A high-density association screen of 155 ion transport genes for involvement with common migraine

The clinical overlap between monogenic Familial Hemiplegic Migraine (FHM) and common migraine subtypes, and the fact that all three FHM genes are involved in the transport of ions, suggest that ion transport genes may underlie susceptibility to common forms of migraine. To test this leading hypothesis, we examined common variation in 155 ion transport genes using 5257 single nucleotide polymorphisms (SNPs) in a Finnish sample of 841 unrelated migraine with aura cases and 884 unrelated non-migraine controls. The top signals were then tested for replication in four independent migraine case-control samples from the Netherlands, Germany and Australia, totalling 2835 unrelated migraine cases and 2740 unrelated controls. SNPs within 12 genes (KCNB2, KCNQ3, CLIC5, ATP2C2, CACNA1E, CACNB2, KCNE2, KCNK12, KCNK2, KCNS3, SCN5A and SCN9A) with promising nominal association (0.00041 < P < 0.005) in the Finnish sample were selected for replication. Although no variant remained significant after adjusting for multiple testing nor produced consistent evidence for association across all cohorts, a significant epistatic interaction between KCNB2 SNP rs1431656 (chromosome 8q13.3) and CACNB2 SNP rs7076100 (chromosome 10p12.33) (pointwise P = 0.00002; global P = 0.02) was observed in the Finnish case-control sample. We conclude that common variants of moderate effect size in ion transport genes do not play a major role in susceptibility to common migraine within these European populations, although there is some evidence for epistatic interaction between potassium and calcium channel genes, KCNB2 and CACNB2. Multiple rare variants or trans-regulatory elements of these genes are not ruled out.

MicroRNA-155 Is Required for Mycobacterium bovis BCG-Mediated Apoptosis of Macrophages

Pathogenic rnycobacteria, including Mycobacterium tuberculosis and Mycobacterium bovis, cause significant morbidity and mortality worldwide. However, the vaccine strain Mycobacterium bovis BCG, unlike virulent strains, triggers extensive apoptosis of infected macrophages, a step necessary for the elicitation of robust protective immunity. We here demonstrate that M. bovis BCG triggers Toll-like receptor 2 (TLR2)-dependent microRNA-155 (miR-155) expression, which involves signaling cross talk among phosphatidylinositol 3-kinase (PI3K), protein kinase C delta (PKC delta), and mitogen-activated protein kinases (MAPKs) and recruitment of NF-kappa B and c-ETS to miR-155 promoter. Genetic and signaling perturbations presented the evidence that miR-155 regulates PKA signaling by directly targeting a negative regulator of PKA, protein kinase inhibitor alpha (PKI-alpha). Enhanced activation of PKA signaling resulted in the generation of PKA C-alpha; phosphorylation of MSK1, cyclic AMP response element binding protein (CREB), and histone H3; and recruitment of phospho-CREB to the apoptotic gene promoters. The miR-155-triggered activation of caspase-3, BAK1, and cytochrome c translocation involved signaling integration of MAPKs and epigenetic or posttranslational modification of histones or CREB. Importantly, M. bovis BCG infection-induced apoptosis was severely compromised in macrophages derived from miR-155 knockout mice. Gain-of-function and loss-of-function studies validated the requirement of miR-155 for M. bovis BCG's ability to trigger apoptosis. Overall, M. bovis BCG-driven miR-155 dictates cell fate decisions of infected macrophages, strongly implicating a novel role for miR-155 in orchestrating cellular reprogramming during immune responses to mycobacterial infection.

