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Navegando por Assunto "CDH1"

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    Avaliação do perfil de metilação e expressão do gene CDH1 em Cebus apella como modelo experimental para câncer gástrico
    (Universidade Federal do Pará, 2012-07-09) ANTUNES, Symara Rodrigues; BORGES, Barbara do Nascimento; http://lattes.cnpq.br/0676220027193876; ANSELMO, Nilson Praia; http://lattes.cnpq.br/6518287721873199
    The gastric cancer remains a major cause of death among cancers in the world. In Brazil, are expected around 500 000 new cases in 2012/2013. The origin of stomach cancer, as in others, arises from the accumulation of genetic alterations. Therefore, it is necessary to know which genetic changes are important in triggering the pathogenesis of gastric cancer. We know that the intestinal type develops through well defined stages. The MNU - a known carcinogen - when ingested in oral form at dosages determined triggers development of this histological type of gastric cancer. Based on this knowledge, we conducted an experiment with six specime of Cebus paella, induced to develop intestinal type gastric cancer. The animals consumed 16mg/kg of body weight daily drugs. All pre-neoplasic lesions developed. Due to drug toxicity, only one survived the entire treatment and developed a tumor. Periodic evaluations were made of animals in pre-determined days (the beginning, days 120, 150, 300, 940) during which samples were made of the gastric mucosa. We collected 20 samples of tissue, distributed among normal mucosa, gastritis, dysplasia, metaplasia, and tumor. DNA extracted from these samples for further analyzes of the CDH1 gene. There is no sequence of this gene in the literature for the species under study. So the first step was to get this sequence. Using the initiators constructed from sequences of CDH1 Callithrix jacchus (species phylogenetically closer to C. apella) we get a sequence of 342pb. There is a similarity of 98% with humans, the presence of binding sites for transcription factors like (sp1, Ap2, NF-x, AREB6, Puf and CTF) and the presence of CAAT Box. The sequence has 30 CpG sites could suffer epigenetic regulation. We also performed MSP analysis with specific primers and found that the region analyzed, there was predominance of the unmethylated CDH1 alleles for all samples pre-neoplastic and adenocarcinoma sample is methylated. When we compared these data with immunohistochemistry revealed that only tumor sample did not express the protein cadherin. Our analyzes suggest that methylation of the CDH1 gene plays an important role in gastric tumorigenesis in C. apella. And, from the similarity between sequences, we suggest that the same occurs in humans. This cadherin promoter methylation leads to inactivation of the gene and establishment of gastric adenocarcinomas. The cadherin promoter hypermethylation has been reported in several articles associated with the development of gastric cancer.
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    CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS)
    (Universidade Federal do Pará, 2016-06) EL HUSNY, Antonette Souto; MORAES, Milene Raiol de; AMADOR, Marcos Antônio Trindade; SANTOS, André Maurício Ribeiro dos; MONTAGNINI, Andre Luis; BARBOSA, Maria Silvanira Ribeiro; SILVA, Artur Luiz da Costa da; ASSUMPÇÃO, Paulo Pimentel de; ISHAK, Geraldo; SANTOS, Sidney Emanuel Batista dos; PINTO, Pablo Diego do Carmo; CRUZ, Aline Maria Pereira; SANTOS, Ândrea Kely Campos Ribeiro dos
    Gastric cancer is considered to be the fifth highest incident tumor worldwide and the third leading cause of cancer deaths. Developing regions report a higher number of sporadic cases, but there are only a few local studies related to hereditary cases of gastric cancer in Brazil to confirm this fact. CDH1 germline mutations have been described both in familial and sporadic cases, but there is only one recent molecular description of individuals from Brazil. In this study we performed Next Generation Sequencing (NGS) to assess CDH1 germline mutations in individuals who match the clinical criteria for Hereditary Diffuse Gastric Cancer (HDGC), or who exhibit very early diagnosis of gastric cancer. Among five probands we detected CDH1 germline mutations in two cases (40%). The mutation c.1023T > G was found in a HDGC family and the mutation c.1849G > A, which is nearly exclusive to African populations, was found in an early-onset case of gastric adenocarcinoma. The mutations described highlight the existence of gastric cancer cases caused by CDH1 germline mutations in northern Brazil, although such information is frequently ignored due to the existence of a large number of environmental factors locally. Our report represent the first CDH1 mutations in HDGC described from Brazil by an NGS platform.
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