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<Emphasis Type="Italic">CDKN1A</Emphasis> histone acetylation and gene expression relationship in gastric adenocarcinomas
Authors:Fernanda Wisnieski  Danielle Queiroz Calcagno  Mariana Ferreira Leal  Leonardo Caires Santos  Carolina Oliveira Gigek  Elizabeth Suchi Chen  Sâmia Demachki  Ricardo Artigiani  Paulo Pimentel Assumpção  Laércio Gomes Lourenço  Rommel Rodríguez Burbano  Marília Cardoso Smith
Institution:1.Disciplina de Genética, Departamento de Morfologia e Genética,Universidade Federal de S?o Paulo,S?o Paulo,Brazil;2.Núcleo de Pesquisas em Oncologia, Hospital Jo?o de Barros Barreto,Universidade Federal do Pará,Belém,Brazil;3.Departamento de Ortopedia e Traumatologia,Universidade Federal de S?o Paulo,S?o Paulo,Brazil;4.Departamento de Patologia,Universidade Federal de S?o Paulo,S?o Paulo,Brazil;5.Disciplina de Gastroenterologia Cirúrgica, Departamento de Cirurgia,Universidade Federal de S?o Paulo,S?o Paulo,Brazil;6.Laboratório de Citogenética Humana, Instituto de Ciências Biológicas,Universidade Federal do Pará,Belém,Brazil
Abstract:CDKN1A is a tumor suppressor gene involved in gastric carcinogenesis and is a potential target for histone deacetylase inhibitor-based therapies. Upregulation of CDKN1A is generally observed in several cell lines after histone deacetylase inhibitor treatment; however, little is known about the histone acetylation status associated with this gene in clinical samples, including gastric tumor tissue samples. Therefore, our goal was to quantify the H3K9 and H4K16 acetylation levels associated with three CDKN1A regions in 21 matched pairs of gastric adenocarcinoma and corresponding adjacent non-tumor samples by chromatin immunoprecipitation and to correlate these data with the gene expression. Our results demonstrated that the ?402, ?20, and +182 CDKN1A regions showed a significantly increased acetylation level in at least one of the histones evaluated (p < 0.05, for all comparisons), and these levels were positively correlated in gastric tumors. However, an inverse correlation was detected between both H3K9 and H4K16 acetylation at the ?402 CDKN1A region and mRNA levels in gastric tumors (r = ?0.51, p = 0.02; r = ?0.60, p < 0.01, respectively). Furthermore, increased H4K16 acetylation at the ?20 CDKN1A region was associated with gastric tumors of patients without lymph node metastasis (p = 0.04). These results highlight the complexity of these processes in gastric adenocarcinoma and contribute to a better understanding of CDKN1A regulation in carcinogenesis.
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