Oncogenic MicroRNA-155 Down-regulates Tumor Suppressor CDC73 and Promotes Oral Squamous Cell Carcinoma Cell Proliferation IMPLICATIONS FOR CANCER THERAPEUTICS

The CDC73 gene is mutationally inactivated in hereditary and sporadic parathyroid tumors. It negatively regulates beta-catenin, cyclin D1, and c-MYC. Down-regulation of CDC73 has been reported in breast, renal, and gastric carcinomas. However, the reports regarding the role of CDC73 in oral squamous cell carcinoma (OSCC) are lacking. In this study we show that CDC73 is down-regulated in a majority of OSCC samples. We further show that oncogenic microRNA-155 (miR-155) negatively regulates CDC73 expression. Our experiments show that the dramatic up-regulation of miR-155 is an exclusive mechanism for down-regulation of CDC73 in a panel of human cell lines and a subset of OSCC patient samples in the absence of loss of heterozygosity, mutations, and promoter methylation. Ectopic expression of miR-155 in HEK293 cells dramatically reduced CDC73 levels, enhanced cell viability, and decreased apoptosis. Conversely, the delivery of a miR-155 antagonist (antagomir-155) to KB cells overexpressing miR-155 resulted in increased CDC73 levels, decreased cell viability, increased apoptosis, and marked regression of xenografts in nude mice. Cotransfection of miR-155 with CDC73 in HEK293 cells abrogated its pro-oncogenic effect. Reduced cell proliferation and increased apoptosis of KB cells were dependent on the presence or absence of the 3'-UTR in CDC73. In summary, knockdown of CDC73 expression due to overexpression of miR-155 not only adds a novelty to the list of mechanisms responsible for its down-regulation in different tumors, but the restoration of CDC73 levels by the use of antagomir-155 may also have an important role in therapeutic intervention of cancers, including OSCC.

Sapientia, 1985, Vol. XL, nº 155 (número completo)

Contenido: La verdad (I). La verdad en sí misma y en las cosas / Octavio N. Derisi -- Carácter racional de la libertad / Octavio N. Derisi -- Libertad política : liberalismo y tomismo / Héctor H. Hernández -- Hilemorfismo y corporalidad / J. E. Bolzán -- Fenomenología de la sensación / Gabriel Chalmeta -- La teoría relacional de la personalidad según J. Nuttin / William R. Darós -- Notas y comentarios -- Bibliografía

Diário da Constituinte [gravação de vídeo] : [programa n. 155]

Técnicos em reforma sanitária, representantes da Assembleia Nacional Constituinte (ANC) e o Ministro da Saúde, Sr. Roberto Santos, reuniram-se para debater o tema: a saúde e a Constituinte. Segundo o ministro Roberto Santos o projeto de Constituição atual é um avanço quando coloca a saúde como um direito do cidadão e dever do Estado. A questão da saúde faz parte do título geral do projeto de Constituição, que trata da ordem social. No Artigo 350 fica determinado que o Estado deve criar políticas para eliminar ou reduzir o risco de doenças e garantir o acesso universal e gratuito à saúde. O Deputado José Elias Murad (PTB-MG) esclarece que este princípio significa que, em qualquer parte do país, qualquer brasileiro terá direito ao atendimento médico gratuito. O Deputado Arnaldo Faria de Sá (PTB-SP) vai apresentar um projeto de decisão para colocar já em votação a duração do mandato do Presidente José Sarney. Segundo ele, é necessário votar logo esse tema para que a Constituinte possa trabalhar em paz. Segundo o Regimento da Comissão de Sistematização, um projeto de decisão é todo assunto que precisa ser discutido quando surgir uma ameaça aos trabalhos da Constituinte. O Deputado Nilson Gibson (PMDB-PE) declara que a questão do mandato do presidente como um fato jurídico constituído, um direito adquirido. O Deputado Adolfo Oliveira (PL-RJ) afirma que é preciso caminhar para uma Constituição nova, com tudo reformado, tudo revisado e votação direta para todos os cargos eletivos. O Deputado Augusto Carvalho (PCB-DF), em nome do partido, apoia as eleições diretas para presidente da república em 1988. O Deputado Virgildásio Sena (PMDB-BA) afirma que não é a hora de decidir o mandato do presidente, já que ainda não se decidiu nem o sistema de governo. O Deputado Euclides Scalco (PMDB-PR) entende que é o momento de discutir na Comissão de Sistematização a questão do mandato do presidente e do regime de governo. O Deputado Ulysses Guimarães (PMDB-SP) entende que o Plenário é o fórum próprio para discutir o mandato e o sistema de governo, quando for votado o substitutivo.