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SIVA, a target of p53, is downregulated in myelodysplastic syndromes
Machado-Neto, João Agostinho; Campos, Paula de Melo; Favaro, Patricia; Lazarini, Mariana; Scopim-Ribeiro, Renata; Lorand-Metze, Irene; Costa, Fernando Ferreira; Saad, Sara Terezinha Olalla; Traina, Fabiola.
  • Machado-Neto, João Agostinho; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Campos, Paula de Melo; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Favaro, Patricia; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Lazarini, Mariana; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Scopim-Ribeiro, Renata; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Lorand-Metze, Irene; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Costa, Fernando Ferreira; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Saad, Sara Terezinha Olalla; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
  • Traina, Fabiola; University of Campinas, Hemocentro-Unicamp. Instituto Nacional de Ciência e Tecnologia do Sangue. Hematology and Hemotherapy Center. Campinas. BR
Appl. cancer res ; 37: 1-7, 2017. tab, ilus
Article in English | LILACS, Inca | ID: biblio-915402
ABSTRACT

Background:

SIVA is a transcriptional target of p53 that plays a potential role in the development and progression of cancer. In this study, we analyzed SIVA1 and SIVA2 expression, and its association with clinical features and TP53 and MDM2 expression in bone marrow cells from healthy donors and myelodysplastic syndrome (MDS) patients.

Methods:

Fifty-five untreated patients with MDS and 22 healthy donors were included. Gene expression was evaluated by quantitative PCR. For statistical analysis, Mann­Whitney test, Spearman correlation analysis and Log-rank (Mantel-Cox) were used, as appropriate. A p value <0.05 was considered statistically significant.

Results:

SIVA1 and SIVA2 transcripts were significantly decreased in bone marrow samples from MDS patients compared to healthy donors, and positively correlated with MDM2 and TP53 expression in MDS patients (all p < 0.05). MDM2 expression was also downregulated in bone marrow samples from MDS patients compared to healthy donors (p < 0.05). However, SIVA1, SIVA2, MDM2 and TP53 expressions did not impact on MDS outcomes.

Conclusions:

SIVA1 and SIVA2 transcripts are downregulated in bone marrow samples from MDS patients (AU)
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Myelodysplastic Syndromes / Genes, p53 / Apoptosis Inducing Factor Limits: Adult / Female / Humans / Male Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: University of Campinas, Hemocentro-Unicamp/BR

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Full text: Available Index: LILACS (Americas) Main subject: Myelodysplastic Syndromes / Genes, p53 / Apoptosis Inducing Factor Limits: Adult / Female / Humans / Male Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: University of Campinas, Hemocentro-Unicamp/BR