-MBfR was applied for catalytic reductive dechlorination of DCF. In batch tests, DCF concentration had significantly effect on the rate and extent DCF removal, and NO3- had negative impact on DCF reductive dechlorination. Over 67% removal of 0.5 mg/L DCF and 99% removal of 10 mg/L NO3--N were achieved in 90 min, and the highest removal of 97% was obtained at 0.5 mg/L DCF in the absence of NO3-. Over 78 days of continuous operation, the highest steady-state removal flux of DCF was 0.0097 g/m2/d. LC-MS analysis indicated that the major product was 2-anilinephenylacetic acid (APA). Dechlorination was the main removal process of DCF mainly owing to the catalytic reduction by PdNPs, microbial reduction, and the synergistic reduction of microbial and PdNPs catalysis using direct delivery of H2. Moreover, DCF reductive Dechlorination shifted the microbial community in the biofilms and Sporomusa was responsible for DCF degradation. In summary, this work expands a remarkable feasibility of sustainable catalytic removal of DCF.

Long-term effects of Cu(II) on denitrification in hydrogen-based membrane biofilm reactor: Performance, extracellular polymeric substances and microbial communities.

Divalent copper (Cu(II)) frequently coexists with nitrate (NO3-) in industrial wastewater and the effect of Cu(II) on the autotrophic denitrification system using H2 as the electron donor remains unknown. In this study, the hydrogen-based membrane biofilm reactor (H2-MBfR) was operated continuously over 150 days to explore the effect of Cu(II) on the performance of autotrophic denitrification system and understand the key roles of EPS and microbial community. More than 95% of 20 mg-N/L NO3- was removed at 1-5 mg/L Cu(II), and the removal rate of NO3--N was stabilized to 82% at 10 mg/L Cu(II) after a short period, while NH4+ and NO2- in effluent were hardly detected, indicated that high concentration of Cu(II) did not permanently inhibit the denitrification performance in H2-MBfR. Colorimetric determination showed that Cu(II) stimulated the secretion of EPS, in which the protein (PN) content was much higher than polysaccharide (PS). The PN/PS ratios increased from 0.93 to 1.99, and the PN was more sensitive to copper invasion. The results of three-dimensional excitation-emission matrix illustrated that tryptophan was the main component of EPS chelating Cu(II) to reduce toxicity. The results of Fourier-transform infrared demonstrated that hydroxyl, carboxyl, and protein amide groups bound and reduced Cu(II). Furthermore, Cu(II) was effectively removed (>80%), and the results of distribution and morphology analysis of Cu(II) show that the electron-dense deposits of monovalent copper (Cu(I)) were found in EPS and biofilms and the reduction of Cu(II) to Cu(I) was an obvious self-defense reaction of biofilm to copper stress. The microbial richness and diversity decreased with the long-term exposure to Cu(II), while the relative abundance of denitrifiers Azospira and Dechloromonas increased. This study provides a scientific basis for the optimal design of treatment system for removal of nitrate and recovery of heavy metals simultaneously.

Microbe-mediated transformation of metal sulfides: Mechanisms and environmental significance.

Microorganisms play a key role in the natural circulation of various constituent elements of metal sulfides. Some microorganisms (such as Thiobacillus ferrooxidans) can promote the oxidation of metal sulfides to increase the release of heavy metals. However, other microorganisms (such as Desulfovibrio vulgaris) can transform heavy metals into metal sulfides crystals. Therefore, insight into the metal sulfides transformation mediated by microorganisms is of great significance to environmental protection. In this review, first, we discuss the mechanism and influencing factors of microorganisms transforming heavy metals into metal sulfides crystals in different environments. Then, we explore three microbe-mediated transformation forms of heavy metals to metal sulfides and their environmental applications: (1) transformation to metal sulfides precipitation for metal resource recovery; (2) transformation to metal sulfides nanoparticles (NPs) for pollutant treatment; (3) transformation to "metal sulfides-microbe" biohybrid system for clean energy production and pollutant remediation. Finally, we further provide critical views on the application of microbe-mediated metal sulfides transformation in the environmental field and discuss the need for future research.

Effects of perfluoroalkyl substances on root and rhizosphere bacteria: Phytotoxicity, phyto-microbial remediation, risk assessment.

