Clinical, radiological and therapeutic features of keratocystic odontogenic tumours: a study over a decade

Factors associated with the potential for recurrence of keratocystic odontogenic tumours (KCOT) still remain to be clearly determined and no consensus exists concerning the management of KCOT. The purpose of this study was to evaluate different clinical factors associated with KCOT and its treatment methods. A retrospective review was performed of 55 cases treated from 2001 to 2010. Of the 55 cases, 27% were associated with an impacted or semi- impacted tooth. The majority of the lesions (82%) were located in tooth-bearing areas, and the overall mandibular to maxilla ratio of tumour occurrence was 5:1. The treatment options included enucleation, marsupialisation, or peripheral ostectomy, with or without the use of Carnoy ?s solution. Recurrence was found in 14 cases (25%). No significant association was seen between recurrence and age, symptomatic cases, location of the lesion, or unilocu - lar or multilocular appearance. The recurrence rate was higher in the group with tooth involvement, more marked in cases with third molar involvement. Statistical analysis showed a significant relation between recurrence and the type of treatment, with higher rates in cases treated with enucleation associated with tooth extraction. In our series, those cases with a closer relation with dental tissues showed a higher risk of recurrence, suggesting the need for a distinct classification for peripheral variants of KCOT

On the Controllability of Parabolic Systems with a Nonlinear Term Involving the State and the Gradient

We present some results concerning the controllability of a quasi-linear parabolic equation (with linear principal part) in a bounded domain of ${\mathbb R}^N$ with Dirichlet boundary conditions. We analyze the controllability problem with distributed controls (supported on a small open subset) and boundary controls (supported on a small part of the boundary). We prove that the system is null and approximately controllable at any time if the nonlinear term $f( y, \nabla y)$ grows slower than $|y| \log^{3/2}(1+ |y| + |\nabla y|) + |\nabla y| \log^{1/2}(1+ |y| + |\nabla y|)$ at infinity (generally, in this case, in the absence of control, blow-up occurs). The proofs use global Carleman estimates, parabolic regularity, and the fixed point method

The Proteasomal Deubiquitinating Enzyme PSMD14 Regulates Macroautophagy by Controlling Golgi-to-ER Retrograde Transport

Ubiquitination regulates several biological processes, however the role of specific members of the ubiquitinome on intracellular membrane trafficking is not yet fully understood. Here, we search for ubiquitin-related genes implicated in protein membrane trafficking performing a High-Content siRNA Screening including 1187 genes of the human “ubiquitinome” using amyloid precursor protein (APP) as a reporter. We identified the deubiquitinating enzyme PSMD14, a subunit of the 19S regulatory particle of the proteasome, specific for K63-Ub chains in cells, as a novel regulator of Golgi-to-endoplasmic reticulum (ER) retrograde transport. Silencing or pharmacological inhibition of PSMD14 with Capzimin (CZM) caused a robust increase in APP levels at the Golgi apparatus and the swelling of this organelle. We showed that this phenotype is the result of rapid inhibition of Golgi-to-ER retrograde transport, a pathway implicated in the early steps of the autophagosomal formation. Indeed, we observed that inhibition of PSMD14 with CZM acts as a potent blocker of macroautophagy by a mechanism related to the retention of Atg9A and Rab1A at the Golgi apparatus. As pharmacological inhibition of the proteolytic core of the 20S proteasome did not recapitulate these effects, we concluded that PSMD14, and the K63-Ub chains, act as a crucial regulatory factor for macroautophagy by controlling Golgi-to-ER retrograde transport

Use of simple noninvasive biomarkers to predict liver fibrosis in HIV/HCV coinfection in routine clinical practice

This study was supported by a grant from Abbott Laboratories. The authors wish to thank the Spanish Health Ministry (ISCIII-RETIC RD06/006) for financial support.Background Simple noninvasive tests to predict fibrosis, as an alternative to liver biopsy (LB), are needed. Of these, the aspartate aminotransferase (AST) to platelet ratio index (APRI) and the Forns index (FI) have been validated in HIV/hepatitis C virus (HCV) coinfection. However, these indexes may have lower diagnostic value in situations other than the circumscribed conditions of validation studies. We therefore examined the value of the APRI and FI in HIV/HCV-coinfected patients for the detection of significant fibrosis in real-life conditions. Patients and methods HIV/HCV-coinfected patients who had participated in a multicentre cross-sectional retrospective study were selected if they had undergone an LB within 24 months before the last visit. The predictive accuracy of the APRI and FI was measured using the areas under receiver-operating-characteristic curves (AUROCs). Diagnostic accuracy was determined using the positive (PPV) and negative (NPV) predictive values. Results A total of 519 coinfected individuals were included in the study. The AUROC [95% confidence interval (95% CI)] of the APRI was 0.67 (0.66–0.71) and that of the FI was 0.67 (0.62–0.71). The PPV of the APRI was 79% and its NPV was 66%. The PPV of the FI was 74% and its NPV was 64%. LB length was available and was ≥15 mm in 120 individuals. In this group, the PPV of the APRI was 85%, and that of the FI was 81%. Using these indexes, 22% of patients could be spared LB. Applying both models sequentially, 30% of patients could be spared LB. Conclusions In HIV/HCV-coinfected patients, the diagnostic accuracy of the APRI in real-life conditions was similar to that in the validation studies. The FI performed less well. However, combining the two indexes to make decisions on anti-HCV therapy may prevent a significant proportion of patients from having to undergo LB.Abbott LaboratoriesSpanish Health Ministry (ISCIII-RETIC RD06/006

