Source-sink relationships of anthropogenic metal(loid)s from urban catchment to waterway in relation to spatial pattern of urban green infrastructures.

Surface sediment in urban waterways originates from fine topsoil particles within catchments via surface erosion, often bonded with non-degradable metal(loid)s. This study posited that urban green infrastructures (UGIs) can influence anthropogenic metal(loid) transport from catchment topsoil to waterway sediment by retaining moveable particles. In multiply channeled downtown Suzhou, China, UGIs' spatial patterns were examined in relations to metal(loid)s source (catchment topsoil) - sink (waterway surface sediment) dynamics. Anthropogenic metal(loid)s - As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn - were spatially quantified in sediment at 144 waterway points and in topsoil at 154 UGIs' points across 7 subwatersheds. Integrated metal(loid) loads revealed significantly higher sediment loads (except for As) than topsoil, varying with element specificity and spatial unmatching across the subwatersheds. Loads of metal(loid)s in topsoil showed no significant differences among UGI types, but sediment loads of As, Cr, and Ni correlated positively with topsoil loads in roadside and public facility UGIs within 100 m- and 200 m-wide riparian buffer zones. However, waterfront UGIs negatively impacted on these correlations for Cr, Hg, and Ni loads within the riparian buffer zones. These findings highlight metal(loid) specificity and UGIs' spatial pattern effects on anthropogenic metal(loid) loads between catchment topsoil (source) and waterway surface sediment (sink), offering valuable guidelines for UGIs' design and implementation.

Amlodipine inhibits the proliferation and migration of esophageal carcinoma cells through the induction of endoplasmic reticulum stress.

BACKGROUND: L-type calcium channels are the only protein channels sensitive to calcium channel blockers, and are expressed in various cancer types. The Cancer Genome Atlas database shows that the mRNA levels of multiple L-type calcium channel subunits in esophageal squamous cell carcinoma tumor tissue are significantly higher than those in normal esophageal epithelial tissue. Therefore, we hypothesized that amlodipine, a long-acting dihydropyridine L-type calcium channel blocker, may inhibit the occurrence and development of esophageal cancer (EC). AIM: To investigate the inhibitory effects of amlodipine on EC through endoplasmic reticulum (ER) stress. METHODS: Cav1.3 protein expression levels in 50 pairs of EC tissues and corresponding paracancerous tissues were examined. Subsequently, the inhibitory effects of amlodipine on proliferation and migration of EC cells in vitro were detected using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide and Transwell assays. In vivo experiments were performed using murine xenograft model. To elucidate the underlying mechanisms, in vitro cell studies were performed to confirm that ER stress plays a role in inhibition proliferation and migration of EC cells treated with amlodipine. RESULTS: The expression level of Cav1.3 in esophageal carcinoma was 1.6 times higher than that in paracancerous tissues. Amlodipine treatment decreased the viability of esophageal carcinoma cells in a dose- and time-dependent manner. In vivo animal experiments also clearly indicated that amlodipine inhibited the growth of EC tumors in mice. Additionally, amlodipine reduces the migration of tumor cells by inhibiting epithelial-mesenchymal transition (EMT). Mechanistic studies have demonstrated that amlodipine induces ER stress-mediated apoptosis and suppresses EMT. Moreover, amlodipine-induced autophagy was characterized by an increase in autophagy lysosomes and the accumulation of light chain 3B protein. The combination of amlodipine with the ER stress inhibitor 4-phenylbutyric acid further confirmed the role of the ER stress response in amlodipine-induced apoptosis, EMT, and autophagy. Furthermore, blocking autophagy increases the ratio of apoptosis and migration. CONCLUSION: Collectively, we demonstrate for the first time that amlodipine promotes apoptosis, induces autophagy, and inhibits migration through ER stress, thereby exerting anti-tumor effects in EC.

Implications of obstructive sleep apnea in lung adenocarcinoma: A valuable omission in cancer prognosis and immunotherapy.

