gef Gene Expression in MCF-7 Breast Cancer Cells is Associated with a Better Prognosis and Induction of Apoptosis by p53-Mediated Signaling Pathway

Breast cancer research has developed rapidly in the past few decades, leading to longer survival times for patients and opening up the possibility of developing curative treatments for advanced breast cancer. Our increasing knowledge of the biological pathways associated with the progression and development of breast cancer, alongside the failure of conventional treatments, has prompted us to explore gene therapy as an alternative therapeutic strategy. We previously reported that gef gene from E. coli has shown considerable cytotoxic effects in breast cancer cells. However, its action mechanism has not been elucidated. Indirect immunofluorescence technique using flow cytometry and immunocytochemical analysis were used to detect breast cancer markers: estrogen (ER) and progesterone (PR) hormonal receptors, human epidermal growth factor receptor-2 proto-oncogene (c-erbB-2), ki-67 antigen and p53 protein. gef gene induces an increase in ER and PR expressions and a decrease in ki-67 and c-erbB-2 gene expressions, indicating a better prognosis and response to treatment and a longer disease-free interval and survival. It also increased p53 expression, suggesting that gef-induced apoptosis is regulated by a p53-mediated signaling pathway. These findings support the hypothesis that the gef gene offers a new approach to gene therapy in breast cancer.     

Proton conducting polymer blends from poly(2,5‐benzimidazole) and poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid)

Proton conducting polymer electrolyte membranes were produced by blending of poly(2,5‐benzimidazole) (ABPBI) and poly(2‐acrylamido‐2‐methyl‐1‐propanesulfonic acid) (PAMPS) at several stoichiometric ratios with respect to polymer repeating units. The membranes were characterized by using Fourier transform infrared spectroscopy for interpolymer interactions and scanning electron microscope for surface morphology. Thermal stability of the materials was investigated by thermogravimetric analysis. Glass transition temperatures of the samples were measured via differential scanning calorimetry. The spectroscopic measurements and water uptake studies indicate a complexation between ABPBI and PAMPS that inhibited polymer exclusion up on swelling in excess water. Proton conductivities of the anhydrous and humidified samples were measured using impedance spectroscopy. The proton conductivity of the humidified ABPBI:PAMPS (1 : 2) blend showed a proton conductivity of 0.1 S/cm, which is very close to Nafion 117, at 20°C at 50% relative humidity. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Optimization of some parameters of stirred mill for ultra-fine grinding of refractory Au/Ag ores

In this study, optimization of some parameters of stirred mill on ultra-fine grinding of refractory Au/Ag ores was performed. A three-level Box-Behnken design combining a response surface methodology (RSM) with quadratic programming (QP) was employed for modelling and optimization of some operating parameters in ultra-fine grinding. Grinding tests were carried out in a laboratory scale pin-type vertical stirred mill. The relationship between the response, i.e. d₈₀ size, and four grinding parameters, i.e. ball diameter, grinding time, ball charge ratio and stirrer revolution was presented as empirical model equations. Analysis of variance showed a high coefficient of determination value (R² = 0.9698), thus ensuring a satisfactory of the second-order regression model with the experimental data.The model equations were then optimized using the quadratic programming method to minimize for d₈₀ size within the experimental range studied. The optimum conditions were found to be 1.61 mm for ball diameter, 11.50 min for grinding time, 80% for ball charge ratio and 745 rpm for stirrer revolution for this grinding process.In order to verify the improvement of grinding performance using the optimal level of control factors three verification experiments were conducted, and the results for d₈₀ was 3.37 μm, which were smaller than those obtained in the initial tests.     

