Síntese e avaliação da atividade citotóxica de derivados do eugenol contendo núcleos 1,2,3-triazólicos

Eugenol is an aromatic compound found in several plant species. It presents important biological activities including cytotoxicity. In this paper, it is described the synthesis and the evaluation of the cytotoxic activity of eugenol derivatives bearing 1,2,3-triazole functionalities. Eugenol, extracted via hydrodistillation from dried flower buds of Eugenia caryophyllata (=Syzygium aromaticum), was submitted to alkylation reactions to afford two terminal alkynes in good yields. The key reaction involved in the preparation of eugenol derivatives corresponded to the Copper(I)-catalyzed Azide-Alkyne Cycloaddition (CuAAC), between alkynylated eugenol derivatives and different benzyl azides. The evaluation of the cytotoxicity of twenty seven synthesized derivatives against HL60 leukemia cell line revealed that at 100 µmol L-1, five of them, namely 4-((4-allyl-2-methoxyphenoxy)methyl)-1-(3-bromobenzyl)-1H-1,2,3-triazole (6n), 4-(3-(4-allyl-2-methoxyphenoxy)propyl)-1-benzyl-1H-1,2,3-triazole (7a), 4-(3-(4-allyl-2-methoxyphenoxy)propyl)-1-(4-chlorobenzyl)-1H-1,2,3-triazole (7c), 4-(3-(4-allyl-2-methoxyphenoxy)propyl)-1-(4-iodobenzyl)-1H-1,2,3-triazole (7e) and 4-(3-(4-allyl-2-methoxyphenoxy)propyl)-1-(3-bromobenzyl)-1H-1,2,3-triazole (7m), were capable of significantly decreasing cell viability. These most active triazolic derivatives were also evaluated against B16F10 melanoma and Nalm6 leukemia cell lines. While only compound 7a was active against the former, compounds 6n, 7a, and 7m displayed activity against the latter. Derivative 7a was active against all cell lines. It is believed that eugenol derivatives bearing triazole functionalities may represent a scaffold to be explored toward the development of new agents against cancer

A genetic and virulence characterization of Brazilian strains of Mycoplasma hyopneumoniae

Mycoplasma hyopneumoniae (M. hyopneumoniae) is considered the primary causative agent of porcine enzootic pneumonia (EP), a chronic contagious respiratory disease that causes economic losses. Obtaining new pathogenic isolates and studying the genome and virulence factors are necessary. This study performed a complete sequencing analysis of two Brazilian strains, UFV01 and UFV02, aiming to characterize the isolates in terms of the virulence factors and sequence type. The complete genome analysis revealed the main virulence genes (mhp385, mhp271, MHP_RS03455, p102, p97, p216, MHP_RS00555, mhp107) and ST-123, the presence of three toxin-related genes (tlyC, PLDc_2 and hcnC), and some genetic groups specific to these two isolates. Subsequently, the pathogenicity of the isolates was evaluated via an experimental infection conducted in a swine model. The study was divided into three groups, namely a negative control group (n = 4) and two test groups (n = 8), totaling 20 animals. They were challenged at 35 days of age with 107 CCU (Color Changing Units) M. hyopneumoniae via the intratracheal route. The UFV01 group showed earlier and higher seroconversion (IgG) (100%), while only 50% of the UFV02 group seroconverted. The same trend was observed when analyzing the presence of IgA in the bronchoalveolar lavage fluid (BALF) at 35 days post-infection (dpi). The UFV01 group had a mean macroscopic lesion score of 11.75% at 35 dpi, while UFV02 had 3.125%. Microscopic lesions were more severe in the UFV01 group. Based on laryngeal swab samples evaluated by qPCR, and the detection began at 14 days. The UFV01 group showed 75% positivity at 14 dpi. The UFV02 group also started excreting at 14 dpi, with a positivity rate of 37.5%. The results indicate that the UFV01 isolate exhibits higher virulence than UFV02. These findings may aid in developing new vaccines and diagnostic kits and establishing experimental models for testing

Ki-1/57 is an intrinsically disordered protein involved in mechanisms of gene regulation