Lung adenocarcinoma (LUAD) is a highly invasive malignant tumor with poor prognosis, and there is growing evidence that obstructive sleep apnea (OSA) could significantly promotes the risk of LUAD. In order to improve the treatment outcomes of patients with LUAD and OSA, we aim to screen OSA-related genes that may potentially affect LUAD and to discover a high sensitivity prognostic signature that can stratify LUAD/OSA patients and to further accurately identify LUAD patients who might respond to immunotherapy. Molecular subtypes classified by the prognostic signature did not belong to any previously reported subtypes of LUAD. The tumor microenvironment (TME), mutation, and so on, were significantly distinct between patients within different risk groups or clusters. Combined with gene set variation analysis (GSVA) and drug susceptibility analysis, patients in the low-risk group (The vast majority of patients belonging to cluster2 by molecular subtyping) were not suitable for immunotherapy due to T-cell exhaustion caused by long-term inflammatory response; the question of how to reverse T-cell exhaustion may be a primary consideration. Cluster3 patients had the highest benefit from immunotherapy, and although cluster1 patients had the worst prognosis, they were more sensitive to traditional chemotherapeutic drugs. Animal experiments showed that chronic intermittent hypoxia (CIH) could not only significantly promote the tumor growth of LUAD, but also increase the expression levels of risk genes. This risk model may contribute greatly to the evaluation of prognosis, molecular characteristics, and treatment modalities of LUAD/OSA, and could be further translated into clinical applications to ameliorate the treatment dilemmas.

Spatial effects of urban green infrastructure on instream water quality assessed by chemical and sensory indicators.

Urban green infrastructure has been simulated effectively and economically to reduce volume and pollutants of stormwater runoffs but its spatial effects remain unclear. A snap sampling campaign was carried out for surface water quality in the downtown waterway network of a pilot sponge city (Suzhou) in China, dividing into 7 subwatersheds according to the digital elevation map. In total, 144 sampling points were investigated and measured for chemical quality of surface water while 68 out of the sampling points had a sensory evaluation questionnaire interview for water quality with 321 respondents, in whom the native residents scored a significant spatiality of water quality. The downtown waterway network had phosphorus-limited eutrophic surface water with total nitrogen worse than Class V of the national guidelines. Chemical and sensory evaluation indexes of surface water quality had significant spatial consistency (p < 0.001). All types of green spaces (%) in subwatershed, especially along the urban waterway network (waterfront) and roadside, and in the 100 m riparian buffer zone, significantly influenced nutrient loads in surface water. Findings of the present study suggest that the 100 m riparian buffer zone would be priority areas and the waterfront and roadside should be the highly efficient spots for planning strategy on urban green infrastructure implementation to reduce nutrient loads in surface water and to improve urban landscape aesthetics.

[Effects of TOFA on growth of Eca109 and KYSE-450 cells in human esophageal squamous cell carcinoma].

Objective: To investigate the effects of 5-tetradecanoxy 2-furanic acid (TOFA) on cell proliferation, cell cycle and apoptosis of esophageal squamous cell carcinoma (ESCC) cells. Methods: Eca-109 cells and KYSE-450 cells were divided into control group (DMSO) and experimental group (TOFA), respectively. The cells (4×103 cells/100 µl) were inoculated into 96-well plates with 5 multiple wells at each concentration. After 24 h culture, cells were treated with DMSO or different concentrations (1, 3, 5, 10 µg/ ml) of TOFA for 24, 48 and 72 h. Cell proliferation was detected by MTT, cell cycle and apoptosis were detected by flow cytometry, the expression levels of p21 and Cleaved caspase-3 and modification levels of p-Akt, p-mTOR and p-4EBP1 were detected by Western blot, and intracellular free fatty acids were detected by special kits. Results: MTT results showed that TOFA inhibited the proliferation of Eca109 and KYSE-450 cells in a concentration and time dependent manner (all P<0.05), with IC50 of 4.65 µg/ml and 3.93 µg/ml for 48 h, respectively. Flow cytometry results showed that compared with DMSO group, the percentage of cells in G2/M phase was increased and the apoptosis rate was increased in the experimental group. Western blotting results showed that compared with DMSO group, p21 and Cleaved caspase-3 protein expression levels were up-regulated, and p-AKT, p-mTOR and p-4EBP1 protein expression levels were down-regulated (all P<0.05). Conclusion: TOFA inhibits the proliferation, blocks the cycle progression and promotes apoptosis of ESCC, the mechanism may be related to the AKT/mTOR/4EBP1 signaling pathway.

