Cancer stem cells-driven tumor growth and immune escape: the Janus face of neurotrophins

Cancer Stem Cells (CSCs) are self-renewing cancer cells responsible for expansion of the malignant mass in a dynamic process shaping the tumor microenvironment. CSCs may hijack the host immune surveillance resulting in typically aggressive tumors with poor prognosis. In this review, we focus on neurotrophic control of cellular substrates and molecular mechanisms involved in CSC-driven tumor growth as well as in host immune surveillance. Neurotrophins have been demonstrated to be key tumor promoting signaling platforms. Particularly, Nerve Growth Factor (NGF) and its specific receptor Tropomyosin related kinase A (TrkA) have been implicated in initiation and progression of many aggressive cancers. On the other hand, an active NGF pathway has been recently proven to be critical to oncogenic inflammation control and in promoting immune response against cancer, pinpointing possible pro-tumoral effects of NGF/TrkA-inhibitory therapy. A better understanding of the molecular mechanisms involved in the control of tumor growth/immunoediting is essential to identify new predictive and prognostic intervention and to design more effective therapies. Fine and timely modulation of CSCs-driven tumor growth and of peripheral lymph nodes activation by the immune system will possibly open the way to precision medicine in neurotrophic therapy and improve patient's prognosis in both TrkA- dependent and independent cancers

Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts

The kinetics of the electrochemical oxidation of graphite to volatile compounds by electrolysing molten bisulphates in the temperature range from 180 to 320°C has been studied by conventional steady-state and non-steady-state measurements. CO2, CO and traces of SO2 are formed during the electrochemical reaction. Assuming 4 Faraday/mol of CO2, the anodic efficiency is about 90%. The CO2/CO ratio is about 2 and is independent of the cd in the range considered. The electrochemical reaction is compared to the thermal oxidation of graphite. The reaction is interpreted through a scheme involving consecutive reactions, where the rate-determining step, under Temkin conditions, is a thermal process involving a desorption of intermediates following either a first-order or second-order process depending on the type of adsorption obeyed. The activation energy derived from the rate constant at the rest potential is about 42·5 Kcal/mol.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Electrochemical oxidation of iodide dissolved in sodium-nitrate-potassium-nitrate eutectic melt on a platinum rotating disk electrode

The E/I curve related to the electrochemical oxidation of iodide dissolved in molten nitrates on a platinum rotating disk electrode involves two anodic waves. The first corresponds to a reversible two-electron process and the second to a reversible one-electron process. A definite ratio between the anodic limiting currents is established suggesting that the second anodic wave is not independent from the first one. The parameters related to the diffusion of the species participating in the reaction are evaluated.Les courbes de polarisation concernant l'oxydation électrochimique de l'iodure dissous dans des nitrates fondus sur une électrode à disque tournant de platine comprend deux ondes anodiques. La première appartient a un procèssus réversible de deux électrons et la deuxième à un procèssus réversible d'un seul électron. Une relation définie est établie entre les courants limites anodiques, indiquent que la deuxième onde anodique n'est pas indépendante de la première. Les paramètres relatifs à la diffusion des espèces qui participent à la réaction sont évalués.Die E/I-Kurven, die bei der elektrochemischen Oxydation von in geschmolzenen Nitraten gelöstem Jodid an einer rotierenden Scheibenelektrode aus Platin auftreten, umfassen zwei anodische Wellen. Die erste entspricht einem reversiblen Zweielektronen- und die zweite einem reversiblen Einelektronenprozess. Es wird ein genaues Verhältnis zwischen den anodischen Grenztrömen aufgestellt unter der Annahme, dass die zweite anodische Welle von der ersten nicht unabhängig ist. Es werden die Diffusionsparameter der Reaktionsteilnahmer angegeben.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Synthesis, Characterization and Electrocatalytic Activity of Bi- and Tri-metallic Pt-Based Anode Catalysts for Direct Ethanol Fuel Cells

