Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 106
Filtrar
Mais filtros

País/Região como assunto
Tipo de documento
Intervalo de ano de publicação
1.
Apoptosis ; 28(1-2): 186-198, 2023 02.
Artigo em Inglês | MEDLINE | ID: mdl-36282364

RESUMO

BACKGROUND: LACTB was recently identified as a mitochondrial tumour suppressor that negatively affects cancer cell proliferation by inducing cell death and/or differentiation, depending on the cell type and tissue. However, the detailed mechanism underlying the LACTB-induced cancer cell death is largely unknown. METHODS: We used cell-based, either in 2D or 3D conditions, and in vivo experiments to understand the LACTB mechanisms. In this regard, protein array followed by an enrichment analysis, cell proliferation assays using different compounds, western blot analysis, flow cytometry and immunofluorescence were performed. Differences between quantitative variables following normal distribution were valuated using Student t test for paired or no-paired samples according to the experiment. For in vivo experiments differences in tumour growth were analyzed by 2-way ANOVA. RESULTS: We show, that LACTB expression leads to cell cycle arrest in G1 phase and increase of DNA oxidation that leads to activation of intrinsic caspase-independent cell death pathway. This is achieved by an increase of mitochondrial reactive oxygen species since early time points of LACTB induction. CONCLUSION: Our work provides a deeper mechanistic insight into LACTB-mediated cancer-cell death and shows the dynamics of the cellular responses a particular tumor suppressive stimulus might evoke under different genetic landscapes.


Assuntos
Neoplasias da Mama , Caspases , Humanos , Feminino , Caspases/genética , Caspases/metabolismo , Apoptose/genética , Neoplasias da Mama/genética , Neoplasias da Mama/metabolismo , Linhagem Celular Tumoral , Pontos de Checagem do Ciclo Celular , Espécies Reativas de Oxigênio/metabolismo , beta-Lactamases/genética , beta-Lactamases/metabolismo , Proteínas de Membrana/genética , Proteínas Mitocondriais/genética
2.
Pediatr Dermatol ; 40(6): 1104-1106, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37219506

RESUMO

CARD14-associated papulosquamous eruption (CAPE) is a rare inflammatory skin eruption that can have features of psoriasis, pityriasis rubra pilaris, and erythroderma. This skin condition is known for its resistance to topical or conventional systemic therapies. Successful treatment of CAPE with anti-IL-12/IL-23 and IL-17 inhibitors has been reported. We present a case of a 2-year-old girl with CAPE who was successfully treated with ustekinumab.


Assuntos
Dermatite Esfoliativa , Fármacos Dermatológicos , Pitiríase Rubra Pilar , Psoríase , Criança , Feminino , Humanos , Pré-Escolar , Ustekinumab/uso terapêutico , Fármacos Dermatológicos/uso terapêutico , Pitiríase Rubra Pilar/tratamento farmacológico , Psoríase/tratamento farmacológico , Guanilato Ciclase , Proteínas de Membrana , Proteínas Adaptadoras de Sinalização CARD
3.
Molecules ; 28(2)2023 Jan 11.
Artigo em Inglês | MEDLINE | ID: mdl-36677786

RESUMO

The increasing demand for superfoods has resulted in an increase in chia seeds consumption. The reintroduction of this ancient crop in agriculture is useful to ensure food security since it can grow in high-stress conditions. The current study aimed to characterize chia seeds, cold-pressed oil, and defatted cake (the oil extraction by-product) to improve their value and to meet consumer's expectations (low-fat products). Chia seeds presented a significantly higher energy value than cake (444 vs. 284 kcal/100 g, respectively) due to fat removal (33 vs. 7%). The cake showed higher contents of total minerals (6 vs. 5%), protein (27 vs. 18%), and fiber (48 vs. 38%) in comparison to the seeds, and was hence considered a promising food ingredient. The major fatty acid in oil, seeds, and cake was α-linolenic acid (62-66%), and the vitamin E content was 409, 200, and 44 mg/kg, respectively. The major amino acid in the seeds and cake was glutamic acid (49 vs. 36 mg/g). The oil had a low oxidative stability (1 h), and the total phenolics content was 1.3 mg gallic acid equivalents/100 g. Chia cake incorporation in food formulations will follow consumer's interests, and the obtained oil can be used to improve the oil supply for different applications. This approach adds value to the concept of "one health" since it includes the culture, the environment, and the consumers.


