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1.
Biochim Biophys Acta Rev Cancer ; 1868(1): 333-340, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28554667

ABSTRACT

Glioblastoma, the most aggressive and fatal type of brain tumor, is capable of interacting with brain immune cells such as microglia, which contributes to the growth of these tumors. Various molecules, including growth factors and cytokines, have been identified as regulators of microglia-glioblastoma interaction. Recent studies suggest that the Wnt family of lipoglycoproteins plays an important role, not only in biological events during development, but also in cancer progression, and can be part of microglia recruitment to glioblastoma as well as of tumor growth and invasion. Here, we discuss recent interesting findings that support a role for Wnt signaling pathways in the microglia-glioblastoma crosstalk.


Subject(s)
Brain Neoplasms/metabolism , Glioblastoma/metabolism , Microglia/metabolism , Wnt Signaling Pathway/physiology , Animals , Brain Neoplasms/pathology , Cytokines/metabolism , Glioblastoma/pathology , Humans , Intercellular Signaling Peptides and Proteins/metabolism , Microglia/pathology
2.
Arq. bras. med. vet. zootec ; 66(6): 1779-1786, 12/2014. tab
Article in Portuguese | LILACS | ID: lil-735759

ABSTRACT

Objetivou-se avaliar o consumo de forragem e o desempenho de ovinos mantidos em pastagem de capim-aruana, submetidos a porcentagens crescentes de proteína bruta (PB) no suplemento, na época seca. Vinte borregos da raça Santa Inês foram utilizados em delineamento inteiramente ao acaso, com cinco tratamentos e quatro repetições. Os suplementos foram fornecidos em 1,0% do peso corporal, nas porcentagens de 0, 15, 20, 25 e 30%. O aumento de proteína bruta influenciou o consumo total de matéria seca (kg/dia) e a porcentagem do peso vivo, com valores máximos estimados de 1.296g (3,2% de MS) com 21,48 e 21,89% de PB no suplemento, respectivamente. O consumo de forragem máximo, estimado de 893g/dia, ocorreu com a PB de 21,5%. O aumento de PB nos suplementos resultou em efeito quadrático sobre o ganho médio diário, com valor máximo de 104g/dia com a PB de 23% no suplemento. Recomenda-se o uso de suplementos múltiplos com 21 a 23% de PB fornecidos na proporção de 1% do peso corporal (PC) para ovinos mantidos em pastos de capim-aruana na época seca...


The aim of this study was to evaluate the forage intake and grazing sheep performance keep on Aruana grass subjected to increasing crude protein (CP) levels in the supplement on dry season. Twenty Santa Ines male lambs were used, with initial body weight of 31.80kg by a completely randomized design with five treatments and four replications. The supplements were provided daily at 1% of body weight, with protein levels of 0, 15, 20, 25 and 30%. The increase of the crude protein levels promoted a squarely effect on dry matter intake (kg/day and % of BW), with maximum estimated values of 1296g and 3.2% of DM in CP levels of 21.48 and 21.89, respectively. The maximum forage intake estimated of 893g/day occurred in CP level de 21.51%. The increased of crude protein level in supplements increased squarely the average daily gain, with a maximum of 104g/day, for the 23% crude protein in the supplement. Thus, the use of the multiple supplements supplied in 1% of body weight with CP levels ranged 21 a 23% is indicated for sheep grazing Aruana grass on dry season...


Subject(s)
Animals , Abattoirs , Food Additives/analysis , Biotechnology , Chickens , Carotenoids/administration & dosage , Antioxidants/analysis , Pigmentation/physiology , Xanthophylls/adverse effects
3.
Arq. bras. med. vet. zootec ; 63(4): 954-961, ago. 2011. tab
Article in Portuguese | LILACS | ID: lil-599616

ABSTRACT

Avaliou-se a composição química e a resistência óssea do tibiotarso de frangos de corte aos 21 dias de idade. Foram determinados os percentuais ósseos de proteínas colagenosas (PC) e proteínas não colagenosas (PNC) e de cálcio, fósforo, potássio e sódio. Foram utilizados 650 pintinhos machos de marca comercial, alimentados com dietas à base de milho e farelo de soja. Foi utilizado delineamento em blocos ao acaso com cinco repetições e 26 aves por unidade experimental. Os tratamentos consistiram na suplementação da dieta basal com NH4Cl a fim de se obter cinco níveis -50; 0; 50; 100 e 150mEq/kg de balanço eletrolítico (BE). O nível de BE influenciou os teores de fósforo, potássio, sódio, PC e PNC, relação Ca:P e a resistência à quebra. A redução do balanço eletrolítico da dieta em nível inferior a 150mEq/kg influenciará negativamente a mineralização e a resistência óssea. A resistência à quebra do tibiotarso não está correlacionada com as concentrações dos minerais de forma individual, mas correlaciona-se negativamente com as concentrações de proteínas colagenosas e não colagenosas.


