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1.
Mem. Inst. Oswaldo Cruz ; 108(2): 220-228, abr. 2013. tab, graf
Artigo em Inglês | LILACS | ID: lil-670400

RESUMO

To explore the effects of deforestation and resulting differences in vegetation and land cover on entomological parameters, such as anopheline species composition, abundance, biting rate, parity and entomological inoculation rate (EIR), three villages were selected in the Lower Caura River Basin, state of Bolívar, Venezuela. All-night mosquito collections were conducted between March 2008-January 2009 using CDC light traps and Mosquito Magnet(r) Liberty Plus. Human landing catches were performed between 06:00 pm-10:00 pm, when anophelines were most active. Four types of vegetation were identified. The Annual Parasite Index was not correlated with the type of vegetation. The least abundantly forested village had the highest anopheline abundance, biting rate and species diversity. Anopheles darlingi and Anopheles nuneztovari were the most abundant species and were collected in all three villages. Both species showed unique biting cycles. The more abundantly forested village of El Palmar reported the highest EIR. The results confirmed previous observations that the impacts of deforestation and resulting changes in vegetation cover on malaria transmission are complex and vary locally.


Assuntos
Animais , Feminino , Humanos , Masculino , Anopheles/classificação , Biodiversidade , Comportamento Alimentar/fisiologia , Insetos Vetores/classificação , Malária/transmissão , Anopheles/fisiologia , Mordeduras e Picadas de Insetos , Insetos Vetores/fisiologia , Estudos Longitudinais , Malária/epidemiologia , Densidade Demográfica , Fatores de Risco , Rios , Estações do Ano , Venezuela/epidemiologia
2.
Biochem Pharmacol ; 78(2): 162-70, 2009 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-19427997

RESUMO

Zalypsis is a new synthetic alkaloid tetrahydroisoquinoline antibiotic that has a reactive carbinolamine group. This functionality can lead to the formation of a covalent bond with the amino group of selected guanines in the DNA double helix, both in the absence and in the presence of methylated cytosines. The resulting complex is additionally stabilized by the establishment of one or more hydrogen bonds with adjacent nucleotides in the opposite strand as well as by van der Waals interactions within the minor groove. Fluorescence-based thermal denaturation experiments demonstrated that the most favorable DNA triplets for covalent adduct formation are AGG, GGC, AGC, CGG and TGG, and these preferences could be rationalized on the basis of molecular modeling results. Zalypsis-DNA adducts eventually give rise to double-strand breaks, triggering S-phase accumulation and apoptotic cell death. The potent cytotoxic activity of Zalypsis was ascertained in a 24 cell line panel. The mean IC(50) value was 7nM and leukemia and stomach tumor cell lines were amongst the most sensitive. Zalypsis administration in four murine xenograft models of human cancer demonstrates significant tumor growth inhibition that is highest in the Hs746t gastric cancer cell line with no weight loss of treated animals. Taken together, these results indicate that the potent antitumor activity of Zalypsis supports its current development in the clinic as an anticancer agent.


Assuntos
Antibióticos Antineoplásicos/farmacologia , Camundongos Nus , Neoplasias/tratamento farmacológico , Tetra-Hidroisoquinolinas/farmacologia , Animais , Antibióticos Antineoplásicos/química , Antibióticos Antineoplásicos/uso terapêutico , Linhagem Celular Tumoral , Dioxóis/química , Dioxóis/farmacologia , Dioxóis/uso terapêutico , Ensaios de Seleção de Medicamentos Antitumorais/métodos , Humanos , Camundongos , Tetra-Hidroisoquinolinas/química , Tetra-Hidroisoquinolinas/uso terapêutico , Trabectedina , Ensaios Antitumorais Modelo de Xenoenxerto/métodos
3.
Mol Cancer Ther ; 7(5): 1309-18, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18483318