Orientador: Jorg KobargTese (doutorado) - Universidade Estadual de Campinas, Instituto e BiologiaResumo: A proteína Ki-1/57 foi descoberta através da reação cruzada do anticorpo monoclonal Ki-1 em células do linfoma de Hodgkin. Foi demonstrado previamente que Ki-1/57 sofre fosforilação por PKCs e metilação por PRMT1, uma arginino metiltransferase que modula diversas proteínas ligadoras a RNA. Nesse trabalho, é mostrada a interação de Ki-1/57 com sondas de RNA e com proteínas envolvidas no controle de splicing de pré-mRNA. O seu envolvimento no controle de splicing foi confirmado em ensaios de cotransfecção em células de mamíferos. Análises de microscopia de confocal mostraram a localização da construção EGFP-Ki-1/57 em diferentes corpúsculos nucleares de forma dependente da metilação celular. Essas regiões compreendem nucléolos, speckles, corpos de Cajal e GEMS, conhecidamente envolvidas na biogênese, maturação ou armazenamento de complexos de processamento de RNA/pré-RNA no núcleo. Análises a partir de construções truncadas sugeriram o N-terminal de Ki-1/57 como importante para a interação com proteínas reguladoras de splicing e localização nos corpúsculos nucleares, enquanto o C-terminal como necessário e suficiente para a ligação a RNA poliuridina e localização citoplasmática. Por outro lado, essas duas regiões pareceram atuar em conjunto no processamento do gene E1A. Similarmente a hnRNPQ, Ki-1/57 e outras proteínas funcionalmente relacionadas, SFRS9 é mostrada como alvo de metilação por PRMT1. A inibição da metilação resultou em um aumento do número de células apresentando localização da construção EGFP-SFRS9 no interior de nucléolos, mostrando a importância dessa modificação para a localização subnuclear de SFRS9. As características estruturais de Ki-1/57 também foram investigadas através de diferentes abordagens. Análises por SAXS, gel filtração analítica e ultracentrifugação analítica indicaram uma estrutura bastante alongada e flexível para a construção C-terminal 6xhis-(122-413)Ki-1/57. Ensaios de proteólise limitada também sugeriram uma baixa composição de núcleos hidrofóbicos estáveis e compactos. A capacidade de Ki-1/57 em sofrer enovelamento induzido após a interação com ligantes também foi monitorada em experimentos de dicroísmo circular. Embora não tenha sido observada nenhuma alteração estrutural após a incubação de 6xhis-(122-413)Ki-1/57 com o RNA poliuridina, a adição de TFE foi capaz de promover pequenos ganhos de elementos de estrutura secundária regular. Esses dados, juntamente com predições computacionais, sugerem que Ki-1/57 é uma nova proteína intrinsecamente desordenada, o que pode explicar o elevado número de diferentes proteínas parceiras que ela é capaz de interagir.Abstract: The Ki-1/57 protein has been discovered through the cross reactivity of the monoclonal antibody Ki-1 in Hodgkin lymphoma cells. Previously, it was demonstrated that Ki-1/57 undergoes phosphorylation by PKCs and methylation by PRMT1, an arginine methyltransferase that modulates many RNA binding proteins. Here, the interaction of Ki-1/57 with RNA polyuridine and proteins involved in pre-mRNA splicing control are shown. Its involvement in splicing regulation was confirmed by cotransfection assays in mammalian cells. Confocal microscopy analyses revealed the localization of EGFP-Ki-1/57 at different nuclear bodies, depending on the cellular methylation status. These regions include nucleoli, speckles, Cajal bodies and GEMS, which are all known to be involved in biogenesis, maturation or storing of RNA/pre-mRNA processing complexes in the nucleus. Analysis from experiments with truncated forms of Ki-1/57 suggested its N-terminus as important for its interaction with splicing proteins and localization at nuclear bodies. In turn, its C-terminus was seen as necessary and sufficient for the cytoplasmic localization and polyuridine RNA binding. However, these two regions seemed to be required working together for an efficient splicing activity on E1A gene. Similarly to hnRNPQ, Ki-1/57 and others functionally related proteins, SFRS9 is shown here as a target for methylation by PRMT1. The inhibition of this activity resulted in increase in the number of cells showing EGFP-SFRS9 in the nucleoli, suggesting the importance of methylation for the subnuclear localization of SFRS9. The structural characteristics of Ki-1/57 also have been investigated through different approaches. Analyses by SAXS, analytical gel filtration and analytical ultracentrifugation techniques suggested a very elongated and flexible structure for the C-terminal construct (122-413)Ki-1/57. Also, limited proteolysis analysis suggested a low composition of stable and compact hydrophobic cores. The ability of Ki-1/57 in suffering binding-induced folding was also investigated. Although no structural modification has been observed after incubating (122-413)Ki-1/57 with a polyuridine RNA, the addition of the TFE probe was able to promote a small gain of regular secondary structural elements. These findings, together with different computational predictions, pointed out that Ki-1/57 is a novel intrinsically unstructured protein. This could explain the wide array of protein partners with which it is able to interact.DoutoradoBioquimicaDoutor em Biologia Funcional e Molecula

