Evaluation of the Expression Level and Hormone Receptor Association of miR-126 in Breast Cancer

13Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Rouigari, M., Dehbashi, M., Tabatabaeian, H., Ghaedi, K., Mohammadynejad, P., & Azadeh, M. (2019). Evaluation of the Expression Level and Hormone Receptor Association of miR-126 in Breast Cancer. Indian Journal of Clinical Biochemistry, 34(4), 451–457. https://doi.org/10.1007/s12291-018-0766-6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free