Trichostatin A promotes esophageal squamous cell carcinoma cell migration and EMT through BRD4/ERK1/2-dependent pathway.

BACKGROUND: Histone deacetylases (HDACs) have been demonstrated to be aberrantly activated in tumorigenesis and cancer development. Thus, HDAC inhibitors (HDACIs) are considered to be promising anti-cancer therapeutics. However, recent studies have shown that HDACIs promote the migration of many cancer cells. Therefore, there is a need to elucidate the underlying mechanisms of HDACIs on cancer cell migration to establish a combination therapy that overcomes HDACI-induced cell migration. METHODS: KYSE-150 and EC9706 cells were treated differently. Effects of drugs and siRNA treatment on tumor cell migration and cell signaling pathways were investigated by transwell migration assy. Gene expression for SNAI2 was tested by RT-qPCR. Western blot analysis was employed to detect the level of E-cadherin, ß-catenin, vimentin,Slug，ERK1/2, H3, PAI-1 and BRD4. The effect of drugs on cell morphology was evaluated through phase-contrast microscopic images. RESULTS: TSA promotes epithelial-mesenchymal transition (EMT) in ESCC cells by downregulating the epithelial marker E-cadherin and upregulating mesenchymal markers ß-catenin, vimentin, Slug, and PAI-1. Knockdown of Slug by siRNA or inhibition of PAI-1 clearly suppressed TSA-induced ESCC cell migration and resulted in the reversal of TSA-triggered E-cadherin, ß-catenin, and vimentin expression. However, no crosstalk between Slug and PAI-1 was observed in TSA-treated ESCC cells. Blocking ERK1/2 activation also inhibited TSA-induced ESCC cell migration, EMT, and upregulation of Slug and PAI-1 levels in ESCC cells. Interestingly, inhibition of BRD4 suppressed TSA-induced ESCC cell migration and attenuated TSA-induced ERK1/2 activation and upregulation of Slug and PAI-1 levels. CONCLUSIONS: Our data indicate the existence of at least two separable ERK1/2-dependent signaling pathways in TSA-mediated ESCC cell migration: an ERK1/2-Slug branch and an ERK1/2-PAI-1 branch. Both branches of TSA-induced ESCC cell migration appear to favor the EMT process, while BRD4 is responsible for two separable ERK1/2-dependent signaling pathways in TSA-mediated ESCC cell migration.

Trichostatin A augments esophageal squamous cell carcinoma cells migration by inducing acetylation of RelA at K310 leading epithelia-mesenchymal transition.

Protein acetylation modification controlled by acetyltransferases (HATs) and histone deacetylases (HDACs) regulates multiple biologic processes including cell proliferation and migration. HDAC inhibitors (HDACi) are currently used as a promising epigenetic-based therapy for cancer treatment. Of the anticancer activity, accumulating evidence has shown that HDACi can enhance cell migration in subset of cancer cells. Thus, there is a critical need to identify such counter anticancer activity to HDACi in different cancer cell types and elucidate the rational in order to develop appropriate combination therapies in cancer treatment. In seeking to address the effect of HDACi on esophageal squamous cell carcinoma (ESCC) cells migration, trichostatin A (TSA), a canonical HDACi targeting class I and class II HDACs, was used. Here, we report the discovery that TSA augmented ESCC cells migration by increasing the acetylation of nuclear factor-κB/RelA at lysine 310 (K310). To elucidate the mechanism by which TSA promotes the migration of ESCC cells, plasmid of RelA K310R, a mutant precluding acetylation at K310, was transfected into ESCC cells. Blocking acetylation of RelA at K310 significantly arrogated TSA-induced cell migration. Mechanistic investigations revealed that TSA increased the level of acetylated RelA at K310 (RelA K310ac), thereby increasing the level of epithelia-mesenchymal transition (EMT) transcription factor slug mRNA, which in turn induced EMT. Overall, this study indicates that TSA promotes ESCC cells migration by RelA K310ac-slug-EMT pathway. Our findings provide a strategy to eradicate HDACi-induced ESCC cells migration by targeting RelA as a combination therapy with nonspecific HDACi in ESCC treatment.