Ácidos Graxos Trans: Alimentos e Efeitos na Saúde Trans fatty acids: foods and effects on health

Os ácidos graxos trans podem ser encontrados em alimentos obtidos a partir de animais ruminantes e em alimentos que contêm gordura vegetal parcialmente hidrogenada, como os "fast food". O consumo dos ácidos graxos trans é maior nos Estados Unidos, no Canadá e em países da Europa e menor no Japão e em países do Mediterrâneo. De forma semelhante, a incidência de doenças cardiovasculares são maiores naqueles países que apresentam um maior consumo. Os estudos demonstram que esses ácidos graxos podem contribuir para o aumento de LDL e de lipoproteína [a], além de reduzir os níveis de HDL. Ainda, os isômeros trans parecem inibir a ação de enzimas de dessaturação dos ácidos graxos essenciais (Δ5- e Δ6-dessaturase), inibindo a biossíntese de importantes ácidos graxos, como o ácido araquidônico e o ácido docosahexaenóico (DHA). Sobre a saúde materno-infantil, as concentrações de ácidos graxos trans ingeridos pela nutriz estão associadas às concentrações encontradas no leite materno. Além do leite, tais isômeros podem ser transferidos ao recém-nascido pela via placentária. Os estudos sugerem que os ácidos graxos trans afetariam o crescimento intra-uterino devido à inibição do metabolismo dos ácidos graxos essenciais, pelas enzimas dessaturases. A inibição dessas enzimas pode ser também um fator desencadeante de uma precoce lesão aterosclerótica. Porém, os efeitos dos ácidos graxos trans sobre a saúde ainda não são conclusivos e não existem recomendações para seu consumo. Além disso, no Brasil, os estudos para determinar o teor desses isômeros nos alimentos ainda são incipientes, o que demonstra uma grande necessidade de pesquisas nesta área.Trans fatty acids can be found in foods derived from ruminant animals and foods that contain partially hydrogenated fat such as fast foods. The consumption of trans fatty acids is larger in the United States, Canada, and some European countries than in Japan and Mediterranean countries. The incidence of coronary heart diseases is higher in countries where the consumption of trans fatty is high. Studies show that trans fatty acids can contribute to increase LDL and lipoprotein [a], and to reduce the levels of HDL. In addition, trans isomeric seems to inhibit the action of desaturase enzymes of essential fatty acids (Δ5- and Δ6-desaturase) by holding back the biosynthesis of important fatty acids such as arachidonic acid and docosahexaenoic acid (DHA). With respect to pregnant women’s and infant’s health, concentrations of trans fatty acids ingested by the mother are associated to concentrations found in the maternal milk. Besides the milk, the trans fatty acids can be transferred to the newly born through the placenta. Studies suggest that trans fatty acids can affect intra-uterine growth due to the inhibition of the conversion of essential fatty acids by desaturase enzymes. The inhibition of DHA can also cause early atherosclerosis lesion. However, studies on the effects of trans fatty acids on health are still inconclusive and there are no current recommendations on their consumption. Additionally, in Brazil, studies to determine the composition of trans isomeric in foods are still incipient, which indicates a great need of research in this area

Ácidos Graxos Trans: Alimentos e Efeitos na Saúde

Os ácidos graxos trans podem ser encontrados em alimentos obtidos a partir de animais ruminantes e em alimentos que contêm gordura vegetal parcialmente hidrogenada, como os "fast food". O consumo dos ácidos graxos trans é maior nos Estados Unidos, no Canadá e em países da Europa e menor no Japão e em países do Mediterrâneo. De forma semelhante, a incidência de doenças cardiovasculares são maiores naqueles países que apresentam um maior consumo. Os estudos demonstram que esses ácidos graxos podem contribuir para o aumento de LDL e de lipoproteína [a], além de reduzir os níveis de HDL. Ainda, os isômeros trans parecem inibir a ação de enzimas de dessaturação dos ácidos graxos essenciais (Δ5- e Δ6-dessaturase), inibindo a biossíntese de importantes ácidos graxos, como o ácido araquidônico e o ácido docosahexaenóico (DHA). Sobre a saúde materno-infantil, as concentrações de ácidos graxos trans ingeridos pela nutriz estão associadas às concentrações encontradas no leite materno. Além do leite, tais isômeros podem ser transferidos ao recém-nascido pela via placentária. Os estudos sugerem que os ácidos graxos trans afetariam o crescimento intra-uterino devido à inibição do metabolismo dos ácidos graxos essenciais, pelas enzimas dessaturases. A inibição dessas enzimas pode ser também um fator desencadeante de uma precoce lesão aterosclerótica. Porém, os efeitos dos ácidos graxos trans sobre a saúde ainda não são conclusivos e não existem recomendações para seu consumo. Além disso, no Brasil, os estudos para determinar o teor desses isômeros nos alimentos ainda são incipientes, o que demonstra uma grande necessidade de pesquisas nesta área

