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2.
Psychosom Med ; 78(7): 835-40, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27136503

RESUMO

OBJECTIVE: The Trier Social Stress Test (TSST) is one of the most widely used laboratory-based acute psychosocial stressors. However, there may be advantages to conducting the TSST through the virtual world, including reducing the cost and burden (i.e., no need for colocation between the evaluators and participants). The virtual TSST might also increase the standardization between studies and provide the capacity to bring psychology experiments to more settings (e.g., the home, the magnetic resonance imaging scanner). METHODS: Fifty undergraduate students participated in the TSST conducted through an online virtual reality program, using a computer screen and microphone/earphone headset. RESULTS: The present study found that the virtual TSST produced a significant acute stress response, measured both through cortisol (F(1,128) = 31.91, p < .001) and subjective report (F(1,148) = 72.86, p < .001). In addition, this method differentially produced a dampened cortisol response (F(1,126) = 4.41, p < .04) in those who had experienced recent loss (e.g., bereavement, romantic breakup, homesickness), similar to prior research. CONCLUSIONS: Virtual reality-based administration of the TSST and other mental challenge protocols increases the possibilities of many standard psychological experiments relevant to biobehavioral research.


Assuntos
Benchmarking/métodos , Hidrocortisona/metabolismo , Testes Neuropsicológicos/normas , Estresse Psicológico/diagnóstico , Interface Usuário-Computador , Adolescente , Adulto , Feminino , Humanos , Masculino , Reprodutibilidade dos Testes , Saliva , Estresse Psicológico/metabolismo , Adulto Jovem
3.
PLoS One ; 9(8): e104367, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25093503

RESUMO

We aimed to study the selective pressures interacting on SLC45A2 to investigate the interplay between selection and susceptibility to disease. Thus, we enrolled 500 volunteers from a geographically limited population (Basques from the North of Spain) and by resequencing the whole coding region and intron 5 of the 34 most and the 34 least pigmented individuals according to the reflectance distribution, we observed that the polymorphism Leu374Phe (L374F, rs16891982) was statistically associated with skin color variability within this sample. In particular, allele 374F was significantly more frequent among the individuals with lighter skin. Further genotyping an independent set of 558 individuals of a geographically wider population with known ancestry in the Spanish population also revealed that the frequency of L374F was significantly correlated with the incident UV radiation intensity. Selection tests suggest that allele 374F is being positively selected in South Europeans, thus indicating that depigmentation is an adaptive process. Interestingly, by genotyping 119 melanoma samples, we show that this variant is also associated with an increased susceptibility to melanoma in our populations. The ultimate driving force for this adaptation is unknown, but it is compatible with the vitamin D hypothesis. This shows that molecular evolution analysis can be used as a useful technology to predict phenotypic and biomedical consequences in humans.


Assuntos
Alelos , Antígenos de Neoplasias/genética , Predisposição Genética para Doença , Melanoma/genética , Proteínas de Membrana Transportadoras/genética , Seleção Genética , População Branca/genética , Europa (Continente) , Frequência do Gene , Interação Gene-Ambiente , Haplótipos , Humanos , Fases de Leitura Aberta , Polimorfismo de Nucleotídeo Único , Característica Quantitativa Herdável , Análise de Sequência de DNA , Espanha
4.
PLoS One ; 9(4): e95522, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24743186

RESUMO

Single nucleotide-polymorphisms (SNPs) are a source of diversity among human population, which may be responsible for the different individual susceptibility to diseases and/or response to drugs, among other phenotypic traits. Several low penetrance susceptibility genes associated with malignant melanoma (MM) have been described, including genes related to pigmentation, DNA damage repair and oxidative stress pathways. In the present work, we conducted a candidate gene association study based on proteins and genes whose expression we had detected altered in melanoma cell lines as compared to normal melanocytes. The result was the selection of 88 loci and 384 SNPs, of which 314 fulfilled our quality criteria for a case-control association study. The SNP rs6854854 in ANXA5 was statistically significant after conservative Bonferroni correction when 464 melanoma patients and 400 controls were analyzed in a discovery Phase I. However, this finding could not be replicated in the validation phase, perhaps because the minor allele frequency of SNP rs6854854 varies depending on the geographical region considered. Additionally, a second SNP (rs6431588) located on ILKAP was found to be associated with melanoma after considering a combined set of 1,883 MM cases and 1,358 disease-free controls. The OR was 1.29 (95% CI 1.12-1.48; p-value = 4×10-4). Both SNPs, rs6854854 in ANXA5 and rs6431588 in ILKAP, show population structure, which, assuming that the Spanish population is not significantly structured, suggests a role of these loci on a specific genetic adaptation to different environmental conditions. Furthermore, the biological relevance of these genes in MM is supported by in vitro experiments, which show a decrease in the transcription levels of ANXA5 and ILKAP in melanoma cells compared to normal melanocytes.


