Electric Field Analysis of Breast Tumor Cells

An attractive alternative treatment for malignant tumors that are refractive to conventional therapies, such as surgery, radiation, and chemotherapy, is electrical-pulse-mediated drug delivery. Electric field distribution of tissue/tumor is important for effective treatment of tissues. This paper deals with the electric field distribution study of a tissue model using MAXWELL 3D Simulator. Our results indicate that tumor tissue had lower electric field strength compared to normal cells, which makes them susceptible to electrical-pulse-mediated drug delivery. This difference could be due to the altered properties of tumor cells compared to normal cells, and our results corroborate this

Tomorrow's Surgery: Micromotors and Microrobots

Surgical procedures have changed radically over the last few years due to the arrival of new technology. What will technology bring us in the future? This paper examines a few of the forces whose timing are causing new ideas to congeal from the fields of artificial intelligence, robotics, micromachining and smart materials. Intelligence systems for autonomous mobile robots can now enable simple insect level behaviors in small amounts of silicon. These software breakthroughs coupled with new techniques for microfabricating miniature sensors and actuators from both silicon and ferroelectric families of materials offer glimpses of the future where robots will be small, cheap and potentially useful to surgeons. In this paper we relate our recent efforts to fabricate piezoelectric micromotors in an effort to develop actuator technologies where brawn matches to the scale of the brain. We discuss our experiments with thin film ferroelectric motors 2mm in diameter and larger 8mm versions machined from bulk ceramic and sketch possible applications in the surgical field.MIT Artificial Intelligence Laborator

Report on swimbladder disorder in the honeycomb grouper, Epinephelus merra

Swimbladder or airbladder is a thin layered epithelial sac filled with air, lying above the alimentary canal of bony fishes that regulates buoyancy of the fish so that the specific gravity of the fish always matches the depth at which it is swimming. Swimbladder disorder (SBD) is a condition caused by sudden temperature changes impacted stomach resulting from improper feeding or due to bacterial or viral infections of the bladder characterised by inability of the fish to keep a normal upright position in water. Normally gold fishes suffer from SBD due to their globoid body shape. Fish with SBD may float on their side or their back, swim in circles or take head-down posture

STIFDB—Arabidopsis Stress Responsive Transcription Factor DataBase

Elucidating the key players of molecular mechanism that mediate the complex stress-responses in plants system is an important step to develop improved variety of stress tolerant crops. Understanding the effects of different types of biotic and abiotic stress is a rapidly emerging domain in the area of plant research to develop better, stress tolerant plants. Information about the transcription factors, transcription factor binding sites, function annotation of proteins coded by genes expressed during abiotic stress (for example: drought, cold, salinity, excess light, abscisic acid, and oxidative stress) response will provide better understanding of this phenomenon. STIFDB is a database of abiotic stress responsive genes and their predicted abiotic transcription factor binding sites in Arabidopsis thaliana. We integrated 2269 genes upregulated in different stress related microarray experiments and surveyed their 1000 bp and 100 bp upstream regions and 5′UTR regions using the STIF algorithm and identified putative abiotic stress responsive transcription factor binding sites, which are compiled in the STIFDB database. STIFDB provides extensive information about various stress responsive genes and stress inducible transcription factors of Arabidopsis thaliana. STIFDB will be a useful resource for researchers to understand the abiotic stress regulome and transcriptome of this important model plant system

A Sustainable Technique for Colony Multiplication by Eduction of Wild Nests of the Stingless Bee Tetragonula iridipennis Smith