Ki-1/57 and CGI-55 ectopic expression impact cellular pathways involved in proliferation and stress response regulation

Ki-1/57 (HABP4) and CGI-55 (SERBP1) are regulatory proteins and paralogs with 40.7% amino acid sequence identity and 67.4% similarity. Functionally, they have been implicated in the regulation of gene expression on both the transcriptional and mRNA metabolism levels. A link with tumorigenesis is suggested, since both paralogs show altered expression levels in tumor cells and the Ki-1/57 gene is found in a region of chromosome 9q that represents a haplotype for familiar colon cancer. However, the target genes regulated by Ki-1/57 and CGI-55 are unknown. Here, we analyzed the alterations of the global transcriptome profile after Ki-1/57 or CGI-55 overexpression in HEK293T cells by DNA microchip technology. We were able to identify 363 or 190 down-regulated and 50 or 27 up-regulated genes for Ki-1/57 and CGI-55, respectively, of which 20 were shared between both proteins. Expression levels of selected genes were confirmed by qRT-PCR both after protein overexpression and siRNA knockdown. The majority of the genes with altered expression were associated to proliferation, apoptosis and cell cycle control processes, prompting us to further explore these contexts experimentally. We observed that overexpression of Ki-1/57 or CGI-55 results in reduced cell proliferation, mainly due to a G1 phase arrest, whereas siRNA knockdown of CGI-55 caused an increase in proliferation. In the case of Ki-1/57 overexpression, we found protection from apoptosis after treatment with the ER-stress inducer thapsigargin. Together, our data give important new insights that may help to explain these proteins putative involvement in tumorigenic event

Evidence for the association of the human regulatory protein Ki-1/57 with the translational machinery

Ki-1/57 is a cytoplasmic and nuclear protein of 57 kDa first identified in malignant cells from Hodgkin’s lymphoma. Based on yeast-two hybrid protein interaction we found out that Ki-1/57 interacts with adaptor protein RACK1 (receptor of activated kinase 1), CIRP (cold-inducible RNA-binding protein), RPL38 (ribosomal protein L38) and FXR1 (fragile X mental retardation-related protein 1). Since these proteins are involved in the regulation of translation we suspected that Ki-1/57 may have a role in it. We show by immunoprecipitation the association of Ki-1/57 with FMRP. Confocal microscopy revealed that Ki-1/57 colocalizes with FMRP/FXR1/2 to stress granules. Furthermore Ki-1/57 cosediments with free ribosomal particles and enhances translation, when tethered to a reporter mRNA, suggesting that Ki-1/57 may be involved in translational regulation

Ki-1/57 And Cgi-55 Ectopic Expression Impact Cellular Pathways Involved In Proliferation And Stress Response Regulation.

Ki-1/57 (HABP4) and CGI-55 (SERBP1) are regulatory proteins and paralogs with 40.7% amino acid sequence identity and 67.4% similarity. Functionally, they have been implicated in the regulation of gene expression on both the transcriptional and mRNA metabolism levels. A link with tumorigenesis is suggested, since both paralogs show altered expression levels in tumor cells and the Ki-1/57 gene is found in a region of chromosome 9q that represents a haplotype for familiar colon cancer. However, the target genes regulated by Ki-1/57 and CGI-55 are unknown. Here, we analyzed the alterations of the global transcriptome profile after Ki-1/57 or CGI-55 overexpression in HEK293T cells by DNA microchip technology. We were able to identify 363 or 190 down-regulated and 50 or 27 up-regulated genes for Ki-1/57 and CGI-55, respectively, of which 20 were shared between both proteins. Expression levels of selected genes were confirmed by qRT-PCR both after protein overexpression and siRNA knockdown. The majority of the genes with altered expression were associated to proliferation, apoptosis and cell cycle control processes, prompting us to further explore these contexts experimentally. We observed that overexpression of Ki-1/57 or CGI-55 results in reduced cell proliferation, mainly due to a G1 phase arrest, whereas siRNA knockdown of CGI-55 caused an increase in proliferation. In the case of Ki-1/57 overexpression, we found protection from apoptosis after treatment with the ER-stress inducer thapsigargin. Together, our data give important new insights that may help to explain these proteins putative involvement in tumorigenic events.18432944-5