Clinicopathological features associated to miRNA-195 expression in patients with breast cancer: Evidence of a potential biomarker

18Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

Background & Objective: MiRNAs are a systematic class of small non-coding RNAs with impending role as tumor biomarkers. Our objective was to identify the level of expression of Mir-195 in patients with breast cancer along with its correlation with clinicopathologic features. Methods: A total of 209 females in which 139 histologically diagnosed breast cancer (BC) cases and 70 healthy controls matched for age, their relative clinical and histopathological findings were recorded from their laboratory reports and hospital record of the patients. Plasma was used for extraction of total RNA and cDNA was prepared by using both miR-195 stem loop RT primers and gene specific antisense primers while U6 IT was used as control. Quantitative real-time PCR (qRT-PCR) for miR-195 expression status was performed and amplification (down regulation) was recorded. Results: Of 139 samples the expression of miR-195 was down regulated in 72.6% cases and the remaining 27.3% cases behaved same as 70 healthy or normal controls. Significant correlation of low miR-195 expression with higher differentiation grade, lymph node metastasis and clinical stage was found. Conclusion: Significant correlation between miR-195 expression and some clinicopathological features were recognized. MiR-195 could be used as potential non-invasive, molecular biomarker for early detection of breast cancer.

Cite

CITATION STYLE

APA

Nadeem, F., Hanif, M., Ahmed, A., Jamal, Q., & Khan, A. (2017). Clinicopathological features associated to miRNA-195 expression in patients with breast cancer: Evidence of a potential biomarker. Pakistan Journal of Medical Sciences, 33(5), 1242–1247. https://doi.org/10.12669/pjms.335.13008

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