| Literature DB >> 30569106 |
Lai-Sheung Chan1, On-Ying Man1, Hoi-Hin Kwok1, Luo Chen1, King-Chi Chan1, Hong-Lok Lung1, Roger Kai-Cheong Ngan2, Ricky Ngok-Shun Wong1, Kwok-Wai Lo3, Anne Wing-Mui Lee2, George Sai-Wah Tsao2, Michael Kahn4, Maria Li Lung2, Nai-Ki Mak1.
Abstract
The Wnt signaling pathway is known to serve an important role in the control of cell migration. The present study analyzed the mechanisms underlying the in vitro modulation of the migration of nasopharyngeal carcinoma (NPC) cells by the CREB‑binding protein/catenin antagonist and Wnt modulator ICG‑001. The results revealed that ICG‑001‑mediated inhibition of tumor cell migration involved downregulated mRNA and protein expression of the Wnt target gene cluster of differentiation (CD)44. It was also demonstrated that ICG‑001 downregulated the expression of CD44, and this effect was accompanied by restored expression of microRNA (miRNA)‑150 in various NPC cell lines. Using a CD44 3'‑untranslated region luciferase reporter assay, miR‑150 was confirmed to be a novel CD44‑targeting miRNA, which could directly target CD44 and subsequently regulate the migration of NPC cells. The present study provides further insight into the inhibition of tumor cell migration through the modulation of miRNA expression by the Wnt modulator ICG‑001.Entities:
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Year: 2018 PMID: 30569106 DOI: 10.3892/ijo.2018.4664
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650