A novel oncogenic enhancer of estrogen receptor-positive breast cancer

Estrogen receptor-positive (ER+) breast cancer accounts for the majority of breast cancers diagnosed, and nearly 20% of patients do not respond to endocrine therapy. The pathogen-esis of ER+ breast cancer has not been well elucidated. The enhancer is a cis-regulatory element that promotes gene tran-scription and plays an important role in the spatiotemporal expression of cellular genes. Nevertheless, the oncogenic enhancer and its role in the occurrence and progression of cancer remain unclear. Here, we report a novel oncogenic enhancer (named aE,& bdquo;yc) for c-Myc and reveal its activation mechanism in ER+ breast cancer. The results demonstrated that aE,& bdquo;yc enhanced the transcription of downstream genes more than 20-fold. The deletion of the 7-bp region (GGT TGCA) in aE,& bdquo;yc significantly downregulated the expression of c-Myc, resulting in cell nuclear changes, cell-cycle arrest, cell apoptosis, and finally, remarkable inhibition of cell proliferation. In conclusion, the present study discovers a novel oncogenic enhancer aE,& bdquo;yc (801 base pairs [bp], at Chr8: 127668529-127669329) and offers a remarkable core enhancer target (GGTTGCA) of aE,& bdquo;yc for gene therapy of ER+ breast cancer.