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1.
Oncogene ; 32(34): 3923-32, 2013 Aug 22.
Artigo em Inglês | MEDLINE | ID: mdl-23246968

RESUMO

The target of rapamycin (TOR) pathway is highly conserved among eukaryotes and has evolved to couple nutrient sensing to cellular growth. TOR is found in two distinct signaling complexes in cells, TOR complex 1 (TORC1) and TOR complex 2 (TORC2). These complexes are differentially regulated and act as effectors for the generation of signals that drive diverse cellular processes such as growth, proliferation, protein synthesis, rearrangement of the cytoskeleton, autophagy, metabolism and survival. Mammalian TOR (mTOR) is very important for development in embryos, while in adult organisms it is linked to aging and lifespan effects. In humans, the mTOR pathway is implicated in the tumorigenesis of multiple cancer types and its deregulation is associated with familial cancer syndromes. Because of its high biological relevance, different therapeutic strategies have been developed to target this signaling cascade, resulting in the emergence of unique pharmacological inhibitors that are either already approved for use in clinical oncology or currently under preclinical or clinical development. Multimodal treatment strategies that simultaneously target multiple nodes of the pathway and/or negative feedback regulatory loops may ultimately provide the best therapeutic advantage in targeting this pathway for the treatment of malignancies.


Assuntos
Evolução Molecular , Neoplasias/genética , Transdução de Sinais/genética , Serina-Treonina Quinases TOR/genética , Animais , Antineoplásicos/uso terapêutico , Fenômenos Fisiológicos Celulares/efeitos dos fármacos , Fenômenos Fisiológicos Celulares/genética , Fenômenos Fisiológicos Celulares/fisiologia , Regulação da Expressão Gênica/efeitos dos fármacos , Humanos , Modelos Genéticos , Neoplasias/tratamento farmacológico , Neoplasias/metabolismo , Transdução de Sinais/efeitos dos fármacos , Transdução de Sinais/fisiologia , Serina-Treonina Quinases TOR/antagonistas & inibidores , Serina-Treonina Quinases TOR/metabolismo
2.
Phys Rev Lett ; 109(3): 032505, 2012 Jul 20.
Artigo em Inglês | MEDLINE | ID: mdl-22861843

RESUMO

We report on a search for neutrinoless double-beta decay of 136Xe with EXO-200. No signal is observed for an exposure of 32.5 kg yr, with a background of ∼1.5×10(-3) kg(-1) yr(-1) keV(-1) in the ±1σ region of interest. This sets a lower limit on the half-life of the neutrinoless double-beta decay T(1/2)(0νßß)(136Xe)>1.6×10(25) yr (90% C.L.), corresponding to effective Majorana masses of less than 140-380 meV, depending on the matrix element calculation.

3.
Oncogene ; 31(3): 269-81, 2012 Jan 19.
Artigo em Inglês | MEDLINE | ID: mdl-21706056

RESUMO

Ezrin is a multifunctional protein that connects the actin cytoskeleton to the extracellular matrix through transmembrane proteins. High ezrin expression is associated with lung metastasis and poor survival in cancer. We screened small molecule libraries for compounds that directly interact with ezrin protein using surface plasmon resonance to identify lead compounds. The secondary functional assays used for lead compound selection included ezrin phosphorylation as measured by immunoprecipitation and in vitro kinase assays, actin binding, chemotaxis, invasion into an endothelial cell monolayer, zebrafish and Xenopus embryonic development, mouse lung organ culture and an in vivo lung metastasis model. Two molecules, NSC305787 and NSC668394, that directly bind to ezrin with low micromolar affinity were selected based on inhibition of ezrin function in multiple assays. They inhibited ezrin phosphorylation, ezrin-actin interaction and ezrin-mediated motility of osteosarcoma (OS) cells in culture. NSC305787 mimicked the ezrin morpholino phenotype, and NSC668394 caused a unique developmental defect consistent with reduced cell motility in zebrafish. Following tail vein injection of OS cells into mice, both molecules inhibited lung metastasis of ezrin-sensitive cells, but not ezrin-resistant cells. The small molecule inhibitors NSC305787 and NSC668394 demonstrate a novel targeted therapy that directly inhibits ezrin protein as an approach to prevent tumor metastasis.


Assuntos
Adamantano/análogos & derivados , Antineoplásicos/farmacologia , Neoplasias Ósseas/patologia , Proteínas do Citoesqueleto/antagonistas & inibidores , Neoplasias Pulmonares/secundário , Osteossarcoma/secundário , Fenóis/farmacologia , Quinolinas/farmacologia , Quinolonas/farmacologia , Actinas/antagonistas & inibidores , Adamantano/química , Adamantano/farmacologia , Animais , Antineoplásicos/química , Linhagem Celular Tumoral , Movimento Celular/efeitos dos fármacos , Feminino , Camundongos , Camundongos Endogâmicos BALB C , Invasividade Neoplásica/patologia , Técnicas de Cultura de Órgãos , Osteossarcoma/metabolismo , Fenóis/química , Fosforilação/efeitos dos fármacos , Quinolinas/química , Quinolonas/química , Ressonância de Plasmônio de Superfície , Xenopus , Peixe-Zebra
4.
Phys Rev Lett ; 107(21): 212501, 2011 Nov 18.
Artigo em Inglês | MEDLINE | ID: mdl-22181874

