41 research outputs found
New Suggestions for the Mechanical Control of Bone Remodeling
Bone is constantly renewed over our lifetime through the process of bone (re)modeling. This process is important for bone to allow it to adapt to its mechanical environment and to repair damage from everyday life. Adaptation is thought to occur through the mechanosensitive response controlling the bone-forming and -resorbing cells. This report shows a way to extract quantitative information about the way remodeling is controlled using computer simulations. Bone resorption and deposition are described as two separate stochastic processes, during which a discrete bone packet is removed or deposited from the bone surface. The responses of the bone-forming and -resorbing cells to local mechanical stimuli are described by phenomenological remodeling rules. Our strategy was to test different remodeling rules and to evaluate the time evolution of the trabecular architecture in comparison to what is known from μ-CT measurements of real bone. In particular, we tested the reaction of virtual bone to standard therapeutic strategies for the prevention of bone deterioration, i.e., physical activity and medications to reduce bone resorption. Insensitivity of the bone volume fraction to reductions in bone resorption was observed in the simulations only for a remodeling rule including an activation barrier for the mechanical stimulus above which bone deposition is switched on. This is in disagreement with the commonly used rules having a so-called lazy zone
Nuclear localisation of Aurora-A: its regulation and significance for Aurora-A functions in cancer.
The Aurora-A kinase regulates cell division, by controlling centrosome biology and spindle assembly. Cancer cells often display elevated levels of the kinase, due to amplification of the gene locus, increased transcription or post-translational modifications. Several inhibitors of Aurora-A activity have been developed as anti-cancer agents and are under evaluation in clinical trials. Although the well-known mitotic roles of Aurora-A point at chromosomal instability, a hallmark of cancer, as a major link between Aurora-A overexpression and disease, recent evidence highlights the existence of non-mitotic functions of potential relevance. Here we focus on a nuclear-localised fraction of Aurora-A with oncogenic roles. Interestingly, this pool would identify not only non-mitotic, but also kinase-independent functions of the kinase. We review existing data in the literature and databases, examining potential links between Aurora-A stabilisation and localisation, and discuss them in the perspective of a more effective targeting of Aurora-A in cancer therapy
Chickpea
The narrow genetic base of cultivated chickpea warrants systematic collection,
documentation and evaluation of chickpea germplasm and particularly wild
Cicer species for effective and efficient use in chickpea breeding programmes.
Limiting factors to crop production, possible solutions and ways to overcome
them, importance of wild relatives and barriers to alien gene introgression and
strategies to overcome them and traits for base broadening have been discussed.
It has been clearly demonstrated that resistance to major biotic and abiotic
stresses can be successfully introgressed from the primary gene pool
comprising progenitor species. However, many desirable traits including high
degree of resistance to multiple stresses that are present in the species
belonging to secondary and tertiary gene pools can also be introgressed by
using special techniques to overcome pre- and post-fertilization barriers.
Besides resistance to various biotic and abiotic stresses, the yield QTLs have
also been introgressed from wild Cicer species to cultivated varieties. Status
and importance of molecular markers, genome mapping and genomic tools
for chickpea improvement are elaborated. Because of major genes for various
biotic and abiotic stresses, the transfer of agronomically important traits into
elite cultivars has been made easy and practical through marker-assisted
selection and marker-assisted backcross. The usefulness of molecular markers
such as SSR and SNP for the construction of high-density genetic maps of
chickpea and for the identification of genes/QTLs for stress resistance, quality
and yield contributing traits has also been discussed
Plane Wave Diffraction by Dielectric Loaded Thick-walled Parallel-plate Impedance Waveguide - Abstract
Development of an intravaginal ring for the topical delivery of Aurora kinase A inhibitor, MLN8237.
Human papilloma virus (HPV) is the main culprit in cervical cancers. Although the HPV vaccine is now available, the slow and gradual process for HPV cancers to form means little will change, even for vaccinated individuals. This warrants the development of new therapeutic strategies in both the newly diagnosed and recurrent patients. We have previously shown that Alisertib (MLN8237), an Aurora A kinase inhibitor, potently and selectively kills HPV-positive cervical cancer cells. However, Alisertib is known for its unfavorable side effects when administered systemically. A targeted delivery approach is therefore warranted. The topical delivery of drugs to the cervix for the treatment of cervical cancer is an underexplored area of research that has the potential to significantly improve therapeutic outcome. Here, we design a novel topical drug delivery system for localized delivery in the vaginal tract using intravaginal silicone rings loaded with Alisertib. We assessed the suitability of the drug for the application and delivery method and develop a high-performance liquid chromatography method, then show that the vaginal rings were effective at releasing Alisertib over an extended period of time. Furthermore, we showed that Alisertib-loaded vaginal rings did not induce overt inflammation in the mouse vaginal tract. Our work has major translational implications for the future development of vaginal ring devices for the topical treatment of cervical cancer
Optimal Sensor Deployment According to a New Approach for Target Tracking in Smart Homes
International audienc
T-786 C POLYMORPHISM OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE GENE IS ASSOCIATED WITH CORONARY ARTERY DISEASE
WOS: 000317946500302