Assuntos
Salvia , Sementes , Sementes/química , Extratos Vegetais/análise , Ácidos Graxos/análise , Grão Comestível/metabolismo , Óleos de Plantas/química , Salvia/química
4.
Molecules ; 28(6)2023 Mar 22.
Artigo em Inglês | MEDLINE | ID: mdl-36985848

RESUMO

Olive pomace is a by-product from olive oil production that can be further processed to obtain olive pomace paste. In this work, the influence of different time/temperature binomials (65 °C/30 min; 77 °C/1 min; 88 °C/15 s; and 120 °C/20 min) on the nutritional quality, chemical composition, and efficiency on control/elimination of natural microbial load of olive pomace paste was ascertained. The treatments significantly impacted the contents of ash, fat, vitamin E, phenolics (including hydroxytyrosol), flavonoids, and antioxidant activity, but not the fatty acids profile. The binomial 88 °C/15 s showed the greatest potential since it better preserved the phytochemical and antioxidant properties as well as the protein and fiber contents. This binomial is also faster and easy to be implemented at an industrial level, allowing the obtention of a safe functional ingredient to satisfy consumers' demands for novel sustainable products, simultaneously, responding to food safety and food security concerns.


Assuntos
Antioxidantes , Olea , Antioxidantes/farmacologia , Olea/química , Temperatura , Azeite de Oliva , Vitamina E
5.
J Cutan Pathol ; 47(11): 1073-1075, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32716598

RESUMO

Uncombable hair syndrome is a rare disorder of the hair shaft that leads to silvery and unruly hair. The hair shaft anomaly is characterized by a longitudinal groove that is detected by scanning electronic microscopy-considered to be the gold standard for diagnosis. Recently, hair cross-sectioning has been reported as a viable alternative, but currently available methods still have some flaws, especially because of hair samples' processing specificities. Here, we present two cases of uncombable hair syndrome and a new embedding technique using epoxy to perform the diagnosis.


Assuntos
Doenças do Cabelo/diagnóstico , Doenças do Cabelo/patologia , Técnicas de Preparação Histocitológica/métodos , Pré-Escolar , Compostos de Epóxi , Feminino , Humanos
6.
Nucleic Acids Res ; 46(D1): D788-D793, 2018 01 04.
Artigo em Inglês | MEDLINE | ID: mdl-29045725

RESUMO

Transcriptomic data have become a fundamental resource for stem cell (SC) biologists as well as for a wider research audience studying SC-related processes such as aging, embryonic development and prevalent diseases including cancer, diabetes and neurodegenerative diseases. Access and analysis of the growing amount of freely available transcriptomics datasets for SCs, however, are not trivial tasks. Here, we present StemMapper, a manually curated gene expression database and comprehensive resource for SC research, built on integrated data for different lineages of human and mouse SCs. It is based on careful selection, standardized processing and stringent quality control of relevant transcriptomics datasets to minimize artefacts, and includes currently over 960 transcriptomes covering a broad range of SC types. Each of the integrated datasets was individually inspected and manually curated. StemMapper's user-friendly interface enables fast querying, comparison, and interactive visualization of quality-controlled SC gene expression data in a comprehensive manner. A proof-of-principle analysis discovering novel putative astrocyte/neural SC lineage markers exemplifies the utility of the integrated data resource. We believe that StemMapper can open the way for new insights and advances in SC research by greatly simplifying the access and analysis of SC transcriptomic data. StemMapper is freely accessible at http://stemmapper.sysbiolab.eu.