BACKGROUND: Per- and polyfluoroalkyl substances (PFAS) is easily sink into soil, affecting plants growth and microenvironment. However, the impacts of PFAS-related risk assessment on root and rhizosphere microbiomes are still poorly understood. OBJECTIVE: Researched on Arabidopsis thaliana and Nicotiana benthamiana growing in contaminated with perfluorooctanoic acid (PFOA), hexafluoropropylene oxide-dimer acid (HFPO-DA) and their mixtures. RESULTS: (i) Bioaccumulation of PFAS in roots was positively correlated with carbon chain length, contamination levels and exposure time, the phytotoxicity was as follows: HFPO-DA < (PFOA + HFPO-DA) < PFOA; (ii) Both short-term and long-term accumulation of PFAS would affect the changes in root antioxidant system and physiological metabolism; (iii) Single or mixed contamination of PFAS had unique influences on rhizosphere microbial diversity, community composition and interspecies interaction, and mixture was more complex. More importantly, the performance of Sphingomonadaceae and Rhizobiaceae microbial communities could contribute to the practice of phyto-microbial soil remediation. FUTURE DIRECTION: Pay more attention on novel pollution pathway in cultivation, exposure levels for different plants (especially crops), as well as more exact and scientific risk assessments. Establish a new PFAS grouping strategy and ecotoxicity life cycle assessment framework.

Carboxymethyl cellulose stabilized ferrous sulfide@extracellular polymeric substance for Cr(VI) removal: Characterization, performance, and mechanism.

Iron-based materials, especially ferrous sulfide (FeS), effectively remediate chromium pollution. However, the agglomeration of FeS reduces its reactivity to chromium. Herein, carboxymethyl cellulose stabilized ferrous sulfide@extracellular polymeric substance (CMC-FeS@EPS) was developed to remove hexavalent chromium (Cr(VI)) from water. CMC-FeS@EPS (98.00%) exhibited excellent removal efficiency of 40 mg/L Cr(VI) than those of FeS (57.35%) and CMC-FeS (68.60%). CMC-FeS@EPS showed good removal efficiency of Cr(VI) in wide pH range (from 4 to 9) and the co-existence of ions. FTIR and XPS results demonstrated that EPS functional group accelerated the process of adsorption and precipitation. Electrochemical results showed that CMC-FeS@EPS transferred electrons to Cr(VI) faster than CMC-FeS. In total, this study started from a new idea of using EPS to improve the performance of CMC-FeS, and provided a simple and effective way to remediate chromium pollution without secondary pollution.

Do perfluoroalkyl substances aggravate the occurrence of obesity-associated glucolipid metabolic disease?

BACKGROUND: Since 2016, more and more studies have been conducted to explore the combination of obesity and perfluoroalkyl substances (PFASs) exposure, and the results indicate that PFASs may be connected with the occurrence of obesity-associated glucolipid metabolic disease (GLMD). OBJECTIVES: This article summarizes the epidemiological studies on PFASs and obesity-related GLMD, as well as relevant experimental evidence. RESULTS: (i) Both obesity and PFASs exposure can cause disorder of glucose and lipid metabolism (GLM). (ii) Obesity is a pivotal factor in the high incidence of GLMD induce by PFASs. (iii) PFASs are aggravating the occurrence of obesity-associated GLMD [e.g., diabetes, cardiovascular disease (CVD), and liver disease]. CONCLUSION: The paper fills the gaps among environmental chemistry/epidemiology/toxicology area research. More importantly, PFASs should be taken into account to explain the high-prevalence of obesity-related GLMD. FUTURE DIRECTION: Three research programs are proposed to explore the synergistic mechanism of PFASs and obesity. In addition, three suggestions are recommended to solve the harm of PFASs pollutants to human beings.

Insight the roles of loosely-bound and tightly-bound extracellular polymeric substances on Cu2+, Zn2+ and Pb2+ biosorption process with Desulfovibrio vulgaris.