[Influence of Substrate Exposure Level on ANAMMOX Microbial Activity and Biomass].

Substrate exposure levels are vital for the growth and metabolism of ANAMMOX microorganisms, and their effects on growth characteristics of ANAMMOX sludge during the enrichment process have been rarely reported. Using two continuous flow stirred reactors and the process of a gradually developing nitrogen load, the changes in biomass and activity, as well as nitrogen removal efficiency of the reactors were investigated under high substrate exposure level culture mode (R1:effluent NH4+-N and NO2--N concentrations were 40-60 mg·L-1) and low substrate exposure level culture mode (R2:effluent NH4+-N and NO2--N concentrations were 0-20 mg·L-1). The results showed that the high substrate exposure level culture mode was more beneficial to the improvement of nitrogen removal performance of the ANAMMOX reactor. For comparison, the NLR (nitrogen load rate), which was 0.69 kg·(m3·d)-1, and the NRR (nitrogen remove rate), which was up to 0.41 kg·(m3·d)-1, was obtained in the high substrate exposure culture mode. These values were twice as high as those obtained in the low substrate exposure culture mode. Under the culture mode with high substrate exposure level, the sludge concentration (in VSS) and the total gene copy numbers of ANAMMOX reached 1805 mg·L-1 and 4.81×1012 copies, respectively, which was conducive to the rapid enrichment of ANAMMOX microorganisms. In the low substrate exposure level culture mode, ANAMMOX sludge was more active,in N/VSS, 0.27 g·(g·d)-1, which was conducive to the cultivation of ANAMMOX sludge with higher biological activity.

MicroRNA­212 facilitates the motility and invasiveness of esophageal squamous carcinoma cells.

As a tumor­associated microRNA (miR), miR­212 has dual functions; either as an oncogene or a tumor suppressor. A high expression level of miR­212 was reported to be associated with poor outcome in patients with esophageal squamous cell carcinoma (ESCC), however, its role in ESCC progression has not been explored. In the present study, an in vitro cell model of lentivirus­mediated gain­of­function demonstrated promotion of ESCC cell migration and invasion when miR­212 was overexpressed, and no effect on cell proliferation. miR­212 resulted in downregulation of the expression of E­cadherin, ß­catenin, vimentin and Twist1. Moreover, it led to increased levels of extracellular matrix (ECM)­degrading enzymes, matrix metalloproteinase­9 and urokinase­type plasminogen activator. Furthermore, berberine inhibited miR­212­induced ESCC cell migration, unlike the PI3K inhibitor LY294002, rapamycin (mTOR inhibitor), 5­(Tetradecyloxy)­2­furoic acid (TOFA; an acetyl­CoA carboxylase 1 inhibitor), metformin and propranolol. These data suggest that miR­212 activates multiple signaling cascades and facilitates ESCC cell motility and invasion by promoting the epithelial­mesenchymal transition and degrading the ECM. Berberine may be a potential therapeutic agent against metastasis in patients with ESCC, who express high levels of miR­212.

[Effect of Temperature and pH on Nitrogen Conversion in Feammox Process].