This study was carried out in order to evaluate the bone chemical composition and breaking force resistance of tibiotarsus birds at 21 days of age. The bone percentage of colagenous proteins (CP), non colagenous proteins (NCP) and minerals (calcium, phosphorus, potassium and sodium) was analyzed. A total of 650 commercial male broiler chicks were fed corn and soybean diets. A completely randomized block design with five replications of 26 birds per experimental unit was used. The treatments consisted of the basal ration supplemented with NH4Cl in order to obtain five levels (-50; 0; 50; 100 and 150mEq/kg) of electrolyte balance. The EB level affected the percentages of phosphorus, potassium and sodium, PC and PNC, Ca: P relation and breaking force resistance. The reduction of EB diets at levels below 150mEq/kg will affect negatively the mineralization and bone resistance. The breaking force of tibiotarsus is not correlated with the mineral concentration individually, but correlates negatively with the concentration of collagenous and non-collagenous proteins.


Subject(s)
Animals , Female , Bone Density , Enzyme Activation , Electrolytes/metabolism , Chickens/growth & development , Ketosis , Osteogenesis , Anions , Calcium , Collagen/metabolism , Diet , Phosphorus , Potassium , Proteins/metabolism , Sodium
4.
Braz. j. med. biol. res ; 44(3): 200-205, Mar. 2011. ilus, tab
Article in English | LILACS | ID: lil-576062

ABSTRACT

Connective tissue growth factor (CCN2/CTGF) is a matricellular-secreted protein involved in extracellular matrix remodeling. The P19 cell line is an embryonic carcinoma line widely used as a cellular model for differentiation and migration studies. In the present study, we employed an exogenous source of CCN2 and small interference RNA to address the role of CCN2 in the P19 cell aggregation phenomenon. Our data showed that increasing CCN2 protein concentrations from 0.1 to 20 nM decreased the number of cell clusters and dramatically increased cluster size without changing proliferation or cell survival, suggesting that CCN2 induced aggregation. In addition, CCN2 specific silencing inhibited typical P19 cell aggregation, which could be partially rescued by 20 nM CCN2. The present study demonstrates that CCN2 is a key molecule for cell aggregation of embryonic P19 cells.


Subject(s)
Humans , Cell Aggregation/drug effects , Cell Proliferation/drug effects , Connective Tissue Growth Factor/pharmacology , Embryonal Carcinoma Stem Cells/drug effects , Cell Adhesion , Cell Line, Tumor , Cell Survival/drug effects , Cell Survival/physiology
5.
Braz J Med Biol Res ; 44(3): 200-5, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21344133

ABSTRACT

Connective tissue growth factor (CCN2/CTGF) is a matricellular-secreted protein involved in extracellular matrix remodeling. The P19 cell line is an embryonic carcinoma line widely used as a cellular model for differentiation and migration studies. In the present study, we employed an exogenous source of CCN2 and small interference RNA to address the role of CCN2 in the P19 cell aggregation phenomenon. Our data showed that increasing CCN2 protein concentrations from 0.1 to 20 nM decreased the number of cell clusters and dramatically increased cluster size without changing proliferation or cell survival, suggesting that CCN2 induced aggregation. In addition, CCN2 specific silencing inhibited typical P19 cell aggregation, which could be partially rescued by 20 nM CCN2. The present study demonstrates that CCN2 is a key molecule for cell aggregation of embryonic P19 cells.


Subject(s)
Cell Aggregation/drug effects , Cell Proliferation/drug effects , Connective Tissue Growth Factor/pharmacology , Embryonal Carcinoma Stem Cells/drug effects , Cell Adhesion , Cell Line, Tumor , Cell Survival/drug effects , Cell Survival/physiology , Humans
6.
Biomed Pharmacother ; 64(1): 63-72, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19864107

ABSTRACT

B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is the most common malignancy in children. The Wnt signaling pathway has been found to be extensively involved in cancer onset and progression but its role in BCP-ALL remains controversial. We evaluate the role of the Wnt pathway in maintenance of BCP-ALL cells and resistance to chemotherapy. Gene expression profile revealed that BCP-ALL cells are potentially sensitive to modulation of Wnt pathway. Nalm-16 and Nalm-6 cell lines displayed low levels of canonical activation, as reflected by the virtually complete absence of total beta-catenin in Nalm-6 and the beta-catenin cell membrane distribution in Nalm-16 cell line. Canonical activation with Wnt3a induced nuclear beta-catenin translocation and led to BCP-ALL cell death. Lithium chloride (LiCl) also induced a cytotoxic effect on leukemic cells. In contrast, both Wnt5a and Dkk-1 increased Nalm-16 cell survival. Also, Wnt3a enhanced the in vitro sensitivity of Nalm-16 to etoposide (VP-16) while treatment with canonical antagonists protected leukemic cells from chemotherapy-induced cell death. Overall, our results suggest that canonical activation of the Wnt pathway may exerts a tumor suppressive effect, thus its inhibition may support BCP-ALL cell survival.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Etoposide/pharmacology , Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Wnt Proteins/metabolism , Cell Death/drug effects , Cell Line, Tumor , Cell Survival/drug effects , Drug Resistance, Neoplasm/drug effects , Gene Expression Regulation, Neoplastic , Humans , Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/physiopathology , Protein Transport , Signal Transduction , beta Catenin/metabolism
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