Mimicking bone microenvironment : 2D and 3D in vitro models of human osteoblasts

Understanding the in vitro biology and behavior of human osteoblasts is crucial for developing research models that reproduce closely the bone structure, its functions, and the cell-cell and cell-matrix interactions that occurs in vivo. Mimicking bone microenvironment is challenging, but necessary, to ensure the clinical translation of novel medicines to treat more reliable different bone pathologies. Currently, bone tissue engineering is moving from 2D cell culture models such as traditional culture, sandwich culture, micro-patterning, and altered substrate stiffness, towards more complex 3D models including spheroids, scaffolds, cell sheets, hydrogels, bioreactors, and microfluidics chips. There are many different factors, such cell line type, cell culture media, substrate roughness and stiffness that need consideration when developing in vitro models as they affect significantly the microenvironment and hence, the final outcome of the in vitro assay. Advanced technologies, such as 3D bioprinting and microfluidics, have allowed the development of more complex structures, bridging the gap between in vitro and in vivo models. In this review, past and current 2D and 3D in vitro models for human osteoblasts will be described in detail, highlighting the culture conditions and outcomes achieved, as well as the challenges and limitations of each model, offering a widen perspective on how these models can closely mimic the bone microenvironment and for which applications have shown more successful results

Autophagosomes cooperate in the degradation of intracellular C-terminal fragments of the amyloid precursor protein <i>via </i>the MVB/lysosomal pathway

© FASEB. Brain regions affected by Alzheimer disease (AD) displaywell-recognized early neuropathologic features in the endolysosomal and autophagy systems of neurons, including enlargement of endosomal compartments, progressive accumulation of autophagic vacuoles, and lysosomal dysfunction.Although the primary causes of these disturbances are still under investigation, a growing body of evidence suggests that the amyloid precursor protein (APP) intracellular C-terminal fragment b (C99), generated by cleavage of APP by b-site APP cleaving enzyme 1 (BACE-1), is the primary cause of the endosome enlargement inADand the earliest initiator of synaptic plasticity and long-termmemory impairment. The aimof the present study was to evaluate the possible relationship between the endolysosomal degradation pathway and autophagy on the proteolytic processing and turnover of C99. We found that pharmacologic treatments that either inhibit autophagosomeformationorblock the fusionof autophagosomes to

TELMA: Entorno de formación personalizada online en Cirugía de Mínima Invasión

TELMA es un entorno de formación y aprendizaje online basado en edición de vídeo laparoscópico, la gestión del conocimiento y el trabajo colaborativo con el fin de mejorar la efectividad y eficacia de los procesos de formación (inicial y continuada) de los cirujanos de Cirugía de Mínima Invasión (CMI). TELMA explota el uso del vídeo laparoscópico como el núcleo de los contenidos didácticos y hace uso de tecnologías de formación online y gestión de contenidos digitales multimedia, para mejorar la adaptación, calidad y eficiencia del servicio ofrecido al usuario. TELMA persigue acortar las curvas de aprendizaje, proporcionando a los cirujanos un acceso ubicuo a contenidos educativos y metodologías didácticas, dotando al aprendizaje de mayor interactividad y proporcionando a los alumnos un papel más activo, una mejor adquisición de los conocimientos y habilidades y un mayor uso de las fuentes de información disponibles

Papel de los factores bióticos y las sequías en el decaimiento del bosque: aportaciones desde la dendroecología