The aim of this study is to explore the fate and mechanism of metal cations of biosorption in the Desulfovibrio vulgaris system (including bacterial cells and secreted loosely-bound extracellular polymeric substances (LB-EPS) and tightly-bound extracellular polymeric substances (TB-EPS)). The relative contribution of EPS (TB-EPS and LB-EPS) to the adsorption of three metal cations is much greater than that of bacterial cells, and the adsorption capacity of Pb2+ on EPS (TB-EPS and LB-EPS) is much greater than that of Cu2+ and Zn2+ (Pb2+ > Cu2+ > Zn2+). The order of absorption capacity was as follows: LB-EPS > TB-EPS > bacterial cells, the adsorption contribution of EPS (including TB-EPS and LB-EPS) to Cu2+, Zn2+ and Pb2+ accounted for total adsorption capacity was 82%, 83% and 86%, respectively. It was suggested that LB-EPS was the first reaction barrier of immobilization metal cations before metal cations was able to pass through EPS and react with cells. The adsorption process was dominated by complexation and electrostatic interaction. The three-dimensional excitation-emission matrix (3D-EEM) identified two main fluorescence peaks of the aromatic and tryptophan protein-like substances in EPS. According to the synchronous fluorescence spectra, the tryptophan protein-like substances were gradually quenched with increased metal cations concentrations, which the quencher mechanism is dynamic quenching. The findings of this work are significant to reveal the fate of Cu2+, Zn2+ and Pb2+ during its sorption process onto Desulfovibrio vulgaris, and provide useful information of the interaction between Desulfovibrio vulgaris and its secreted EPS with metal cations.

MiR-140-3p inhibits natural killer cytotoxicity to human ovarian cancer via targeting MAPK1.

Natural killer (NK) cells have pivotal role in immunotherapy of human ovarian cancer (OC). Although microRNAs (miRNAs) participate in dysfunction of NK cells, how and whether miR-140-3p regulates cytotoxicity of NK cells in OC are uncertain. miR-140-3p and mitogen activated protein kinase 1 (MAPK1) abundances were examined via quantitative real-time polymerase chain reaction or western blot. Tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ) abundances were examined via enzyme linked immunosorbent assay. NK cytotoxicity to OC was evaluated via lactate dehydrogenase release. The relevance of miR-140-3p and MAPK1 was proved via luciferase activity analysis. Murine xenograft experiment was applied to assess the function of miR-140-3p on NK cytotoxicity. miR-140-3p was elevated and MAPK1 was declined in NK cells from OC patients, while the levels were reversed after treatment of interleukin-2 (IL-2). MiR-140-3p addition mitigated IFN-γ and TNF-α production induced via IL-2 as well as NK-92 cytotoxicity to OC cells. Additionally, MAPK1 was negatively regulated via miR-140-3p and ablated the influence of miR140-3p on cytotoxicity, cytokines levels. Besides, miR-140-3p enrichment facilitated tumor growth via suppressing function of NK cells in a xenograft model. miR-140-3p suppressed NK cytotoxicity to OC cells via mediating MAPK1, indicating a new avenue of ameliorating NK cells function for OC treatment.

Co-hydrothermal carbonization of food waste-woody biomass blend towards biofuel pellets production.

Co-hydrothermal carbonization of food waste-woody biomass blend was conducted to enhance the pelletization and hydrochar-fuel properties. The hydrochar was characterized by proximate, elemental analysis and HHVs, whilst energy consumption of pelletization, tensile strength, and combustion characteristics of hydrochar pellets were evaluated. Results showed that food waste (FW) blended with 0-50% mainly decreased H/C of hydrochar, while blend ratio from 75% to 100% mainly decreased O/C. When FW blended from 0% to 75%, the energy consumption for hydrochar palletization decreased about 12-17 J, whereas tensile strength of pellets increased about 2.4-5.5 MPa by formation of solid bridge when woody biomass (WS) ratio was increased. The hydrochar pellets from high ratio FW had decreased ignition temperature and maximum weight loss rate with wider temperature range, indicating the increased flammability and moderate combustion. These findings demonstrate that HTC of food waste-woody biomass blend was suitable for pelletization towards solid biofuel production.

Effect of hydrothermal carbonization on storage process of woody pellets: Pellets' properties and aldehydes/ketones emission.

