Canine distemper virus induces apoptosis in cervical tumor derived cell lines

Apoptosis can be induced or inhibited by viral proteins, it can form part of the host defense against virus infection, or it can be a mechanism for viral spread to neighboring cells. Canine distemper virus (CDV) induces apoptotic cells in lymphoid tissues and in the cerebellum of dogs naturally infected. CDV also produces a cytopathologic effect, leading to apoptosis in Vero cells in tissue culture. We tested canine distemper virus, a member of the Paramyxoviridae family, for the ability to trigger apoptosis in HeLa cells, derived from cervical cancer cells resistant to apoptosis. To study the effect of CDV infection in HeLa cells, we examined apoptotic markers 24 h post infection (pi), by flow cytometry assay for DNA fragmentation, real-time PCR assay for caspase-3 and caspase-8 mRNA expression, and by caspase-3 and -8 immunocytochemistry. Flow cytometry showed that DNA fragmentation was induced in HeLa cells infected by CDV, and immunocytochemistry revealed a significant increase in the levels of the cleaved active form of caspase-3 protein, but did not show any difference in expression of caspase-8, indicating an intrinsic apoptotic pathway. Confirming this observation, expression of caspase-3 mRNA was higher in CDV infected HeLa cells than control cells; however, there was no statistically significant change in caspase-8 mRNA expression profile. Our data suggest that canine distemper virus induced apoptosis in HeLa cells, triggering apoptosis by the intrinsic pathway, with no participation of the initiator caspase -8 from the extrinsic pathway. In conclusion, the cellular stress caused by CDV infection of HeLa cells, leading to apoptosis, can be used as a tool in future research for cervical cancer treatment and control

Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer

Abstract Gastric cancer (GC) is the fifth most common type of cancer worldwide with high incidences in Asia, Central, and South American countries. This patchy distribution means that GC studies are neglected by large research centers from developed countries. The need for further understanding of this complex disease, including the local importance of epidemiological factors and the rich ancestral admixture found in Brazil, stimulated the implementation of the GE4GAC project. GE4GAC aims to embrace epidemiological, clinical, molecular and microbiological data from Brazilian controls and patients with malignant and pre-malignant gastric disease. In this letter, we summarize the main goals of the project, including subject and sample accrual and current findings

Ecomorphology of Astyanax species in streams with different substrates

In the present study, we assessed the ecomorphology of two species of Astyanax in streams with different substrates found in the Rio São Francisco Basin. The dominant substrate of each stream was defined as either "fine" (0 to 2 mm), "gravel" (2 to 250 mm), "rock" (> 250 mm), or "leaf bank". We analyzed a total of 22 ecomorphological attributes of Astyanax intermedius Eigenmann, 1908 (127 individuals) and Astyanax rivularis (Lütken, 1875) (238 individuals) adults. We detected significant ecomorphological differences between the populations of A. rivularis and A. intermedius from habitats with different types of substrates. However, the two species did not show the same morphological differences depending on the type of substrate. These results confirmed the hypothesis that individuals from environments with different characteristics may have different ecomorphological patterns. Knowing that morphology is associated with habitat use and available resources, the loss of a resource or a modification in the environment may directly affect the permanence of a species, leading to a loss of morphologic diversity

RISK ANALYSIS OF ACETONE AND PHENOL PRODUCTION PROCESS FROM BENZENE AND PROPENE

Process safety is a main concern in chemical and petrochemical industries nowadays. In this context, an applied hazard identification and risk assessment were performed in a hypothetical acetone plant based on the Hock process. The capacity of the plant was chosen according to Brazilian market conditions. Quantitative risk analysis for a few scenarios was carried out by using PhastRisk® software. As a result, equipment and pipelines were designed to meet process throughput as well as safety requirements. Some hazard properties of process stream, such as flammability and toxicity, were evaluated and their impact was taken into account in the plant. Based on a qualitative risk analysis, some recommendations to reduce incident probability were proposed. The quantitative approach also indicated the critical zone of impact, the radiation emitted and the toxic cloud dispersion that would take place from the leakage point. The results showed that the worst case scenario involved a leakage of acetone and propylene

A Catalytically Inactive Lys49 PLA2 Isoform from Bothrops jararacussu venom that Stimulates Insulin Secretion in Pancreatic Beta Cells

A new secretory phospholipase A2 (sPLA2) isoform from Bothrops jararacussu venom (BjVIII) has been characterized by causing platelet aggregation, an absent activity in BthTx-I, Prtx-I and PrTx-II sPLA2s. According to our results, BjVIII also enhances insulin release by the pancreatic beta cells. The complete amino acid sequence of the new isoform was determined by Edman degradation and de novo peptide sequencing. These analyses showed a G35K amino acid modification for BjVIII in comparison with BthTx-I, PrTx-I and Prtx-II, a structural difference that has been related to the conflicting biological activities among BjVIII and other Lys49 sPLA2s. The whole set of evidences collected in this work indicates that, besides the C-terminal region and B-wing of PLA2, the calcium binding loop in BjVIII should be considered as an important region, involved in the pharmacological effects of Lys49-sPLA2 isoforms from the Bothrops genus.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq