Removal and kinetics of cadmium and copper ion adsorption in aqueous solution by zeolite NaX synthesized from coal gangue.

Zeolite can remove the heavy metals in wastewater, but the removal efficiency was determined by the types of zeolites and the treatment conditions. In this study, a kind of zeolite NaX synthesized from the coal gangue, a by-product of coal production, was used and the removal efficiency of Cd2+ and Cu2+and the kinetic models were studied. The effects of its dosage, initial pH value of wastewater, and adsorption temperature on its adsorption of heavy metals Cd2+ and Cu2+ in the simulated wastewater were studied through the indoor experiments in laboratory, and the adsorption mechanism was analyzed by the adsorption kinetic model based on its adsorption efficiency and its structures. The results show that the zeolite NaX synthesized from coal gangue has a good adsorption effect on Cd2+ and Cu2+. The adsorption reaches the best effect when the dosage of zeolite is 2 g/L, the initial pH of simulated wastewater is 5, the adsorption temperature is room temperature (25 ℃), and the removal efficiency of Cd2+ and Cu2+ (100 mg/L) is more than 90%. Additionally, the Langmuir, Freundlich, and Temkin isothermal adsorption models were used to compare and analyze the adsorption effects. The equilibrium data was better fitted by the Langmuir model with the maximum adsorption capacities of 100.11 mg/g (Cd2+) and 95.29 mg/g (Cu2+), and both separation coefficients were 0-1, which shows that the process was the favorable adsorption. Weber Morris diffusion model shows that the adsorption process at 120 min was more consistent with the pseudo-second-order kinetics model, and the adsorption efficiency was simultaneously controlled by the liquid diffusion step and intraparticle diffusion step. Moreover, the removal mechanism of Cd2+ and Cu2+ mainly includes physical adsorption and ion exchange. Therefore, the adsorption effect of zeolite synthesized from coal gangue is remarkable, which will provide a feasible and potential alternative for its resource application.

Circ_0016760 Serves as a Cancer Promoter in Non-small Cell Lung Cancer Through miR-876-3p/NOVA2 Axis.

Non-small cell lung cancer (NSCLC) is a serious threaten to human health globally. Circular RNAs (circRNAs) were testified to alter the progression of NSCLC. This work intended to investigate the functional role of circ_0016760 in NSCLC development and the potential mechanism. Expression of circ_0016760, microRNA (miR)-876-3p and NOVA alternative splicing regulator 2 (NOVA2) was determined via quantitative reverse transcription-PCT (qRT-PCR) or western blotting. Cell viability, clonogenicity and apoptosis were assessed by Cell Counting Kit-8 (CCK-8) assay, colony formation assay and flow cytometry, respectively. Transwell assay was performed to examine cell migration and invasion. Western blotting was also conducted to detect the levels of epithelial-to-mesenchymal transition (EMT)-related proteins. Role of circ_0016760 in vivo was evaluated via xenograft model assay. Moreover, the interaction between miR-876-3p and circ_0016760 or NOVA2 was verified by dual-luciferase reporter assay or RNA Immunoprecipitation (RIP) assay. Circ_0016760 and NOVA2 were upregulated, while miR-876-3p expression was decreased in NSCLC tissues and cells. Circ_0016760 depletion suppressed NSCLC cell proliferation and metastasis in vitro, as well as hampered tumor growth in vivo. Circ_0016760 acted as a sponge of miR-876-3p, and miR-876-3p could target NOVA2. Circ_0016760 might play vital roles in NSCLC by regulating miR-876-3p/NOVA2 axis. Circ_0016760 could promote the malignant development of NSCLC through miR-876-3p/NOVA2 axis, at least in part.

LYAR Promotes Colorectal Cancer Progression by Upregulating FSCN1 Expression and Fatty Acid Metabolism.

Colorectal cancer (CRC) is a highly malignant tumor associated with poor prognosis, yet the molecular mechanisms are not fully understood. In this study, we showed that LYAR, a nucleolar protein, is expressed at a higher level in CRC tissue than in adjacent normal tissue and that LYAR expression is closely associated with distant CRC metastasis. LYAR not only significantly promotes the migration and invasion of CRC cells in vitro, but knockdown (KD) of LYAR in CRC cells also inhibits xenograft tumor metastasis in vivo. Microarray analysis of LYAR KD cells combined with a chromatin immunoprecipitation (ChIP) assay, gene reporter assay, and rescue experiment indicated that FSCN1 (encoding fascin actin-bundling protein 1 (Fascin-1)) serves as a novel key regulator of LYAR-promoted migration and invasion of CRC cells. Knockdown of FSCN1 significantly inhibits subcutaneous tumorigenesis of CRC cells and leads to the downregulation of FASN and SCD, genes encoding key enzymes in fatty acid synthesis. In summary, this study reveals a novel mechanism by which LYAR promotes tumor cell migration and invasion by upregulating FSCN1 expression and affecting fatty acid metabolism in CRC.

Discovery of chalcone-modified estradiol analogs as antitumour agents that Inhibit tumour angiogenesis and epithelial to mesenchymal transition.

