Your browser doesn't support javascript.
loading
Differential expression of miR-143, miR-145 and miR-150 in colorectal cancer
Torres, Natalia; Amaral, Fernando Colbari; Oliveira, Eduardo Borges; Saggioro, Fabiano Pinto; Rocha, José Ribeiro; Feres, Omar; Silva Júnior, Wilson Araujo; Oliveira, Ricardo Brandt; Castro, Margaret.
  • Torres, Natalia; Hospital Albert Eintein. São Paulo. BR
  • Amaral, Fernando Colbari; Hospital Albert Eintein. São Paulo. BR
  • Oliveira, Eduardo Borges; Hospital Albert Eintein. São Paulo. BR
  • Saggioro, Fabiano Pinto; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Anatomia Cirurgica. Ribeirão Preto. BR
  • Rocha, José Ribeiro; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Anatomia Cirurgica. Ribeirão Preto. BR
  • Feres, Omar; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Anatomia Cirurgica. Ribeirão Preto. BR
  • Silva Júnior, Wilson Araujo; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Genética. Ribeirão Preto. BR
  • Oliveira, Ricardo Brandt; Hospital Albert Eintein. São Paulo. BR
  • Castro, Margaret; Hospital Albert Eintein. São Paulo. BR
Appl. cancer res ; 31(4): 116-121, 2011.
Article in English | LILACS, Inca | ID: lil-655864
ABSTRACT
Background: Recent reports indicated the involvement of microRNAs (miRNAs) deregulation in colorectal adenomatous mucosa and different stages of colorectal cancer (CRC). Aims: The purpose of this study was to analyze a panel of miRNAs previously selected by bioinformatics analysis from SAGE human colorectal cancer library compared to normal colorectal library in order to identify microRNA species with altered expression in colorectal cancer. Methods: We analyzed the expression of let-7a, miR-21, miR-15a, miR-141, miR-143, miR-145 and miR-150 in 15 tumor tissues from patients who undergone surgery for CRC and 4 non-tumor adjacent tissues. The expression of miRNAs was measured by real-time PCR. Relative quantification of miRNA expression was calculated using the 2(-Delta Delta C(T)) method. Results: Our findings showed under expression of miR-143, miR-150 and miR-145 in about 6-fold (p = 0.05), 5-fold and 4-fold (p = 0.01), respectively, in CRC compared to normal colorectal tissue. In addition, there was no association between each miRNA expression and tumor stage or tumor localization. Conclusion: Our results support that under expression of miR-143, miR-150 and miR-145 might be involved in colorectal carcinogenesis. However, the lack of knowledge about miRNA target genes postpones full understanding of the biological functions of downregulated miRNAs in CRC.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Colorectal Neoplasms / Gene Expression / Gene Expression Regulation, Bacterial / MicroRNAs Type of study: Prognostic study Limits: Humans Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2011 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital Albert Eintein/BR / Universidade de São Paulo/BR

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: LILACS (Americas) Main subject: Colorectal Neoplasms / Gene Expression / Gene Expression Regulation, Bacterial / MicroRNAs Type of study: Prognostic study Limits: Humans Language: English Journal: Appl. cancer res Journal subject: Neoplasms Year: 2011 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital Albert Eintein/BR / Universidade de São Paulo/BR