RESUMO

We report the observation of two-neutrino double-beta decay in (136)Xe with T(1/2) = 2.11 ± 0.04(stat) ± 0.21(syst) × 10(21) yr. This second-order process, predicted by the standard model, has been observed for several nuclei but not for (136)Xe. The observed decay rate provides new input to matrix element calculations and to the search for the more interesting neutrinoless double-beta decay, the most sensitive probe for the existence of Majorana particles and the measurement of the neutrino mass scale.

5.
Animal ; 2(4): 636-44, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-22443581

RESUMO

Various strategies have been developed to increase the cellular level of (n-3) polyunsaturated fatty acids in animals and humans. In the present study, we investigated the effect of dietary myristic acid, which represents 9% to 12% of fatty acids in milk fat, on the storage of α-linolenic acid and its conversion to highly unsaturated (n-3) fatty acid derivatives. Five isocaloric diets were designed, containing equal amounts of α-linolenic acid (1.3% of dietary fatty acids, i.e. 0.3% of dietary energy) and linoleic acid (7.0% of fatty acids, i.e. 1.5% of energy). Myristic acid was supplied from traces to high levels (0%, 5%, 10%, 20% and 30% of fatty acids, i.e. 0% to 6.6% of energy). To keep the intake of total fat and other saturated fatty acids constant, substitution was made with decreasing levels of oleic acid (76.1% to 35.5% of fatty acids, i.e. 16.7% to 7.8% of energy) that is considered to be neutral in lipid metabolism. After 8 weeks, results on physiological parameters showed that total cholesterol and low-density lipoprotein-cholesterol did not differ in the diets containing 0%, 5% and 10% myristic acid, but were significantly higher in the diet containing 30% myristic acid. In all the tissues, a significant increasing effect of the substitution of oleic acid for myristic acid was shown on the level of both α-linolenic and linoleic acids. Compared with the rats fed the diet containing no myristic acid, docosahexaenoic acid significantly increased in the brain and red blood cells of the rats fed the diet with 30% myristic acid and in the plasma of the rats fed the diet with 20% myristic acid. Arachidonic acid also increased in the brain of the rats fed the diet with 30% myristic acid. By measuring Δ6-desaturase activity, we found a significant increase in the liver of the rats fed the diet containing 10% of myristic acid but no effect at higher levels of myristic acid. These results suggest that an increase in dietary myristic acid may contribute in increasing significantly the tissue storage of α-linolenic acid and the overall bioavailability of (n-3) polyunsaturated fatty acids in the brain, red blood cells and plasma, and that mechanisms other than the single Δ6-desaturase activity are involved in this effect.

6.
Appl Environ Microbiol ; 49(1): 217-20, 1985 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16346699

RESUMO

The alleviation of the acetylene blockage of nitrous oxide reduction by sulfide was studied in anaerobically incubated Brookston soil to better characterize the process. Removal of nitrate-derived nitrous oxide from soil amended with acetylene and sulfide occurred earlier in the presence of glucose than it did in its absence. This was attributed to the influence of glucose on nitrous oxide production rather than reduction during the early stages of the soil incubation. Glucose was found to have no effect on reduction of injected nitrous oxide in the presence of acetylene- and sulfide-amended soil, whereas carbon dioxide significantly stimulated reduction. It is suggested that the microorganism(s) involved may use carbon dioxide as a cellular carbon source. The sulfide added to the soil probably did not act solely as an electron donor, as the number of electrons required to reduce the added nitrous oxide in our systems was greater than the amount supplied by the sulfide. The soil pH at which the alleviation occurred was 6.7 and was not affected by the sulfide treatment.

7.
J Environ Sci Health B ; 14(5): 459-74, 1979.
Artigo em Inglês | MEDLINE | ID: mdl-38271

RESUMO

The disposal of digested sewage sludge on crop-producing land appeals to municipalities as an option but may pose a hazard to human and animal health if the plant material contains elevated levels of some heavy metals. This paper reports the levels of cadmium in corn grain and stover for six years -- three years with sludge applied annually and for three years after sludge applications were terminated. The cadmium concentration in corn grain from the sixth year was similar to values found in corn grown on non-sludged plots. In corn stover from treated plots the cadmium concentration was greater than from untreated plots. Our study indicated that phytotoxic levels of cadmium did not exist even though elevated levels occurred in the corn stover.


Assuntos
Cádmio/análise , Esgotos/análise , Poluentes do Solo/análise , Zea mays/análise , Cobre/análise , Concentração de Íons de Hidrogênio , Chumbo/análise , Manganês/análise , Níquel/análise , Plantas/análise , Fatores de Tempo , Zinco/análise
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