Breast cancer is the most common malignant cancer among women. Both drug resistance
and metastasis are major problems in the treatment of breast cancer. Therefore, adjuvant therapy may improve
patients’ survival and affect their quality of life. It is suggested that epigallocatechin gallate (EGCG)
which is well known for its chemopreventive activity and acts on numerous molecular targets may inhibit
the growth and metastasis of some cancers. Hence, discovering the metastatic molecular mechanisms for
breast cancer may be useful for therapy.The aim of the study was to determine the effect of EGGC on the mRNA expression level of
genes such as ZEB1, ABCB1, MDM2, TWIST1 and PTEN in MCF-7 breast cancer cells.
MCF7/DOX were cultured in the presence of 0.2 μM DOX and EGCG (20-50 μM). The mRNA
expression level was determined by real-time quantitative PCR using RealTime ready Custom Panel 96 kit.
Our results showed an important increase (about 2-fold for 20 μM EGCG + 0.2 μM DOX and
2.5-fold for 50 μM EGCG + 0.2 μM DOX, p<0.05) in ZEB1 expression levels. In case of ABCB1 gene lack
of influence on the mRNA level was observed (p>0.05). We also observed significant decrease of ZEB1
expression in MCF7 cells with 20 μM and 50 μM EGCG (p<0.05). In addition, EGCG (20 μM) caused an
increase of MDM2 and PTEN mRNA levels in almost 100% (p<0.05) and 40% (p>0.05), respectively. Lack
of the influence of EGCG was noted for the TWIST1 gene expression. In case of MCF7/DOX we showed an
increase of mRNA level of PTEN gene about 50% (p<0.05).
These results suggest that EGCG may be potentially used in adjuvant therapy in the breast
cancer treatment.
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