In recent years, the oxidation of NH4+ using Fe(Ⅲ) as an electron acceptor under anaerobic conditions (Feammox) has received significant research attention. In this study, the effect of pH and temperature on nitrogen conversion during the Feammox process was studied through activity recovery of Feammox sludge acclimated by anaerobic ammonium oxidation (ANAMMOX) sludge. Results showed that after 40 d operation, activity of Feammox sludge was recovered. There was evident ammonia nitrogen conversion and total nitrogen removal from the environment, and the products were mainly nitrate and nitrogen. The concentration of nitrite remained below 2 mg·L-1. pH value and temperature significantly influenced nitrogen transformation during the Feammox process. With pH value of 7 and temperature of 30℃ during the Feammox process, the removal rate of total nitrogen was relatively high (>50%). When the pH value was 6.5, the conversion rate of ammonia nitrogen was 80.2%. During the Feammox reaction process, precipitation of iron ion compounds and coating on the sludge surface were the main interference factors leading to continuous operation of the reactor and exploration of the reaction mechanism.

[Analysis of CANON Process Start-up with Fiber Carrier].

A CANON reactor with fiber carrier was started up by seeding nitrification sludge and ANAMMOX sludge to study the operating characteristics of a fiber carrier. The results showed that total nitrogen removal load rose from 0.09 kg·(m3·d)-1 to 0.9 kg·(m3·d)-1 and remained steady in the 85th day. This indicated that fiber carrier is beneficial to the accumulation of sludge, and the reactor can maintain a higher biomass. The DO in the reactor reached 5 mg·L-1 with the enrichment of microorganisms, biofilm thickening, and the improvement of the reactor's ability. The DO gradient of the biofilm from the outside to the inside was 0.32-0 mg·L-1, which could be obtained by a microelectrode. It was shown that the permeability of oxygen to the biofilm decreased, and the amount of nitrifying microorganisms decreased with biofilm thickening. The quantitative PCR results showed that the abundance of ANAMMOX was an order of magnitude more than before. The abundance of AOB increased slightly, while the abundance of NOB stayed at a relatively low level.

[Inhibitory Effects of Phosphate and Recovery on a Nitrification System].

The effect of phosphate concentration on nitrification was studied by using a stabilization nitrosation system, which was started up in a continuous flow reactor by inoculating sludge from a municipal wastewater treatment plant. The results showed that the nitrification system was started successfully after operating for 14 days. The conversion rate of ammonia nitrogen reached 92.2%, the nitrite accumulation rate was 73.66%, and the nitrite generation rate was 14.42 g·(m3·d)-1. There was no effect of phosphate concentration on the nitrosation system between 10 and 30 mg·L-1; and the conversion rate of ammonia nitrogen was decreased with the continuous increase in phosphate concentration. When the concentration of phosphate was 80 mg·L-1, with an ammonia conversion rate 13.6%, accumulation rate of nitrite of 18.19%, and nitrite generation rate of 0.54 g·(m3·d)-1, the reaction was severely inhibited. After reducing the influent phosphate concentration to 0, with the ammonia nitrogen conversion rate at more than 80%, nitrite accumulation rate improved to 86.96%, and the nitrite generation rate being 15.63 g·(m3·d)-1, the system recovered after operating for 14 days.

Promote quantitative ischemia imaging via myocardial perfusion CT iterative reconstruction with tensor total generalized variation regularization.