Insights into the Adhesive Mechanisms of Tree Frogs using Artificial Mimics

Elastic, microstructured surfaces (hydrophobic and hydrophilic) mimicking the surface structure of tree‐frog toe‐pads are fabricated. Their adhesion and friction behaviour in the presence of a liquid layer is evaluated and compared to flat controls. Tree‐frog‐like patterns are beneficial for wet adhesion only if the liquid does not wet the surface. The situation is different in friction, where the surface structure lead to significantly higher friction forces only if the liquid does wet the surface. Taking into account that tree‐frog attachment pads are hydrophilic and that their secretion wets all kind of surfaces, our results indicate that the surface structure in tree‐frog toe‐pads has been developed for climbing, when shear (friction) forces are involved. These results evidence the benefits and limitations of the surface design (microstructure and hydrophilicity) for adhesion and friction under wet conditions.     

Highly porous starch/poly(ethylene‐alt‐maleic anhydride) composite nanofiber mesh

In this study, starch‐based hybrid electrospun nanofiber meshes were fabricated by electrospinning. Spinning solutions were prepared by mixing starch and certain amounts of poly(ethylene‐alt‐maleic anhydride). Starch‐based nanofiber meshes became insoluble in water with thermal‐induced esterification of hydroxyl groups onto starch backbone. Morphologic and structure analysis of the electrospun nanofiber meshes were investigated by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques. Thermal properties of nanofiber meshes were characterized by thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC). Thermal stability of nanofiber meshes were increased with formation of intermolecular bonds between starch and poly(ethylene‐alt‐maleic anhydride). POLYM. COMPOS. 34:1321–1324, 2013. © 2013 Society of Plastics Engineers     

Thermal,mechanical and water adsorption properties of corn starch–carboxymethylcellulose/methylcellulose biodegradable films

The objective of this study was to investigate the effect of the addition of methylcellulose and carboxymethylcellulose on the thermal, mechanical and water adsorption properties of starch-based films plasticized with glycerol or polyethylene glycol (PEG). Mechanical tests showed that as the methylcellulose and carboxymethylcellulose proportion increased, starch films became more resistant to break, resulting in higher TS values. Besides there has been a positive effect on the elasticity of starch films realized by a considerable increase in E% values. Depending on the plasticizer type, either single or dual glass transitions were seen in DSC thermograms. One glass transition temperature was observed for films plasticized with glycerol, on the contrary, dual glass transitions were detected for PEG plasticized films. This behavior was attributed to the phase separation of the PEG. In addition, the presence of an endothermic peak in the thermograms of PEG plasticized films was taken as another indicator of the phase separation. As a result, it was suggested that PEG was not as compatible as glycerol with the composite polysaccharide matrix and plasticizer type was the main factor that shaped the thermal profiles of the film samples. Water adsorption isotherm data showed that samples displayed nonlinear sorption profile which is typical for hydrophilic films. In all films tested, equilibrium moisture contents, increased almost linearly up to a a_w of 0.65–0.85, beyond where a sharp increase was noted. Adsorption data was adequately fitted by BET and GAB models. Eventually, it can be concluded that film forming properties of starch can be improved by incorporation of methylcellulose and carboxymethylcellulose to the polymer matrix.     

Modulatory effects of yerba maté (Ilex paraguariensis) on the PI3K‐AKT signaling pathway

The aim of this study was to evaluate the effects of yerba maté (YM) extract on the phosphatidylinositol 3‐kinase (PI3K)‐AKT signaling pathway in vivo. The mice were introduced to either standard‐ or high‐fat diet (HFD). After 8 weeks on an HFD, mice were randomly assigned to one of the two treatment conditions, water or yerba maté extract at 1.0 g/kg. After treatment, glucose blood level and hepatic insulin response were evaluated. Liver tissue was examined to determine the mRNA levels using the PI3K‐AKT PCR array. The nuclear translocation of forkhead box O1 (FOXO1) was determined by an electrophoretic mobility‐shift assay. Our data demonstrated that yerba maté extract significantly decreased the final body weight, glucose blood levels, and insulin resistance of mice. Molecular analysis demonstrated that an HFD downregulated Akt2, Irs1, Irs2, Pi3kca, Pi3kcg, and Pdk1; after yerba maté treatment, the levels of those genes returned to baseline. In addition, an HFD upregulated Pepck and G6pc and increased FOXO1 nuclear translocation. The intervention downregulated these genes by decreasing FOXO1 nuclear translocation. The results obtained demonstrate for the first time the specific action of yerba maté on the PI3K‐AKT pathway, which contributed to the observed improvement in hepatic insulin signaling.     

