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The transcription factor FOSL1 plays an important role in cell differentiation and tumorigenesis. Primarily, FOSL1 is crucial for the differentiation of several cell lineages, namely adipocytes, chondrocytes, and osteoblasts. In solid tumors, FOSL1 controls the progression of tumor cells through the epithelial–mesenchymal transformation. In this review, we summarize the available data on FOSL1 expression, stabilization, and degradation in the cell. We discuss how FOSL1 is integrated into the intracellular signaling mechanisms and provide a comprehensive analysis of FOSL1 influence on gene expression. We also analyze the pathological changes caused by altered Fosl1 expression in genetically modified mice. In addition, we dedicated a separate section of the review to the role of FOSL1 in human cancer. Primarily, we focus on the FOSL1 expression pattern in solid tumors, FOSL1 importance as a prognostic factor, and FOSL1 perspectives as a molecular target for anticancer therapy.

The peroxisome proliferator-activated receptor PPAR-γ is one of three PPAR nuclear receptors that act as ligand-activated transcription factors. In immune cells, the skin, and other organs, PPAR-γ regulates lipid, glucose, and amino acid metabolism. The receptor translates nutritional, pharmacological, and metabolic stimuli into the changes in gene expression. The activation of PPAR-γ promotes cell differentiation, reduces the proliferation rate, and modulates the immune response. In the skin, PPARs also contribute to the functioning of the skin barrier. Since we know that the route from identification to the registration of drugs is long and expensive, PPAR-γ agonists already approved for other diseases may also represent a high interest for psoriasis. In this review, we discuss the role of PPAR-γ in the activation, differentiation, and proliferation of skin and immune cells affected by psoriasis and in contributing to the pathogenesis of the disease. We also evaluate whether the agonists of PPAR-γ may become one of the therapeutic options to suppress the inflammatory response in lesional psoriatic skin and decrease the influence of comorbidities associated with psoriasis.

Recently, significant attention has been drawn to carbon materials containing cobalt coordinated to nitrogen, as the promising inexpensive catalysts of a wide range of applications. Given that non-oxidative propane dehydrogenation to propylene (PDH) is also becoming increasingly important, we present the results on PDH over Co-N-C/SiO2 composites. The latter were prepared by pyrolysis of silicone gel enriched with Co(II) salt and triethanolamine. According to XRD, HRTEM and XPS characterizations, the resulting materials consist of metallic cobalt nanoparticles of about 5 to 10 nm size and subnano-sized cobalt species (cobalt single atom sites coordinated to nitrogen/carbon), which are uniformly distributed in mesoporous silica of high specific surface area (up to 500 m2 g−1). The composites demonstrated significant catalytic activity in PDH, which was examined under typical reaction conditions (600 °C, 1 atm) using a fixed bed flow reactor. The subnano-sized Co centers proved to be the real active catalytic sites responsible for the target reaction, while carbon deposition induced by Co nanoparticles provided the catalyst deactivation. It is shown that the catalyst can be reactivated by the treatment with oxygen, which, in addition, notably increases selectivity to propylene (up to 98%) and enhances the catalyst stability in the next operation cycle. This remarkable change in catalytic behavior is shown to be due to the dramatic structural modification of the catalyst upon high-temperature oxidation.

These lecture notes provide a fresh approach to investigating singularly perturbed systems using asymptotic and geometrical techniques.It gives many examples and step-by-step techniques, which will help beginners move to a more advanced level.

The paper outlines the method of forming mathematical models for the dynamic interaction of the vibroactive technological equipment with load-bearing structures of industrial structures on the basis of discrete-continual approximations previously developed by the author. Ways of implementing methods in the formation of vibration protection systems of structures are provided in the paper. The features of systems’ functioning and their sensitivity to fluctuating vibration frequency processes are also described.

Alcohols (bioalcohols) is a class of chemicals that are used as a feedstock for the manufacturing of a large number of valuable intermediates in industrially important processes. Currently, sustainable technologies for selective conversion of alcohols utilize “green” oxidants, mainly, ambient air or oxygen. Due to the high affinity of oxygen towards silver, the latter serves as an active component of supported heterogeneous catalysts. In this review, we consider Ag-based catalysts that participate in gas- or liquid-phase oxidation of alcohols. Oxidation of methanol, ethanol, ethylene glycol, propylene glycol, glycerol, benzyl and allyl alcohols is mostly considered. A particular attention is paid to selective photooxidation of alcohols over Ag-based catalysts. We discuss the catalyst composition in terms of (1) the state of the active component, (2) the nature of the substrate, (3) support nature, and (4) the strength of the metal–support interactions.