Myocardial perfusion computed tomography (MPCT) imaging is commonly used to detect myocardial ischemia quantitatively. A limitation in MPCT is that an additional radiation dose is required compared to unenhanced CT due to its repeated dynamic data acquisition. Meanwhile, noise and streak artifacts in low-dose cases are the main factors that degrade the accuracy of quantifying myocardial ischemia and hamper the diagnostic utility of the filtered backprojection reconstructed MPCT images. Moreover, it is noted that the MPCT images are composed of a series of 2/3D images, which can be naturally regarded as a 3/4-order tensor, and the MPCT images are globally correlated along time and are sparse across space. To obtain higher fidelity ischemia from low-dose MPCT acquisitions quantitatively, we propose a robust statistical iterative MPCT image reconstruction algorithm by incorporating tensor total generalized variation (TTGV) regularization into a penalized weighted least-squares framework. Specifically, the TTGV regularization fuses the spatial correlation of the myocardial structure and the temporal continuation of the contrast agent intake during the perfusion. Then, an efficient iterative strategy is developed for the objective function optimization. Comprehensive evaluations have been conducted on a digital XCAT phantom and a preclinical porcine dataset regarding the accuracy of the reconstructed MPCT images, the quantitative differentiation of ischemia and the algorithm's robustness and efficiency.

[Granular Characteristics of Anaerobic Ammonia Oxidation Sludge During the Recovery Process].

Operation instability has become one of the factors restricting the application of the anaerobic ammonia oxidation (ANAMMOX) process. Under the condition that the substrate is not suppressed, the effects of the substrate concentration on the granulation and activity of ANAMMOX granular sludge in the recovery process were studied by restoring the activity of ANAMMOX sludge, which was derived from early-stage operation instability of the continuous stirred tank reactor (CSTR). The results show that the activity of ANAMMOX sludge was recovered and the denitrification capacity increased significantly after 126 days of operation. When the NH4+-N and NO2--N concentrations were 450 mg·L-1 and 560 mg·L-1, respectively, the nitrogen removal was achieved in both the high-and low-substrate concentration reactors and the maximum NRR was 16.97 kg·(m3·d)-1 and 14.43 kg·(m3·d)-1, respectively. With the improvement of the nitrogen removal capacity of the reactor (the granular diameter of the sludge is increased), the extracellular polymeric substance (EPS) content increased in both reactors from 34.45 to 77.52 and to 94.18 mg·g-1, respectively, and the PN/PS increased from 1.89 to 6.25 and 6.84, respectively. To a certain extent, the increase of PN/PS is conducive to the granulation of ANAMMOX sludge, but a too large PN/PS would lead to the instability of granular sludge and sludge loss.

Berberine displays antitumor activity in esophageal cancer cells in vitro.

AIM: To investigate the effects of berberine on esophageal cancer (EC) cells and its molecular mechanisms. METHODS: Human esophageal squamous cell carcinoma cell line KYSE-70 and esophageal adenocarcinoma cell line SKGT4 were used. The effects of berberine on cell proliferation were evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. For cell cycle progression, KYSE-70 cells were stained with propidium iodide (PI) staining buffer (10 mg/mL PI and 100 mg/mL RNase A) for 30 min and cell cycle was analyzed using a BD FACSCalibur flow cytometer. For apoptosis assay, cells were stained with an Annexin V-FITC/PI apoptosis detection kit. The rate of apoptotic cells was analyzed using a dual laser flow cytometer and estimated using BD ModFit software. Levels of proteins related to cell cycle and apoptosis were examined by western blotting. RESULTS: Berberine treatment resulted in growth inhibition of KYSE-70 and SKGT4 cells in a dose-dependent and time-dependent manner. KYSE-70 cells were more susceptible to the inhibitory activities of berberine than SKGT4 cells were. In KYSE-70 cells treated with 50 µmol/L berberine for 48 h, the number of cells in G2/M phase (25.94% ± 5.01%) was significantly higher than that in the control group (9.77% ± 1.28%, P < 0.01), and berberine treatment resulted in p21 up-regulation in KYSE-70 cells. Flow cytometric analyses showed that berberine significantly augmented the KYSE-70 apoptotic population at 12 and 24 h post-treatment, when compared with control cells (0.83% vs 43.78% at 12 h, P < 0.05; 0.15% vs 81.86% at 24 h, P < 0.01), and berberine-induced apoptotic effect was stronger at 24 h compared with 12 h. Western blotting showed that berberine inhibited the phosphorylation of Akt, mammalian target of rapamycin and p70S6K, and enhanced AMP-activated protein kinase phosphorylation in a sustained manner. CONCLUSION: Berberine is an inhibitor of human EC cell growth and could be considered as a potential drug for the treatment of EC patients.