Assuntos
Linhagem da Célula , Bases de Dados Genéticas , Expressão Gênica , Células-Tronco , Astrócitos/citologia , Coleta de Dados , Curadoria de Dados , Conjuntos de Dados como Assunto , Humanos , Células-Tronco Neurais/citologia , Análise de Componente Principal , Células-Tronco/citologia , Células-Tronco/metabolismo , Interface Usuário-Computador , Fluxo de Trabalho
7.
Molecules ; 25(5)2020 Mar 03.
Artigo em Inglês | MEDLINE | ID: mdl-32138318

RESUMO

This study aimed to develop new canned chub mackerel products incorporating edible seaweeds (Ascophyllum nodosum, Fucus spiralis, Saccorhiza polyschides, Chondrus crispus, Porphyra sp. and Ulva sp.) harvested in the Portuguese North-Central coast, with simultaneous sensory improvement and minerals enrichment. Two processes were compared, namely the addition of seaweeds in i) the canning step and ii) in the brining step (as the replacement for salt). The concentrations of four macrominerals (Na, K, Ca and Mg), chloride, and twelve trace elements (Co, Cu, Fe, I, Li, Mn, Mo, Rb, Se, Sr, V and Zn) were determined by high-resolution continuum source flame atomic absorption spectrometry (HR-CS-FAAS) and inductively coupled plasma mass spectrometry (ICP-MS), respectively. Results showed that canned chub mackerel incorporating C. crispus and F. spiralis was found to be the preferred sensory option, also exhibiting contents enriched with Cl, Co, Cu, Fe, I, Li, Mg, Mn, Mo, Na, Rb, Se, and Sr. This effect was more pronounced when both seaweed species were added to replace the salt added in the brining step.


Assuntos
Minerais/análise , Perciformes , Alga Marinha , Oligoelementos/análise , Animais , Espectrofotometria Atômica
10.
J Paediatr Child Health ; 59(4): 702, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-35708246
13.
Nucleic Acids Res ; 43(W1): W72-7, 2015 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-26007653

RESUMO

Stem cells present unique regenerative abilities, offering great potential for treatment of prevalent pathologies such as diabetes, neurodegenerative and heart diseases. Various research groups dedicated significant effort to identify sets of genes-so-called stemness signatures-considered essential to define stem cells. However, their usage has been hindered by the lack of comprehensive resources and easy-to-use tools. For this we developed StemChecker, a novel stemness analysis tool, based on the curation of nearly fifty published stemness signatures defined by gene expression, RNAi screens, Transcription Factor (TF) binding sites, literature reviews and computational approaches. StemChecker allows researchers to explore the presence of stemness signatures in user-defined gene sets, without carrying-out lengthy literature curation or data processing. To assist in exploring underlying regulatory mechanisms, we collected over 80 target gene sets of TFs associated with pluri- or multipotency. StemChecker presents an intuitive graphical display, as well as detailed statistical results in table format, which helps revealing transcriptionally regulatory programs, indicating the putative involvement of stemness-associated processes in diseases like cancer. Overall, StemChecker substantially expands the available repertoire of online tools, designed to assist the stem cell biology, developmental biology, regenerative medicine and human disease research community. StemChecker is freely accessible at http://stemchecker.sysbiolab.eu.


Assuntos
Software , Células-Tronco/metabolismo , Animais , Sítios de Ligação , Diferenciação Celular/genética , Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/metabolismo , Perfilação da Expressão Gênica , Humanos , Internet , Camundongos , Neoplasias Pancreáticas/genética , Neoplasias Pancreáticas/metabolismo , Interferência de RNA , Fatores de Transcrição/metabolismo
16.
Pediatr Dermatol ; 34(5): 578-583, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28730603

RESUMO

BACKGROUND: Hidradenitis suppurativa (HS) is rare in childhood, with only 2% of cases in patients younger than 11 years. It is a chronic, recurrent, debilitating condition for which no universally effective treatment has been developed. We present five cases of children with HS diagnosed between the ages of 6 and 11 years. METHODS: Patients were treated with oral finasteride 1 to 5 mg/day. All had entered puberty at the time of treatment initiation. All had normal laboratory results before starting treatment. The maximum duration of treatment was 24 months. RESULTS: Four patients were female. Two were overweight. Three had been previously treated with oral antibiotics, and two of these with oral isotretinoin, with partial or no improvement. Overall improvement of the disease was observed in all patients, with a reduction of the frequency and intensity of the flares. No adverse effects were observed or reported during treatment. CONCLUSION: Treatment of HS can be challenging. The options available include antimicrobials, immunosuppressants, hormonal therapies, lasers, and surgery. The authors report the largest series of children with HS treated with finasteride. The results support the use of finasteride as monotherapy for the treatment of this disease in children. Further studies are necessary to fully understand the role of this drug in the management of this disease.