Effect of hydrothermal carbonization (HTC) on the hydrochar pelletization and the aldehydes/ketones emission from pellets during storage was investigated. Pellets made from the hydrochar were stored in sealed apparatuses for sampling. The energy consumption during pelletization and the pellets' properties before/after storage, including dimension, density, moisture content, hardness, aldehyde/ketones emission amount/rate and unsaturated fatty acid amount, were analyzed. Compared with untreated-sawdust-pellets, the hydrochar-pellets required more energy consumption for pelletization, and achieved the improved qualities, resulting in the higher stability degree during storage. The species and amount of unsaturated fatty acids in the hydrochar-pellets were higher than those in the untreated-sawdust-pellets. The unsaturated fatty acids content in the hydrochar-pellets was decreased with increasing HTC temperature. Higher aldehydes/ketones emission amount and rates with a longer emission period were found for the hydrochar-pellets, associated with variations of structure and unsaturated fatty acid composition in pellets.

The effects of temperature and color value on hydrochars' properties in hydrothermal carbonization.

In order to investigate the influence of hydrothermal carbonization (HTC) on the properties of the hydrochars, sawdust with a particle size below 0.45mm was treated in an autoclave at 200-260°C. The physical and chemical characteristics of products were studied, including proximate analysis, elemental composition, fiber content, surface area, bulk density, energy yield, color value, combustion activities and pyrolysis kinetics, etc. It showed that the color of hydrochars turned blacker, greener, and bluer after HTC. The ash, carbon, hydrogen and lignin contents showed a good correlation (R2>0.96) with color coordinates. The decrement in stage 1 and increment in stage 2 of temperature intervals were attributed to the volatile matters removal and fixed carbon accumulation, improving the stability and safety of hydrochars combustion. As shown by the Kissenger-Akahira-Sunose (KAS) and Coats-Redfern calculations, the HTC process can also make the pyrolysis more stable.

Association between a single nucleotide polymorphism in the TP53 region and risk of ovarian cancer.

TP53 is known as a tumor suppressor gene involved in cell cycle regulation. Many previous epidemiological and clinical studies have evaluated the effects of rs1042522 polymorphism on risk of ovarian cancer. But the results are conflicting and heterogeneous. The primary objective of this study was to examine whether rs1042522 polymorphism is associated with ovarian cancer risk. We performed a comprehensive meta-analysis of 19 case-control studies that analyzed rs1042522 polymorphism in ovarian cancer risk. Odds ratios (ORs) were calculated using distinct genetic models. Heterogeneity between studies was detected by the χ(2)-based Q test. Additional analyses such as sensitivity analyses and publication bias were also performed. The rs1042522 polymorphism was not overall associated with ovarian cancer risk. But there was a borderline association in the heterozygote model (OR = 1.09, 95 % CI 0.99-1.21). Similar effects were observed in the subgroup of Caucasian population (the heterozygote model: OR = 1.11, 95 % CI 1.00-1.24). No significant heterogeneity and publication bias were revealed in this meta-analysis. This study provides statistical evidence that TP53 rs1042522 polymorphism may play a role in modulating risk of ovarian cancer. This observation requires further analysis of a larger study size.

Effects of HMGA2 on malignant degree, invasion, metastasis, proliferation and cellular morphology of ovarian cancer cells.

OBJECTIVE: To analyze effects of high mobility group AT-hook 2 (HMGA2) on malignant degree, invasion, metastasis, proliferation and cellular morphology of ovarian cancer cells. METHODS: Three methods were applied to observe the effect on HMGA2 expression in ovarian cancer cells and ovarian epithelial cells. RESULTS: After the application of siRNA-HMGA2, number of T29A2-cell clones was decreased, there was significant difference compared with the negative control Block-iT. After application of let-7c, number of T29A2+ cell clones was decreased significantly, however, after the application of Anti-let-7, the number of clones restored, and there was no significant difference compared with the negative control group. After interference, the number of T29A2- cells which passed through Matrigel polycarbonate membrane were significantly lower than the negative control group. After the treatment of siRNA-HMGA2, let-7c and sh-HMGA2 respectively, growth and proliferation of T29A2-, T29A2+ and SKOV3 were slower, and the phenomenon was most obvious in SKOV3. Stable interference of HMGA2 induced mesenchymal-epithelial changes in the morphology of SKOV3-sh-HMGA2. CONCLUSIONS: HMGA2 can promote malignant transformation of ovarian cancer cells, enhance cell invasion and metastasis, and promote cell growth and proliferation of ovarian cancer cells, which can cause ovarian cancer to progress rapidly and affect the quality of life.