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	Provedor de dados BJMBR (1) International Journal of Morphology (1) J. Venom. Anim. Toxins incl. Trop. Dis. (1) Autor Abreu,R.B.V. (1) Adefolaju,Gbenga Anthony (1) Attarde,Saurabh S. (1) Freitas-Alves,D.R. (1) Hosie,Margot Jill (1) Pandit,Sangeeta V. (1) Piranda,D.N. (1) Scholtz,Kathrine Elizabeth (1) Vianna-Jorge,R. (1) de Carvalho,M.A. (1) Mais... Palavra-chave MCF-7 (3) Breast cancer (2) Anticancer (1) COX-2 (1) GNP-NN-32 (1) Gene expression (1) HEK293FT (1) Haplotypes (1) MCF-10A (1) MDA-MB-231 (1) Naja naja (1) PTGS2 (1) Protease Inhibitors (1) Reverse Transcriptase Inhibitors (1) Toxin (1) VEGF165b (1) Venom (1) Mais... Tipo do documento Info:eu-repo/semantics/article (2) Journal article (1) Ano 2020 (1) 2018 (1) 2017 (1) País Brazil (2) Chile (1) Idioma Inglês (3)		Ordenar por:  Relevância Autor Título Ano Registros recuperados: 3 Primeira ... 1 ... Última Antiangiogenic VEGF165b Expression in Human Breast MCF-7 and MCF-10A Cells Exposed to Reverse Transcriptase and Protease Inhibitors International Journal of Morphology Adefolaju,Gbenga Anthony; Scholtz,Kathrine Elizabeth; Hosie,Margot Jill. The combined antiretroviral therapy (cART), a multidrug combination regimen, usually consisting Nucleoside Reverse Transcriptase Inhibitors, non- Nucleoside Reverse Transcriptase Inhibitors and Protease Inhibitors has altered the morbidity pattern affecting HIV-infected individuals to include non-AIDS-defining malignancies (nADMs). The speculation is rife; does cART induce or promote the progression of nADMs such as breast cancer? This study was therefore designed to investigate of the effects of some antiretroviral drugs (at clinically relevant concentrations) on the expression of anti-angiogenic gene; VEGF165b in two human breast cell lines; MCF-7 and MCF-10A by Real Time qPCR and immuno-fluorescence. All of the antiretroviral drugs and combinations... Tipo: Journal article Palavras-chave: Reverse Transcriptase Inhibitors; Protease Inhibitors; VEGF165b; Breast cancer; MCF-7; MCF-10A. Ano: 2017 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022017000100024 Anticancer potential of nanogold conjugated toxin GNP-NN-32 from Naja naja venom J. Venom. Anim. Toxins incl. Trop. Dis. Attarde,Saurabh S.; Pandit,Sangeeta V.. Abstract Background: Cancer is the second most common fatal disease in the world, behind cardiovascular disorders in the first place. It accounts for around 0.3 million deaths per year in India due to the lack of proper diagnostic facilities, prevention and treatment. Current therapeutic methods do not provide adequate protection and affect normal cells along with cancerous ones. Thus, there is a need for some alternative therapeutic strategy, preferably from natural products, which have been traditionally used for treatment of various diseases in the country. Methods: In this study, we have conjugated purified NN-32 toxin from Naja naja venom with gold nanoparticles and its anticancer potential was evaluated against human breast cancer cell lines.... Tipo: Info:eu-repo/semantics/article Palavras-chave: GNP-NN-32; Anticancer; Toxin; Naja naja; Venom; Breast cancer; MCF-7; MDA-MB-231. Ano: 2020 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992020000100304 Modulation of the prostaglandin-endoperoxide synthase 2 gene expression by variant haplotypes: influence of the 3′-untranslated region BJMBR Piranda,D.N.; Abreu,R.B.V.; Freitas-Alves,D.R.; de Carvalho,M.A.; Vianna-Jorge,R.. The inducible inflammatory enzyme cycloxigenase-2 is up-regulated in cancer, and favors tumor progression. Cycloxigenase-2 is encoded by the prostaglandin-endoperoxide synthase 2 (PTGS2) gene, which presents sequence variations in the promoter region (PR) and in the 3′-untranslated region (3′-UTR). Different PR (rs689465, rs689466, rs20417) and 3′-UTR (rs5275) variants were generated by site-directed mutagenesis, and combined in haplotypes to access expression levels using a reporter system (luciferase) in human cells (MCF-7 and HEK293FT). Luciferase activity did not differ significantly among PTGS2 PR constructs, except for pAAC (containing variant allele rs20417 C), with 40% less activity than pAAG (wild-type sequence) in MCF-7 cells (P<0.01). Despite... Tipo: Info:eu-repo/semantics/article Palavras-chave: COX-2; PTGS2; Haplotypes; Gene expression; MCF-7; HEK293FT. Ano: 2018 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2018000200602 Registros recuperados: 3 Primeira ... 1 ... Última

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