Three Pt-based anode catalysts supported on Vulcan XC-72R (VC) were prepared by using a modified polyol process. These materials were characterized and tested by X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF) and Transmission Electron Microscopy (TEM). XRD and TEM analysis indicated that especially the ternary anode catalysts consisted of uniform nanosized particles with sharp distribution. The Pt lattice parameter was smaller, in the ternary PtSnIr catalyst whereas it increased with the addition of Sn and Rh, in the corresponding binary and ternary catalysts. Cyclic voltammetry (CV) measurements showed that Sn, Ir and Rh may act as promoter of Pt enhancing ethanol electro-oxidation activity. It was found that the direct ethanol fuel cell (DEFC) performances were significantly improved with these modified anode catalysts. This effect on the DEFC performance is attributed to the so-called bi-tri-functional mechanism and to the electronic interaction between Pt and additives. The performance increased significantly with the temperature. However, it was also possible to observe some decay with time for all catalysts due to the formation of surface poisons, probably consisting in CO-like species. At 60 °C, the PtSnIr catalyst showed the best performance, as a result of a proper morphology and promoting effectFil: D'Urso, C.. Centro Nazionale della Ricerca. ITAE; ItaliaFil: Bonesi, Alejandro Roberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico la Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata; ArgentinaFil: Triaca, Walter Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico la Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata; ArgentinaFil: Castro Luna Berenguer, Ana Maria del Carmen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico la Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata; ArgentinaFil: Baglio, V.. Centro Nazionale della Ricerca. ITAE; Italia; ItaliaFil: Aricò, A. S.. Centro Nazionale della Ricerca. ITAE; Italia; Itali

Synthesis, Characterization and Electrocatalytic Activity of Bi- and Tri-metallic Pt-Based Anode Catalysts for Direct Ethanol Fuel Cells

Three Pt-based anode catalysts supported on Vulcan XC-72R (VC) were prepared by using a modified polyol process. These materials were characterized and tested by X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF) and Transmission Electron Microscopy (TEM). XRD and TEM analysis indicated that especially the ternary anode catalysts consisted of uniform nanosized particles with sharp distribution. The Pt lattice parameter was smaller, in the ternary PtSnIr catalyst whereas it increased with the addition of Sn and Rh, in the corresponding binary and ternary catalysts. Cyclic voltammetry (CV) measurements showed that Sn, Ir and Rh may act as promoter of Pt enhancing ethanol electro-oxidation activity. It was found that the direct ethanol fuel cell (DEFC) performances were significantly improved with these modified anode catalysts. This effect on the DEFC performance is attributed to the so-called bi-tri-functional mechanism and to the electronic interaction between Pt and additives. The performance increased significantly with the temperature. However, it was also possible to observe some decay with time for all catalysts due to the formation of surface poisons, probably consisting in CO-like species. At 60 °C, the PtSnIr catalyst showed the best performance, as a result of a proper morphology and promoting effectFacultad de Ciencias ExactasInstituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Synthesis, Characterization and Electrocatalytic Activity of Bi- and Tri-metallic Pt-Based Anode Catalysts for Direct Ethanol Fuel Cells

Three Pt-based anode catalysts supported on Vulcan XC-72R (VC) were prepared by using a modified polyol process. These materials were characterized and tested by X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF) and Transmission Electron Microscopy (TEM). XRD and TEM analysis indicated that especially the ternary anode catalysts consisted of uniform nanosized particles with sharp distribution. The Pt lattice parameter was smaller, in the ternary PtSnIr catalyst whereas it increased with the addition of Sn and Rh, in the corresponding binary and ternary catalysts. Cyclic voltammetry (CV) measurements showed that Sn, Ir and Rh may act as promoter of Pt enhancing ethanol electro-oxidation activity. It was found that the direct ethanol fuel cell (DEFC) performances were significantly improved with these modified anode catalysts. This effect on the DEFC performance is attributed to the so-called bi-tri-functional mechanism and to the electronic interaction between Pt and additives. The performance increased significantly with the temperature. However, it was also possible to observe some decay with time for all catalysts due to the formation of surface poisons, probably consisting in CO-like species. At 60 °C, the PtSnIr catalyst showed the best performance, as a result of a proper morphology and promoting effectFacultad de Ciencias ExactasInstituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Electrochemical and Scanning Force Microscopy Characterization of Fractal Palladium Surfaces Resulting from the Electroreduction of Palladium Oxide Layers