Assuntos
Inibidores de 5-alfa Redutase/uso terapêutico , Finasterida/uso terapêutico , Hidradenite Supurativa/tratamento farmacológico , Adolescente , Criança , Feminino , Humanos , Masculino , Resultado do Tratamento
17.
Dermatol Online J ; 23(4)2017 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-28541875

RESUMO

Infantile myofibromatosis is a rare disorder of fibroblastic/myofibroblastic proliferation and represents the most frequent type of mesenchymal tumor in the neonatal period and primary infancy.Three clinical types have been described: solitary, multicentric, and generalized (with visceral involvement). A correct characterization of the histopathology is essential to diagnose these neoplasias in early infancy. We present a case of multicentric infantile myofibromatosis with regression over time.


Assuntos
Miofibromatose/congênito , Regressão Neoplásica Espontânea , Feminino , Humanos , Lactente , Miofibromatose/diagnóstico , Miofibromatose/patologia
18.
Dermatol Online J ; 23(7)2017 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-29469702

RESUMO

Bullous pemphigoid (BP) is an immune mediated bullous disease that is manifested by urticarial plaques with superimposed subepidermal blisters and significant pruritus. It is generally found in the elderly, but is rare in the pediatric population. A 5-month-old girl previously diagnosed with hand-foot-mouth disease was examined in our dermatology department owing to vesicles and bullae, initially located to the hands and feet, which progressed with new lesions. Tense vesicles and bullae distributed in an annular string of pearls pattern on the abdomen and facial and cervical regions were noted. Histologic and immunologic findings were consistent with the diagnosis of infantile BP. Disease control was obtained with oral prednisolone and dapsone; the patient was still in clinical remission 6 months after treatment cessation. The differential diagnosis of the clinical presentation of the lesions in our patient is of note, given that this blistering pattern is frequently reported in association with linear IgA bullous dermatosis.


Assuntos
Penfigoide Bolhoso/patologia , Diagnóstico Diferencial , Erros de Diagnóstico , Feminino , Doença de Mão, Pé e Boca/diagnóstico , Humanos , Lactente , Penfigoide Bolhoso/diagnóstico , Pele/patologia
19.
Dermatol Online J ; 23(3)2017 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-28329526

RESUMO

Chronic granulomatous disease (CGD) is a primaryimmunodeficiency disorder that affects the phagocyticcells of the innate immune system. It is characterizedby recurrent or persistent infections with granulomaformation. Lupus-like lesions have been reported incarriers of CGD and less frequently, in patients withCGD. Immunological study in these patients areusually negative. We describe the case of an 8-yearoldboy with CGD who developed chronic and acutecutaneous lupus erythematous with angular cheilitis,oral ulcers, Raynaud phenomenon, and positiveserologies for antinuclear, anticentromere, and anti-Saccharomyces cerevisiae antibodies.


Assuntos
Dermatoses Faciais/diagnóstico , Dermatoses do Pé/diagnóstico , Doença Granulomatosa Crônica/imunologia , Lúpus Eritematoso Cutâneo/diagnóstico , Anticorpos Antinucleares/imunologia , Anticorpos Antifúngicos/imunologia , Queilite/complicações , Queilite/diagnóstico , Queilite/imunologia , Criança , Dermatoses Faciais/complicações , Dermatoses Faciais/imunologia , Dermatoses Faciais/patologia , Dermatoses do Pé/complicações , Dermatoses do Pé/imunologia , Dermatoses do Pé/patologia , Doença Granulomatosa Crônica/complicações , Humanos , Lúpus Eritematoso Cutâneo/complicações , Lúpus Eritematoso Cutâneo/imunologia , Lúpus Eritematoso Cutâneo/patologia , Masculino , Úlceras Orais/complicações , Úlceras Orais/diagnóstico , Úlceras Orais/imunologia , Doença de Raynaud/complicações , Doença de Raynaud/diagnóstico , Doença de Raynaud/imunologia , Fatores de Risco , Saccharomyces cerevisiae/imunologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA