Citation
- Authors: Derouet, M. F., Dakpo, E., Wu, L., Zehong, G., Conner, J., Keshavjee, S., de Perrot, M., Waddell, T., Elimova, E., Yeung, J., Darling, G. E.
- Year: 2018
- Journal: Oncotarget 9
- Applications: in vitro / siRNA / jetPRIME
- Cell type: SK-GT-4
Abstract
Adenocarcinoma of the esophagus is increasing in frequency and is the 6th most common cause of cancer death in North America. In adenocarcinoma cell lines, we have previously demonstrated that expression of miR-145, leads to enhanced invasion, resistance to anoikis and better attachment to fibronectin in esophageal adenocarcinoma. In contrast, expression of miR-145 acts as a tumor suppressor in squamous cell carcinoma. The molecular mechanisms responsible for the oncogenic effects of miR-145 were investigated. In this report, we demonstrate that we can partially recreate the miR-145 effects in EAC by knock down of the expression of c-Myc, which is one of the targets of miR-145. Knocking down of c-Myc expression resulted in upregulation of integrin subunits