[ES] El aumento de la mortalidad y la pérdida de vitalidad de los bosques son procesos que afectan a diversas especies de árboles y biomas. Estos fenómenos de decaimiento forestal se han asociado a la interacción de múltiples factores relacionados con el cambio global, como el aumento de las sequías o la mayor incidencia de factores bióticos que generan estrés. Sin embargo, el papel que juegan estos organismos en el decaimiento del bosque en relación a la sequía no está del todo comprendido. En este trabajo caracterizamos retrospectivamente los efectos que ejercen dichos organismos sobre el crecimiento radial de árboles estresados por sequía utilizando dendrocronología. El efecto combinado del muérdago y las sequías reducen el crecimiento del pino silvestre y aumentan la defoliación, siendo estos efectos más evidentes en el ápice del árbol. La procesionaria induce pérdidas de crecimiento en pino laricio, pero en general se observa una recuperación dos años después. No encontramos un papel determinante de los hongos patógenos de raíz en el decaimiento del abeto. Finalmente, pinos carrasco muertos que presentaban ataques de insectos perforadores mostraron patrones de crecimiento similares a pinos vivos. Este estudio nos permite caracterizar algunos de los complejos y múltiples efectos de diferentes factores bióticos de estrés sobre el crecimiento y la vulnerabilidad de los bosques susceptibles a los efectos negativos de las sequías.[EN] Increasing mortality and decline of forests are affecting several tree species and biomes. These events of forest decline have been related to the interaction of several global change elements, like the increase in drought stress or a higher incidence of biotic stress factors. However, the roles played by biotic stressors have been scarcely explored as related to drought stress. In this paper we retrospectively characterize the effects of these organisms on radial growth of trees already stressed by drought using dendrochronology. The combined effect of mistletoe and droughts reduce tree growth in Scots pine and increase defoliation, being these effects more noticeable in the apex. The pine processionary moth induces growth losses in the affected stands of black pine, but they usually recover two years after the outbreak. We did not find a determinate role of root pathogens on silver fir dieback. Finally, dead Aleppo pine trees infested by bark beetles showed similar growth patterns than living pine trees. This study allows characterizing some of the complex and multiple effects of different biotic stressors on growth and vulnerability of forests subjected to the negative effects exerted by droughts.Este estudio ha sido financiado por los proyectos CGL2007- 66066-C04-02/BOS, CGL2008-04847-C02-01, CGL2011-26654 (MINECO), 387/2011 (Organismo Autónomo de Parques Nacionales) y PROCLIM (La Caixa-Gobierno de Aragón). Agradecemos la revisión realizada por dos revisores anónimos de una versión previa del texto. También queremos agradecer la ayuda prestada por todos los miembros del Laboratorio de Sanidad Forestal de Mora de Rubielos (Gobierno de Aragón), a todo el personal del Parque Nacional de Ordesa y Monte Perdido, al servicio de parques y jardines del Ayuntamiento de Zaragoza (Montserrat Hernández y José Bellosta), y a todos los APNs que nos han ayudado en las numerosas jornadas de campo. Finalmente, agradecemos a nuestros compañeros del IPE (CSIC) J.D. Galván y A.Q. Alla por su ayuda en los muestreos y la discusión de las ideas presentadas.Peer Reviewe

Evaluation of Clinical and Immunopathological Features of Different Infective Doses of Trypanosoma cruzi in Dogs during the Acute Phase

Infection with Trypanosoma cruzi is a major risk in Latin America, and dogs are believed to be good models for evaluating Chagas disease. Here, we evaluated the clinical and immunopathological alterations developed by mongrel dogs experimentally infected with different infective doses (2,000, 20,000, and 200,000 metacyclic trypomastigotes of Sylvio X10/4 strain kg−1 via intraperitoneal). Clinical and electrocardiographic parameters, as well as antibody production and pathologic lesions were evaluated. All three doses of this strain of T. cruzi induced a similar pattern of infection characterized by cardiac arrhythmias and severe and diffuse myocarditis. Specific anti-T. cruzi IgG indicated seroconversion by day 14 after infection, and IgG levels increased during the period of evaluation. Mortality was observed only in dogs infected with the medium or high parasite doses, but not in the group infected with a low dose of 2,000 parasites kg−1. Infection with a low dose of parasites provides an excellent nonlethal model to evaluate the immunopathology of the acute disease in dogs infected with the Sylvio X10/4 strain of T. cruzi

Synthesis, crystal structure and cytotoxicity assays of a copper(II) nitrate complex with a tridentate ONO acylhydrazone ligand. Spectroscopic and theoretical studies of the complex and its ligand

The new copper complex, [Cu(HL)(OH2)2](NO3), including the tridentate N-acyhydrazone derived from 4-hydroxy-benzohydrazide and 2-hydroxy-3-methoxybenzaldehyde, (H2L), has been synthesized and characterized in the solid state and in solution by spectroscopic (FTIR, Ra, UV–vis, EPR) methods. The results were compared with those obtained for the hydrazone ligand and complemented with computational methods based on DFT. The crystal structure of the complex has been determined by X-ray diffraction. It crystallizes in the triclinic space group with Z = 2. The Cu(II) ion is in a distorted square pyramidal environment, coordinated to a planar HL- anion acting as a tridentate ligand. The 5-fold coordination is completed with two water molecules. It is arranged in the lattice as H-bonded ribbon-like polymers that extends along the [1 2 1] crystal direction. The cytotoxicity of the complex together with that of the H2L ligand and the copper ion were evaluated in vitro against five different human cancer cell lines namely A549 (lung), MG-63 (bone), MCF-7 and MDA-MB-231 (breast) and Jurkat (leukemia). The copper complex inhibits the cell viability in a dose dependent manner with a greater potency than the H2L ligand and the free copper ion displaying even higher antitumor activity than the well-known anticancer metallodrug cisplatin.CONICET (PIP 11220130100651CO and PIP 0034), UNLP (111/X673) and ANPCyT (PICT 2014-2223) of Argentina. Consejería de Educación CyL and FFEDER BU076U16, BU022G18 and Ministerio de Economía y Competitividad CTQ2016-75023-C2-1-P and CTQ2015-70371-REDTMetDrugs Network (Spain