Immunohistochemical expression of hyaluronic acid in the normal prostate, benign prostate hyperplasia and prostate carcinoma

Hyaluronic acid (HA), a component of the extracellular matrix, is present in various tissues and tissue fluids. HA regulates cell adhesion and migration and it has been implicated in the progression of prostate cancer (PCa) as a molecule associated with the biological potential of PCa. The concentration of HA is elevated in several cancers, including bladder, colon, breast and Wilms’ tumor. In this study, we compared the immunohistochemical expression of HA in the normal prostate, benign prostate hyperplasia (BPH) and prostate carcinoma. HA was immunohistochemically detected in 22 prostate tissues (6 histologically normal, 10 with BPH and 6 with PCa). Formalin fixed, paraffin-embedded sections were stained using an ABC method with biotinylated HA binding protein (B-HABP). Negative controls included sections incubated without B-HABP as well as sections incubated with Streptomyces hyaluronidase. In normal and BPH prostate glands staining was localized predominantly in the gland surrounding stroma, as well as in the fibrovascular core of the papillary projections of the glands. In prostate carcinoma samples the amount of HA in the stroma was markedly increased and staining was not localized around glandular structures but was diffuse throughout the stroma. There was a sharp diminution at the interface between tumor stroma and non-tumoral connective tissue. HA appears to be a supplementary tumor-associated marker. Insight gained in the mechanisms of increased production and hyaluronidase digestion of HA may eventually lead to new targets for pharmacological intervention in the treatment of PCa

Fire Retardant Action of Layered Double Hydroxides and Zirconium Phosphate Nanocomposites Fillers in Polyisocyanurate Foams

Modern day energy codes are driving the design and multi-layered configuration of exterior wall systems with a significant emphasis on achieving high performance insulation towards improving energy performance of building envelopes. Use of highly insulating polyisocyanurate (PIR) based materials enhanced with eco-friendly lamellar inorganic fillers reinforces energy performance requirements, environmental challenges and cost reduction without compromising the overall building fire safety. The current work assessed the fire behaviour of PIR modified with three layered fillers, namely MgAlCO3 (PIR-LDH1), MgAl Stearate (PIR-LDH2) and Zirconium Phosphate octadecylamine (PIR-ZrP3). For each of the fillers, three loadings (2, 4 and 6% by weight) were used. Optical analysis by X-ray diffraction patterns (XRD), cone calorimeter (CC), thermogravimetric (TGA) analysis, post-burning morphological evaluation using field emission scanning electron microscope (FESEM) and diffuse reflectance infrared spectroscopy (DRIFT) analysis, were performed. The results indicated that fire reaction properties and thermal stability of foam samples were enhanced with all three different lamellar inorganic smart fillers. The initial degradation temperature of PIR-layered filler samples was increased, demonstrating that incorporation of flame retardants decelerated the degradation of the PIR foam and contributed to significant char formation, from 19.5% in pure PIR samples to 33% in PIR-6%LDH1 samples. Increasing the filler content also resulted in improved char properties and decreased peak Heat Release Rates (HRR) in the cone calorimeter. Due to the development of a stable char layer, samples containing 6% of ZrP3 did not ignite at 20 kW/m2 and a reduction of up to 40% in the peak HRR was achieved in PIR-2%ZrP3 samples

Critical aspects of three-dimensional anisotropic spin-glass models

We study the $\pm J$ three-dimensional Ising model with a longitudinal anisotropic bond randomness on the simple cubic lattice. The random exchange interaction is applied only in the $z$ direction, whereas in the other two directions, $xy$ - planes, we consider ferromagnetic exchange. By implementing an effective parallel tempering scheme, we outline the phase diagram of the model and compare it to the corresponding isotropic one, as well as to a previously studied anisotropic (transverse) case. We present a detailed finite-size scaling analysis of the ferromagnetic - paramagnetic and spin glass - paramagnetic transition lines, and we also discuss the ferromagnetic - spin glass transition regime. We conclude that the present model shares the same universality classes with the isotropic model, but at the symmetric point has a considerably higher transition temperature from the spin-glass state to the paramagnetic phase. Our data for the ferromagnetic - spin glass transition line are supporting a forward behavior in contrast to the reentrant behavior of the isotropic model.Comment: 10 pages, 9 eps figures, 1 table, corrected symbolis

Mediastinitis complicating a percutaneous endoscopic gastrostomy: a case report

BACKGROUND: Since its introduction in the early 1980s, percutaneous endoscopic gastrostomy has become the most popular method for performing a gastrostomy for long-term enteral feeding. It has been associated, however, with a lot of minor and major complications. CASE PRESENTATION: A case of mediastinitis with concominant sepsis caused by a masked esophageal perforation after percutaneous endoscopic gastrostomy in a multi-traumatized, brain-injured patient is presented. Ten – fourteen days after the procedure, the patient became febrile and gradually septic with tenderness of the sternum and upper abdomen. Computerized tomography of the thorax revealed mediastinitis. An urgent left thoracotomy and laparotomy were performed for drainage of the mediastinum, removal of the gastrostomy and insertion of a jejunostomy tube. The patient improved soon after the surgery. He was successfully weaned off the ventilator and was discharged from the Intensive Care Unit. CONCLUSION: Perforating mediastinitis is a rare but potentially lethal complication of percutaneous endoscopic gastrostomy. When diagnosed and properly treated it may have a favourable outcome

The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.

Rare disease patients are more likely to receive a rapid molecular diagnosis nowadays thanks to the wide adoption of next-generation sequencing. However, many cases remain undiagnosed even after exome or genome analysis, because the methods used missed the molecular cause in a known gene, or a novel causative gene could not be identified and/or confirmed. To address these challenges, the RD-Connect Genome-Phenome Analysis Platform (GPAP) facilitates the collation, discovery, sharing, and analysis of standardized genome-phenome data within a collaborative environment. Authorized clinicians and researchers submit pseudonymised phenotypic profiles encoded using the Human Phenotype Ontology, and raw genomic data which is processed through a standardized pipeline. After an optional embargo period, the data are shared with other platform users, with the objective that similar cases in the system and queries from peers may help diagnose the case. Additionally, the platform enables bidirectional discovery of similar cases in other databases from the Matchmaker Exchange network. To facilitate genome-phenome analysis and interpretation by clinical researchers, the RD-Connect GPAP provides a powerful user-friendly interface and leverages tens of information sources. As a result, the resource has already helped diagnose hundreds of rare disease patients and discover new disease causing genes