[Ammoniac Waste Gas in-situ Treatment Based on ANAMMOX Process].

The feasibility of ammoniac waste gas in-situ treatment by partial nitrification(PN)-anaerobic ammonia oxidation(ANAMMOX) reactor was studied. The PN-ANAMMOX reactor was successfuly started up after 60 d operation in conditions of low dissolved oxygen control(0.2 mg·L-1), pH 7.9-8.2 and temperature(30-35℃). The total nitrogen removal efficiency reached 88% and the nitrogen removal rate increased from 0.05 kg·(m3·d)-1 to 0.7 kg·(m3·d)-1. In the treatment of ammoniac waste gas, the excess oxygen in it would lead to massive growth of nitrifying bacteria, when the ammonia concentration was lower than 2.59%. The ammonia and oxygen in waste gas met the requirement of the reactor for nitrogen removal, when the ammonia concentration stayed between 2.59% and 4.2%. Extra air flow was required for reactor oxygen supplement when the ammonia concentration was higher than 4.2%. The ammonia removal efficiency reached 100%, the total nitrogen removal efficiency reached 90.06%, while the total nitrogen removal rate was 0.51 kg·(m3·d)-1 after 60 day operation for ammoniac waste gas purification. It is indicated that the integrated reactor based on PN-ANAMMOX process can achieve stable removal of ammonia waste gas.

[Removal of Nitrogen from Alcohol Wastewater by PN-ANAMMOX].

An integrated partial nitrification anaerobic ammonia oxidation reactor was used to explore the feasibility of nitrogen removal from recycled ethanol wastewater. The results show that the integrated partial nitrification-anaerobic ammonia oxidation (PN-ANAMMOX) reactor was started successfully after 40 d under the conditions of pH 7.8±0.5, temperature 30-35℃, and aerobic ORP value 120-150 mV. The total nitrogen removal rate of 0.125 kg·(m3·d)-1 increased to 0.75 kg·(m3·d)-1, Inoculation of mature nitrosated biofilms and anaerobic ammonium oxide granules can accelerate the start of the reactor. The effects of alcohol wastewater on the PN-ANAMMOX reactor were mainly caused by biodegradable TOC, The biodegradable TOC concentration of 100mg·L-1 in alcohol wastewater can reduce the removal rate of total nitrogen from 0.75 kg·(m3·d)-1 to 0.25 kg·(m3·d)-1,this inhibition can be restored. Different concentrations of alcohol wastewater were dosed into the PN-ANAMMOX reactor to acclimate the bacteria. The total nitrogen removal rate first decreased and then increased, as the influent concentration gradient increased, which was beneficial for improving the efficiency of nitrogen removal by extending the HRT and increasing the dissolved oxygen in the PN stage. Finally, the nitrogen removal rate stabilized at 0.65 kg·(m3·d)-1. These results show that PN-ANAMMOX can be used for the treatment of alcohol wastewater.

[Start-up and Capacity Enhancement of a Partial Nitrification Pilot Reactor in Continuous Flow].

The continuous flow reactor was used to treat simulated ammonia nitrogen wastewater by inoculating the sludge after filtration and adding a suspended filler. Regulations of free ammonia (FA), free nitrous acid (FNA), and dissolved oxygen (DO) in the reactor were the key to achieving a successful start-up of the pilot scale nitrosation reactor. The results show that the enrichment of ammonium oxidizing bacteria (AOB) and the elimination of nitrite oxidizing bacteria (NOB) are achieved by adjusting the operational mode of high DO, low DO, FA, and FNA in the reactor operation. The nitrite production rate (NPR) in the reactor was 1.27 kg·(m3·d)-1 and the nitrogen accumulation rate (NAR) was stable at 98% at the end of the start-up period. qPCR was used to study the difference in the functional microorganisms (AOB, NOB) between the beginning and the end of the start-up period. The results show that the copy number of microbial AOB grew from 5.3×109 copies·mL-1 to 1.6×1011 copies·mL-1. The copy number of NOB decreased from 1.1×1010 copies·mL-1 to 1.2×109 copies·mL-1, because of the joint regulation of DO, FA, FNA to suppress NOB.

