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Evaluation of the Expression Level and Hormone Receptor Association of miR-126 in Breast Cancer.
Rouigari, Maedeh; Dehbashi, Moein; Tabatabaeian, Hossein; Ghaedi, Kamran; Mohammadynejad, Parisa; Azadeh, Mansoureh.
Afiliação
  • Rouigari M; Department of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
  • Dehbashi M; 2Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
  • Tabatabaeian H; 2Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
  • Ghaedi K; 3Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117545 Singapore.
  • Mohammadynejad P; 4Division of Cellular and Molecular Biology, Department of Biology, Faculty of Sciences, University of Isfahan, Hezar Jerib Ave., Azadi Sq., Isfahan, 81746-73441 Iran.
  • Azadeh M; 5Department of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Indian J Clin Biochem ; 34(4): 451-457, 2019 Oct.
Article em En | MEDLINE | ID: mdl-31686732
ABSTRACT
Breast cancer is a major cause of cancer-related death in women worldwide. miRNAs are new players of breast tumorigenesis, used as diagnostic and prognostic biomarkers. Among various miRNAs, miR-126 has been proposed to have a tumor suppressive role in HER2 positive cancer. However, to have a better understanding of its role, further validation is required. The aim of this study was evaluating miR-126 expression level in breast cancer tissues and investigating its potential association with HER2, estrogen and progesterone receptors. miR-126 expression level was measured in 108 specimens including 78 malignant and 30 normal samples using RT-qPCR. The outcome was statistically analyzed. In silico studies were performed to find the potential mechanism of action, through which miR-126 imposes its function. Down-regulation of miR-126 was observed in tumor samples, as compared to the matched normal tissues. Down-regulation of miR-126 was also associated significantly with the absence of estrogen receptor in malignant samples. No association between miR-126 expression and HER2 status was observed. Our in silico analyses showed the possible role of Crk, PI3K and Ras proto-oncogenes in breast cancer tumorigenesis. miR-126 is significantly down-regulated in breast cancer tissues. Statistically, it showed no correlation with HER2 positivity. However, the association between lower miR-126 and estrogen receptor negativity was observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Indian J Clin Biochem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Indian J Clin Biochem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Irã