Angiogenesis plays an essential role in tumourigenesis and tumour progression, and anti-angiogenesis therapies have shown promising antitumour effects in solid tumours. 2-Methoxyestradiol (2ME2), an endogenous metabolite of estradiol, has been regarded as a potential antitumour agent mainly targeting angiogenesis. Here we synthesized a novel series of chalcones based on 2-methoxyestradiol and evaluated their potential activities against tumours. Compound 11e was demonstrated to have potent antiangiogenic activity. Further studies showed that 11e suppressed tumour growth in human breast cancer (MCF-7) xenograft models without obvious side effects. Evaluation of the mechanism revealed that 11e targeted the epithelial to mesenchymal transition (EMT) process in MCF-7 cells and inhibited HUVEC migration and then contributed to hindrance of angiogenesis. Thus, 11e may be a promising antitumour agent with excellent efficacy and low toxicity.

LncRNA UCA1 sponges miR-26a to regulate the migration and proliferation of vascular smooth muscle cells.

BACKGROUND: Recent studies have shown that the long non-coding RNA urothelial carcinoma-associated (UCA1) plays a key role in cardiovascular injury. However, the potential biological role of UCA1 in progression of atherosclerosis (AS) remains unclear. The aim of the present study is to identify the regulation of lncRNA UCA1 on atherosclerosis-related vascular dysfunction via miR-26a targeting phosphatase and tensin homolog (PTEN), and investigate the underlying mechanisms in the development of atherosclerosis. METHODS: The proliferation and migration were detected using CCK-8 assay, Wound healing assay and Transwell assay. The expression of miR-26a and its target gene in vascular smooth muscle cells was detected by qRT-PCR, the complementary binging of miRNA and lncRNA was verified by luciferase assays. PTEN was predicted to be the target of miR-26a and the prediction was verified by luciferase assays. RESULTS: Expression of miR-26a was up-regulated in ox-LDL (50 mg/l) induced vascular smooth muscle cell (VSMCs), and overexpression of miR-26a inhibited PTEN expression and promoted PCNA α-SMA and SM22-α expression (qRT-PCR and WB). CONCLUSION: The expression of UCA1 antagonized the effect of miR-26a on the downregulation of its target PETN and contraction phenotype. This study reveals that lncRNA UCA1 act as an endogenous sponge of miR-26a and downregulates miR-26a expression levels, and thereby relieving the inhibition of its target gene PTEN and alleviates VSMCs proliferation against atherosclerosis.

Combination therapy of hTERTR and FAM96A for hepatocellular carcinoma through enhancing apoptosis sensitivity.

Avoidance of apoptosis induced by anticancer drugs is an essential factor of carcinogenesis and a hallmark of resistance to cancer therapy. Human telomerase reverse transcriptase receptor (hTERTR) is a potential anti-cancer agent for inhibiting tumor growth. Family with sequence similarity 96 member A (FAM96A) is a ubiquitous, conserved protein and possesses apoptosome-activating and pro-apoptotic tumor suppressor potential in hepatocellular carcinoma (HCC). In the present study, hTERTR and FAM96A were identified as efficient anti-cancer agents for activating apoptosomes and reducing tumor growth. The potential tumor suppressor function of combination treatment with hTERTR and FAM96A in HCC was also investigated. hTERTR and FAM96A proteins were expressed by genetic engineering and their anti-cancer function was explored in vitro and in vivo. Effects of hTERTR and FAM96A on improvement of apoptotic sensitivity and inhibition of migration and invasion were examined in cancer cells and in a mouse model. The present results demonstrated that the therapeutic effects of hTERTR and FAM96A were effective for inhibiting tumor growth and inducing apoptosis of HCC cells in H22-bearing nude mice compared with single agent treatment. hTERTR and FAM96A were found to bind with apoptotic protease activating factor 1 and human telomerase reverse transcriptase, which enhanced the apoptosis of tumor cells and apoptosis sensitivity. In addition, hTERTR and FAM96A therapy enhanced cytotoxic effects by cytotoxic T lymphocyte responses, interferon-γ release, T lymphocytes infiltration and apoptosis on tumor cells. Furthermore, hTERTR and FAM96A protein inhibited tumor growth in HCC mice. In conclusion, the present findings suggested that combination therapy with hTERTR and FAM96A may serve as novel tumor suppressor agents.

[Response of water quality to agricultural cultivation in Liangwanghe River catchment of Fuxianhu Lake region].

Response of water quality to agricultural cultivation was investigated for the Liangwanghe River catchment of Fuxianhu Lake region in Yunnan Province of China. Two typical tillage lands-the rice-wheat rotation (R-W) and the tobacco-pea (T-P) rotation were selected and monitored. Groundwater quality and water quality of Liangwanghe River were monitored simultaneously, as well as the farmland cultivation situation at that time. It was found that cultivation activities, such as transplanting, base fertilizer applying, top dressing, draining would cause apparent elevation of concentrations of TP, PO4(3-)-P, TN, NO3(-)-N and NH4(+)-N of groundwater in a short time period. Nutrients adsorption by crops during different bearing periods has an obvious relationship to the change of contents of TP, PO4(3-)-P, TN, NO3(-)-N, and NH4(+)-N in groundwater in a long time scale. When the crops are in a peak demand for nutrients, contents of nutrients in groundwater were found to reduce obviously, and contents of nutrients may rise for other crop conditions. Contents of TP and PO4(3-)-P of Liangwanghe River for full cultivation periods were found to be 5.8% and 21.7% lower than those for partial cultivation periods, while contents of TN, NH4(+)-N and NO3(-)-N for full cultivation periods were found to be 11.5%, 242.6% and 9.55% higher than those for partial cultivation periods.