[Influence of Phosphate on Nitrogen Removal Efficiency of ANAMMOX Sludge].

In this study, the effect of phosphate concentration on the nitrogen removal efficiency of ANAMMOX sludge was researched. The inhibition kinetic parameters were fitted and the abundance of ANAMMOX bacteria in the reactor before and after phosphate inhibition was analyzed by Real-time PCR. The short-term experiments showed that there was no significant effect on the nitrogen removal efficiency of ANAMMOX sludge when phosphate concentration was less than 30mg·L-1. With the increase of influent phosphate concentration, the removal rate of nitrogen decreased rapidly. When the phosphate concentration was raised to 200mg·L-1, the activity of ANAMMOX sludge reached a complete inhibition state. The parameters of phosphate inhibition were fitted by Haldane inhibition model. The half-inhibition constant was 70.1 mg·L-1. The long-term results showed that when the phosphate concentration was less than 50 mg·L-1, the effect on the nitrogen removal efficiency of ANAMMOX sludge was not significant. When the phosphate concentration reached 70-90 mg·L-1, The activity of ANAMMOX sludge was obviously affected, and the stability could be restored after a certain period. Increasing the phosphate concentration had a more significant effect and resulted in a longer recovery time. Finally, when the concentration of phosphate reached 100 mg·L-1, the nitrogen removal efficiency of ANAMMOX was seriously inhibited. The rate of nitrogen removal decreased from 158.33 g·(m3·d)-1 to 60.17 g·(m3·d)-1, resulting in 62% inhibition. The results of real-time PCR showed that the concentration of ANAMMOX was decreased from (9.97±0.86)×107 cells·mL-1 to (8.26±0.54)×107 cells·mL-1 in the restraining sludge system, and there was a relatively reduced trend.

High DEPTOR expression correlates with poor prognosis in patients with esophageal squamous cell carcinoma.

OBJECTIVE: The disheveled, Egl-10, and pleckstrin (DEP) domain containing mammalian target of rapamycin (mTOR)-interacting protein (DEPTOR) is a binding protein containing mTOR complex 1 (mTORC1), mTOR complex 2 (mTORC2), and an endogenous mTOR inhibitor. DEPTOR shows abnormal expressions in numerous types of solid tumors. However, how DEP-TOR is expressed in esophageal squamous cell carcinoma (ESCC) remains elusive. METHODS: The expression of DEPTOR in 220 cases of ESCC and non-cancerous adjacent tissues was detected by immunohistochemistry. DEPTOR levels in ESCC and paired normal tissue were quantified using reverse transcription-polymerase chain reaction and Western blot analysis to verify the immunohistochemical results. The relationship between DEPTOR expression and the clinicopathological features of ESCC was analyzed based on the results of immunohistochemistry. Finally, we analyzed the relationship between DEPTOR expression and the prognosis of patients with ESCC. RESULTS: Immunohistochemical staining showed that the expression rate of DEPTOR in ESCC tissues was significantly increased. DEPTOR mRNA and protein expression was significantly higher in ESCC tissues than in normal adjacent esophageal squamous tissues. High DEPTOR expression was significantly correlated with regional lymph node status in the TNM stage of patients with ESCC. Kaplan-Meier survival curves showed that the rate of overall survival was significantly lower in patients with high DEPTOR expression than in those with low DEPTOR expression. Additionally, high DEPTOR expression was an independent prognostic predictor for ESCC patients. CONCLUSION: High DEPTOR expression is an independent prognostic biomarker indicating a worse prognosis for patients with ESCC.