In order to develop highly efficient and stable catalysts for oxygen reduction reaction (ORR) that do not contain precious metals, it is necessary to modify carbon nanotubes (CNT) and define the effect of the modification on their activity in the ORR. In this work, the modification of CNTs included functionalization by treatment in NaOH or HNO3 (soft and hard conditions, respectively) and subsequent doping with nitrogen (melamine was used as a precursor). The main parameters that determine the efficiency of modified CNT in ORR are composition and surface area (XPS, BET), hydrophilic–hydrophobic surface properties (method of standard contact porosimetry (MSP)) and zeta potential (dynamic light scattering method). The activity of CNT in ORR was assessed following half-wave potential, current density within kinetic potential range and the electrochemically active surface area (SEAS). The obtained results show that the modification of CNT with oxygen-containing groups leads to an increase in hydrophilicity and, consequently, SEAS, as well as the total (overall) current. Subsequent doping with nitrogen ensures further increase in SEAS, higher zeta potential and specific activity in ORR, reflected in the shift of the half-wave potential by 150 mV for CNTNaOH-N and 110 mV for CNTHNO3-N relative to CNTNaOH and CNTHNO3, respectively. Moreover, the introduction of N into the structure of CNTHNO3 increases their corrosion stability.

Formic acid (FA) can easily be decomposed, affording molecular hydrogen through a controllable catalytic process, thus attaining great importance as a convenient hydrogen carrier for hydrogen energetics. Supported gold nanoparticles are considered to be among the most promising catalysts for such applications. However, questions remain regarding the influence of the catalyst support on the reaction selectivity. In this study, we have examined the catalytic activity of typical gold catalysts, such as Au/TiO2, Au/SiO2, and Au/Al2O3 in decomposition of FA, and then compared it with the catalytic activity of corresponding supports. The performance of each catalyst and support was evaluated using a gas-flow packed-bed reactor. It is shown that the target reaction, FA → H2 + CO2, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA → H2O + CO, results exclusively from the acid-base behavior of supports.

The microheterogeneous model makes it possible to describe the main transport properties of ion-exchange membranes using a single set of input parameters. This paper describes an adaptation of the microheterogeneous model for describing the electrical conductivity and diffusion permeability of a track-etched membrane (TEM). Usually, the transport parameters of TEMs are evaluated assuming that ion transfer occurs through the solution filling the membrane pores, which are cylindrical and oriented normally to the membrane surface. The version of the microheterogeneous model developed in this paper takes into account the presence of a loose layer, which forms as an intermediate layer between the pore solution and the membrane bulk material during track etching. It is assumed that this layer can be considered as a “gel phase” in the framework of the microheterogeneous model due to the fixed hydroxyl and carboxyl groups, which imparts ion exchange properties to the loose layer. The qualitative and quantitative agreement between the calculated and experimental concentration dependencies of the conductivity and diffusion permeability is discussed. The role of the model input parameters is described in relation to the structural features of the membrane. In particular, the inclination of the pores relative to the surface and their narrowing in the middle part of the membrane can be important for their properties.

The effect of nitrogen doped bamboo-like carbon nanotubes (N–CNTs) on the properties of supported platinum (0.2 and 1 wt %) catalysts in formic acid decomposition for hydrogen production was studied. It was shown that both impregnation and homogeneous precipitation routes led to the formation of electron-deficient platinum stabilized by pyridinic nitrogen sites of the N–CNTs. The electron-deficient platinum species strongly enhanced the activity and selectivity of the Pt/N–CNTs catalysts when compared to the catalysts containing mainly metallic platinum nanoparticles. A comparison of bamboo-like N–CNTs and herring-bone nitrogen doped carbon nanofibers (N–CNFs) as the catalyst support allowed us to conclude that the catalytic properties of supported platinum are determined by its locally one-type interaction with pyridinic nitrogen sites of the N–CNTs or N–CNFs irrespective of substantial structural differences between nanotubes and nanofibers.