Assuntos
Anexina A5/genética , Melanoma/genética , Fosfoproteínas Fosfatases/genética , Estudos de Casos e Controles , Linhagem Celular Tumoral , Frequência do Gene/genética , Predisposição Genética para Doença/genética , Genótipo , Humanos , Polimorfismo de Nucleotídeo Único/genética
5.
Apoptosis ; 16(12): 1253-67, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21861192

RESUMO

Previously we found that terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca(2+) homeostasis. In this report, focusing our attention on the apoptotic mechanisms activated by terfenadine, we show that this drug can potentially activate distinct intrinsic signaling pathways depending on culture conditions. Serum-deprived conditions enhance the cytotoxic effect of terfenadine and caspase-4 and -2 are activated upstream of caspase-9. Moreover, although we found an increase in ROS levels, the apoptosis was ROS independent. Conversely, terfenadine treatment in complete medium induced ROS-dependent apoptosis. Caspase-4, -2, and -9 were simultaneously activated and p73 and Noxa induction were involved. ROS inhibition prevented p73 and Noxa expression but not p53 and p21 expression, suggesting a role for Noxa in p53-independent apoptosis in melanoma cells. Finally, we found that terfenadine induced autophagy, that can promote apoptosis. These findings demonstrate the great potential of terfenadine to kill melanoma cells through different cellular signaling pathways and could contribute to define new therapeutic strategies in melanoma.


Assuntos
Apoptose/efeitos dos fármacos , Autofagia/efeitos dos fármacos , Melanoma/fisiopatologia , Espécies Reativas de Oxigênio/metabolismo , Terfenadina/farmacologia , Caspases/metabolismo , Linhagem Celular Tumoral , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Humanos , Melanoma/genética , Melanoma/metabolismo , Transdução de Sinais/efeitos dos fármacos
6.
Hum Hered ; 69(1): 34-44, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-19797907

RESUMO

BACKGROUND/AIM: TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53. METHODS: We have analyzed the HapMap data for evidence of selection using F(ST) pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans. RESULTS: Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease. CONCLUSIONS: Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function.


Assuntos
Variação Genética , Proteínas/genética , Seleção Genética , Proteína Supressora de Tumor p53/genética , Alelos , Povo Asiático/genética , População Negra/genética , Frequência do Gene , Predisposição Genética para Doença/etnologia , Predisposição Genética para Doença/genética , Genótipo , Haplótipos , Humanos , Melanoma/etnologia , Melanoma/genética , Chaperonas Moleculares , Mutação , Havaiano Nativo ou Outro Ilhéu do Pacífico/genética , Polimorfismo de Nucleotídeo Único , Telomerase , População Branca/genética
7.
La Paz; 2001. 212 p. ^cuadros y anexos.
Tese em Espanhol | LIBOCS, LIBOSP | ID: biblio-1312020

RESUMO

El objetivo fundamental, consiste en la aplicacion del enfoque de analisis y diseño de sistemas para desarrollar e implementar un Sistema de Informacion para la "Cooperativa de Agua Potable Ovejuyo Ltda". Como campo de aplicacion, el trabajo esta dirigido a la aplicacion en una organizacion que presta servicios de abastecimiento de agua. Tomando como area de trabajo el control de las actividades que le permiten a la organizacion captar recursos financieros de sus socios, para permitir su normal funcionamiento y desarrollo. Por las caracteristicas de este tipo de proyectos, se ha logrado realizar un trabajo netamente practico, permitiendo la utilizacion de las bondades que brindan las herramientas de ultima generacion en el aspecto informatico.

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