%0 Journal Article
%T VEGF and KRAS are Potential Targets of miR-206 Modulation in Triple Negative Breast Cancer
%A Adel Nassar
%A Fawziya A.R. Ibrahim
%A Mohammad A. Ahmad
%A Mohammad M. Nasef
%A Nadia A. Abd El Moneim
%A Samia A. Ebeid
%A Sanaa Shawky
%A Shaymaa E. El Feky
%J Journal of Cancer Research and Treatment
%D 2019
%R 10.12691/jcrt-7-1-2
%X Triple negative is a subtype of breast cancer characterized by lack of expression of hormone receptors (ER, PR and Her2/neu). Due to the limited treatment options, the search for novel treatment targets continues. The aim of this study was to assess the differential expression of miR-206, VEGF and KRAS in TNBC and non-TNBC tissues and cell lines and to evaluate the modulatory effect of miR-206 on the key oncogenic targets VEGF and KRAS. The expression of miR-206, VEGF and KRAS was quantified using real time PCR in both paraffin embedded breast cancer and adjacent tissues as well as in MDA-MB-231 and MCF-7 cell lines. Cell lines were transfected with different concentrations of miR-206 mimic and their viability were assessed using MTT assay. Our results indicated that miR-206 was significantly downregulated in cancerous compared to non-cancerous tissues with a more pronounced downregulation in TNBC than non-TNBC tissues. VEGF and KRAS were significantly upregulated in TNBC compared to non-TNBC and their expression was negatively correlated to miR-206 expression. Transfection of TNBC and non-TNBC cell lines with miR-206 mimic resulted in a dose dependent reduction in cell viability as well as a significant reduction in VEGF and KRAS expression. In conclusion, based on our combined human tissues and cell line-based investigations we can suggest that VEGF and KRAS may be potential targets for miR-206-mediated regulation and that their targeting by miR-206 can be a highly efficient therapeutic strategy in TNBC
%U http://www.sciepub.com/JCRT/abstract/10701