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Residual expression of SMYD2 and SMYD3 is associated with the acquisition of complex karyotype in chronic lymphocytic leukemia.
Oliveira-Santos, Wilson; Rabello, Doralina Amaral; Lucena-Araujo, Antônio Roberto; de Oliveira, Fábio Morato; Rego, Eduardo Magalhaes; Pittella Silva, Fábio; Saldanha-Araujo, Felipe.
Afiliação
  • Oliveira-Santos W; Laboratory of Molecular Pathology of Cancer, Faculty of Health Sciences, University of Brasília, Av. L2 Norte, Brasília, DF, 70.910-900, Brazil.
  • Rabello DA; Laboratory of Molecular Pathology of Cancer, Faculty of Health Sciences, University of Brasília, Av. L2 Norte, Brasília, DF, 70.910-900, Brazil.
  • Lucena-Araujo AR; Department of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, SP, 14.048-900, Brazil.
  • de Oliveira FM; Department of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, SP, 14.048-900, Brazil.
  • Rego EM; Department of Internal Medicine, Medical School of Ribeirão Preto, University of São Paulo, Av. Bandeirantes 3900, Ribeirão Preto, SP, 14.048-900, Brazil.
  • Pittella Silva F; Laboratory of Molecular Pathology of Cancer, Faculty of Health Sciences, University of Brasília, Av. L2 Norte, Brasília, DF, 70.910-900, Brazil.
  • Saldanha-Araujo F; Laboratory of Molecular Pathology of Cancer, Faculty of Health Sciences, University of Brasília, Av. L2 Norte, Brasília, DF, 70.910-900, Brazil. felipearaujo@unb.br.
Tumour Biol ; 37(7): 9473-81, 2016 Jul.
Article em En | MEDLINE | ID: mdl-26790435
SET and MYND domain containing 2 (SMYD2) and the SET and MYND domain containing 3 (SMYD3) are the most studied and well-characterized members of SMYD family. It has been demonstrated that their altered expression is associated with the progression of several solid tumors. Nevertheless, whether these methyltransferases exert any impact in chronic lymphocytic leukemia (CLL) remains unknown. Here, we investigated the gene expression profile of SMYD2 and SMYD3 in 59 samples of CLL and 10 normal B cells. The obtained results were associated with white blood cells (WBC) and platelet counts, ZAP-70 protein expression, and cytogenetic analysis. We found that SMYD2 and SMYD3 are overexpressed in CLL patients and, interestingly, patients with residual expression of both genes presented a high WBC count and complex karyotype. Furthermore, a strong correlation between SMYD2 and SMYD3 gene expression was unveiled. Our data demonstrate the association of a residual expression of SMYD2 and SMYD3 with CLL progression indicators and suggests both genes are regulated by a common transcriptional control in this type of cancer. These results may provide the basis for the development of new therapeutic strategies to prevent CLL progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Aberrações Cromossômicas / Histona-Lisina N-Metiltransferase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Tumour Biol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais / Regulação Neoplásica da Expressão Gênica / Aberrações Cromossômicas / Histona-Lisina N-Metiltransferase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Tumour Biol Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Brasil