CO2, GDP and RET: An aggregate economic equilibrium analysis for Turkey

There is a worldwide interest in renewable electricity technologies (RETs) due to growing concerns about global warming and climate change. As an EU candidate country whose energy demand increases exponentially, Turkey inevitably shares this common interest on RET. This study, using an aggregate economic equilibrium model, explores the economic costs of different policy measures to mitigate CO₂ emissions in Turkey. The model combines energy demands, capital requirements and labor inputs at a constant elasticity of substitution under an economy-wide nested production function. Growing energy demand, triggered by economic growth, is met by increased supply and initiates new capacity additions. Investment into RET is encouraged via the incorporation of (a) endogenous technological learning through which the RET cost declines as a function of cumulative capacity, and (b) a willingness to pay (WTP) function which imposes the WTP of consumers as a lower bound on RET installation. The WTP equation is obtained as a function of consumer income categories, based on data gathered from a pilot survey in which the contingent valuation methodology was employed. The impacts of various emission reduction scenarios on GDP growth and RET diffusion are explored. As expected, RET penetration is accelerated under faster technological learning and higher WTP conditions. It is found that stabilizing CO₂ emissions to year 2005 levels causes economic losses amounting to 17% and 23% of GDP in the years 2020 and 2030, respectively.     

Immobilization of laccase onto poly(glycidylmethacrylate) brush grafted poly(hydroxyethylmethacrylate) films: Enzymatic oxidation of phenolic compounds

Poly(hydroxyethylmethacrylate), p(HEMA) films were prepared via UV-initiated photo-polymerization. After activation of the hydroxyl groups of p(HEMA) by bromination, surface-initiated atom transfer radical polymerization (ATRP) of glycidylmethacrylate was conducted in dioxane/bipyridine mixture with CuBr as catalyst at 65 °C. The epoxy groups of the poly(glycidylmethacrylate) brushes were converted into amino groups with the reaction of ammonia. The modified p(HEMA-g-GMA)-NH₂ films were used as an ion-exchange support for the immobilization of laccase. The influence of pH and initial laccase concentration on the immobilization capacity of the p(HEMA-g-GMA)-NH₂ films has been investigated. The amount of immobilized laccase on the p(HEMA-g-GMA)-NH₂ films was determined as 139 μg/cm² films. The recovered activity of the immobilized laccase on the fibrous polymer grafted films was about 71% compared to free enzyme. The maximum activity (V_max) and Michealis constant (K_m) of laccase immobilized on the films, were found to be 15.4 U/mg and 23 mM, respectively. Finally, the immobilized laccase was operated in a batch system for enzymatic oxidation of phenol, p-chlorophenol and aniline.     

Functionalization in solution of polypropylene with a maleinized hyperbranched polyol polyester: Structural,thermal, rheological,and mechanical properties

The functionalization of polypropylene (PP) with a maleinized hyperbranched polyester polyol (MHBP) was performed in solution to obtain PP-g-MHBPs. The degree of functionalization (FD) increased with MHBP and dicumyl peroxide (DCP) contents, but the contact angle followed an opposite behavior. The sample obtained with the proportion of 9.0 wt % MHBP and 2.0 wt % DCP and presented the highest FD value. An FD value of 2.4 wt %, produced a reduction of 19° on the contact angle. It was observed by differential scanning calorimetry (DSC) that the PP-g-MHBPs obtained by employing 3.0 wt % of MHBP, exhibited a slight reduction of the melting temperature (T_m) with the increase in the amounts of FD and DCP. Some FD values obtained in this study are higher than those obtained both commercial and noncommercial grades of PP functionalized with maleic anhydride. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46932.