RESUMO

Trabectedin (Yondelis; ET-743) is a potent anticancer drug that binds to DNA by forming a covalent bond with a guanine in one strand and one or more hydrogen bonds with the opposite strand. Using a fluorescence-based melting assay, we show that one single trabectedin-DNA adduct increases the thermal stability of the double helix by >20 degrees C. As deduced from the analysis of phosphorylated H2AX and Rad51 foci, we observed that clinically relevant doses of trabectedin induce the formation of DNA double-strand breaks in human cells and activate homologous recombination repair in a manner similar to that evoked by the DNA interstrand cross-linking agent mitomycin C (MMC). Because one important characteristic of this drug is its marked cytotoxicity on cells lacking a functional Fanconi anemia (FA) pathway, we compared the response of different subtypes of FA cells to MMC and trabectedin. Our data clearly show that human cells with mutations in FANCA, FANCC, FANCF, FANCG, or FANCD1 genes are highly sensitive to both MMC and trabectedin. However, in marked contrast to MMC, trabectedin does not induce any significant accumulation of FA cells in G2-M. The critical relevance of FA proteins in the response of human cells to trabectedin reported herein, together with observations showing the role of the FA pathway in cancer suppression, strongly suggest that screening for mutations in FA genes may facilitate the identification of tumors displaying enhanced sensitivity to this novel anticancer drug.


Assuntos
Antineoplásicos Alquilantes/farmacologia , Dioxóis/farmacologia , Proteínas de Grupos de Complementação da Anemia de Fanconi/genética , Tetra-Hidroisoquinolinas/farmacologia , Ciclo Celular , DNA/genética , DNA/metabolismo , Quebras de DNA de Cadeia Dupla , Reparo do DNA , Relação Dose-Resposta a Droga , Anemia de Fanconi/genética , Anemia de Fanconi/metabolismo , Proteínas de Grupos de Complementação da Anemia de Fanconi/metabolismo , Humanos , Mitomicina/farmacologia , Fatores de Tempo , Trabectedina
4.
J Med Chem ; 50(14): 3322-33, 2007 Jul 12.
Artigo em Inglês | MEDLINE | ID: mdl-17571868

RESUMO

The marine natural product thiocoraline A displayed approximately equal cytotoxic activity at nanomolar concentrations in a panel of 12 human cancer cell lines. X-ray diffraction analyses of orthorhombic crystals of this DNA-binding drug revealed arrays of docked pairs of staple-shaped molecules in which one pendent hydroxyquinoline chromophore from each cysteine-rich molecule appears intercalated between the two chromophores of a facing molecule. This arrangement is in contrast to the proposed mode of binding to DNA that shows the two drug chromophores clamping two stacked base pairs, in agreement with the nearest-neighbor exclusion principle. Proof of DNA sequence recognition was obtained from both classical DNase I footprinting experiments and determination of the melting temperatures of several custom-designed fluorescently labeled oligonucleotides. A rationale for the DNA-binding behavior was gained when models of thiocoraline clamping a central step embedded in several octanucleotides were built and studied by means of unrestrained molecular dynamics simulations in aqueous solution.


Assuntos
Antineoplásicos/farmacologia , DNA/metabolismo , Depsipeptídeos/farmacologia , Antineoplásicos/química , Antineoplásicos/metabolismo , Sequência de Bases , Linhagem Celular Tumoral , Cristalografia por Raios X , Pegada de DNA , Depsipeptídeos/química , Depsipeptídeos/metabolismo , Humanos , Estereoisomerismo
5.
J Med Chem ; 47(5): 1136-48, 2004 Feb 26.
Artigo em Inglês | MEDLINE | ID: mdl-14971893

RESUMO

New azaquinolizinium-type cations have been obtained from isochromane. The synthesis was completed over seven steps and included as the key feature an intramolecular Westphal condensation. This first example of the intramolecular process allowed the preparation of benzo[f]pyrido[2,1-a]phthalazinium and benzo[f]quino[2,1-a]phthalazinium salts, which were evaluated as DNA intercalators, DNA topoisomerase I inhibitors, and antiproliferative compounds. Both cationic systems behave as DNA intercalators and exhibit antiproliferative activity. The pentacyclic benzo[f]quino[2,1-a]phthalazinium cations also have an inhibitory effect on the catalytic activity of DNA topoisomerase I, without trapping of cleavage complexes. Structural characterization using density functional theory indicates that the fused ring systems are slightly nonplanar, and additional molecular modeling studies suggest a preferred orientation for the intercalating chromophores within a typical CpG or TpG intercalation site.


Assuntos
Antineoplásicos/síntese química , Substâncias Intercalantes/síntese química , Ftalazinas/síntese química , Antineoplásicos/química , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Resistência a Múltiplos Medicamentos , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Substâncias Intercalantes/química , Substâncias Intercalantes/farmacologia , Modelos Moleculares , Ftalazinas/química , Ftalazinas/farmacologia , Relação Estrutura-Atividade , Inibidores da Topoisomerase I
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