Colony multiplication of stingless bees, Tetragonula iridipennis, largely relies on the eduction of wild colonies from their natural nesting sites in India. During the hiving of wild colonies, colonies were destroyed with the loss of robust wild foragers and built-in storage reserves over the years. The present study was conducted to devise a technique to sustainably multiply the colonies of stingless bees from the wild colony and the colony establishment and development during the eduction process. The annexure hives provided for eduction were accepted in a shorter time (3.25 ± 1.18 days), with the construction of storage pots observed at 7.75 ± 1.59 days after hive acceptance by the bees. The movement of foragers between the wild colony and the annexure hives was noticed for 13.80 ± 4.20 days. The foragers settled in the annexure hives and started foraging after 18.20 ± 2.49 days. The advancing fronts were observed at 26.67 ± 2.58 days after the addition of the laying queen in the established annexure hives. There was a significant increase in the number of inhive workers after the queen seeding in the annexure hives. This technique is the easiest and most sustainable non- destructive way of multiplication of stingless bee colonies without loss in viability of the perennial wild colony

Combined use of expression and CGH arrays pinpoints novel candidate genes in Ewing sarcoma family of tumors

<p>Abstract</p> <p>Background</p> <p>Ewing sarcoma family of tumors (ESFT), characterized by t(11;22)(q24;q12), is one of the most common tumors of bone in children and young adults. In addition to <it>EWS/FLI1 </it>gene fusion, copy number changes are known to be significant for the underlying neoplastic development of ESFT and for patient outcome. Our genome-wide high-resolution analysis aspired to pinpoint genomic regions of highest interest and possible target genes in these areas.</p> <p>Methods</p> <p>Array comparative genomic hybridization (CGH) and expression arrays were used to screen for copy number alterations and expression changes in ESFT patient samples. A total of 31 ESFT samples were analyzed by aCGH and in 16 patients DNA and RNA level data, created by expression arrays, was integrated. Time of the follow-up of these patients was 5–192 months. Clinical outcome was statistically evaluated by Kaplan-Meier/Logrank methods and RT-PCR was applied on 42 patient samples to study the gene of the highest interest.</p> <p>Results</p> <p>Copy number changes were detected in 87% of the cases. The most recurrent copy number changes were gains at 1q, 2, 8, and 12, and losses at 9p and 16q. Cumulative event free survival (ESFT) and overall survival (OS) were significantly better (P < 0.05) for primary tumors with three or less copy number changes than for tumors with higher number of copy number aberrations. In three samples copy number imbalances were detected in chromosomes 11 and 22 affecting the <it>FLI1 </it>and <it>EWSR1 </it>loci, suggesting that an unbalanced t(11;22) and subsequent duplication of the derivative chromosome harboring fusion gene is a common event in ESFT. Further, amplifications on chromosomes 20 and 22 seen in one patient sample suggest a novel translocation type between <it>EWSR1 </it>and an unidentified fusion partner at 20q. In total 20 novel ESFT associated putative oncogenes and tumor suppressor genes were found in the integration analysis of array CGH and expression data. Quantitative RT-PCR to study the expression levels of the most interesting gene, <it>HDGF</it>, confirmed that its expression was higher than in control samples. However, no association between <it>HDGF </it>expression and patient survival was observed.</p> <p>Conclusion</p> <p>We conclude that array CGH and integration analysis proved to be effective methods to identify chromosome regions and novel target genes involved in the tumorigenesis of ESFT.</p

Thrombosis in vasculitis: from pathogenesis to treatment

In recent years, the relationship between inflammation and thrombosis has been deeply investigated and it is now clear that immune and coagulation systems are functionally interconnected. Inflammation-induced thrombosis is by now considered a feature not only of autoimmune rheumatic diseases, but also of systemic vasculitides such as Behçet’s syndrome, ANCA-associated vasculitis or giant cells arteritis, especially during active disease. These findings have important consequences in terms of management and treatment. Indeed, Behçet’syndrome requires immunosuppressive agents for vascular involvement rather than anticoagulation or antiplatelet therapy, and it is conceivable that also in ANCA-associated vasculitis or large vessel-vasculitis an aggressive anti-inflammatory treatment during active disease could reduce the risk of thrombotic events in early stages. In this review we discuss thrombosis in vasculitides, especially in Behçet’s syndrome, ANCA-associated vasculitis and large-vessel vasculitis, and provide pathogenetic and clinical clues for the different specialists involved in the care of these patients