Pd oxide layers were grown by applying to smooth Pd electrodes a potential reversal technique (PRT) in 1 M H2SO4 at 25 °C. The electroreduction of the Pd oxide layer was made either voltammetrically or potentiostatically, yielding a Pd overlayer with a large increase in surface area. The effective range of PRT conditions for increasing the Pd surface area was established. The increase in surface area of treated Pd was voltammetrically determined. The electrochemical behavior of treated Pd electrodes in acid revealed an enhancement of the H atom surface electroadsorption processes. This behavior is consistent with the fractal characteristics of the treated Pd electrode surface, as demonstrated by the analysis of scanning force microscopy imaging data.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

Success rate of palatal orthodontic implants: a prospective longitudinal study

AIM: The purpose of this prospective cohort study was to assess the survival and success rates of palatal implants. MATERIAL AND METHODS: Seventy patients (56 female, 14 male; age 25-6 +/- 10-8 years) receiving Orthosystem (Straumann AG, Basel, Switzerland) palatal implants from March 1999 to November 2006 were included. The indication was established according to the required anchorage for orthodontic therapy. All implants were placed in a mid-sagittal, median or paramedian palatal location by the same surgeon. They were orthodontically loaded after a healing period of 8-16 weeks (Mean: 12.8 weeks). RESULTS AND DISCUSSION: Of the initially 70 consecutively admitted patients, two implants in two patients were not primary stable after installation and had to be removed. Of the 70 initially installed palatal implants, 67 implants or 95.7% osseointegrated successfully and were loaded actively and/or passively for approximately 19 months. Only one implant of the 67 osseointegrated implants lost its stability under orthodontic loading. By the time of re-evaluation, 20 palatal implants were still used for orthodontic therapy, while 46 implants had been removed after completed orthodontic therapy. By only analyzing those, the success rate of the initially installed implants was 92%. CONCLUSIONS: Orthodontic palatal implants with a rough surface are predictable and highly reliable devices for a multitude of maxillary orthodontic treatment options. The survival and success rates for palatal orthodontic implants are comparable to dental implants installed for dental prostheses

Soft tissue stability after segmental distraction of the anterior mandibular alveolar process: a 5.5 year follow-up

Item does not contain fulltextSoft tissue changes were analysed retrospectively in 17 patients following distraction osteogenesis (DO) of the mandibular anterior alveolar process. Lateral cephalograms were traced by hand, digitized, superimposed, and evaluated at T1 (17.0 days), after DO at T2 (mean 6.5 days), at T3 (mean 24.4 days), at T4 (mean 2.0 years), and at T5 (mean 5.5 years). Statistical analysis was carried out using Kolmogorov-Smirnov test, paired t-test, Pearson's correlation coefficient, and linear backward regression analysis. 5.5 years postoperatively, the net effect for the soft tissue at point B' was 88% of the advancement at point B while the lower lip (labrale inferior) followed the advancement of incision inferior to 24%. Increased preoperative age was correlated (p<0.05) with more horizontal backward movement (T5-T3) for labrale inferior and pogonion'. Higher NL/ML' angles were significantly correlated (p<0.05) to smaller horizontal soft tissue change at labrale inferior (T5-T3). The amount of advancement at point B was significantly correlated with an upward movement (T5-T3) of labrale inferior (p<0.01) and stomion inferior (p<0.05). It can be concluded that further change in soft tissues occurred between 2.0 and 5.5 years postoperatively. The physiological process of ageing and loss of soft tissue elasticity should be considered as possible reasons