Eur Rev Med Pharmacol Sci 2018; 22 (14): 4564-4572
DOI: 10.26355/eurrev_201807_15512

Effect of miR-363 on the proliferation, invasion and apoptosis of laryngeal cancer by targeting Mcl-1

W.-T. Feng, R. Yao, L.-J. Xu, X.-M. Zhong, H. Liu, Y. Sun, L.-L. Zhou

Department of Oncology, The Affiliated Huai’an No. 1 People’s Hospital of Nanjing Medical University, Huai’an, China. bogy2004a@163.com


OBJECTIVE: To investigate the potential effect of miR-363 on the development of laryngeal cancer and to reveal the relevant mechanism.

PATIENTS AND METHODS: The expression level of miR-363 was detected in laryngeal cancer tissues and cells (TU-177), respectively. Luciferase assay was performed to evaluate the interaction between miR-363 and myeloid cell leukemia-1 (Mcl-1). The effect of the miR-363/Mcl-1 axis on TU-177 cells was determined by subsequent experiments including cell proliferation, invasion, apoptosis and the expression level of Mcl-1.

RESULTS: In the present study, we found that miR-363 was both repressed in laryngeal cancer tissues and cells (TU-177). To find the regulating target of miR-363, we searched three publicly available algorithms, including TargetScan, miRDB, and microRNA. Results showed that Mcl-1 was a direct target of miR-363, and the Luciferase assay confirmed our suggestion. Subsequent experiments indicated that the decreased expression of Mcl-1 resulting from the up-regulation of miR-363 could deaccelerate cell proliferation and invasion, and accelerate cell apoptosis in laryngeal cancer cells.

CONCLUSIONS: Our research revealed the suppressed function of miR-363 in laryngeal cancer by targeting Mcl-1. Meanwhile, we found that the restoration of miR-363 could serve as a potential therapeutic strategy for the treatment of laryngeal cancer.

Free PDF Download

To cite this article

W.-T. Feng, R. Yao, L.-J. Xu, X.-M. Zhong, H. Liu, Y. Sun, L.-L. Zhou
Effect of miR-363 on the proliferation, invasion and apoptosis of laryngeal cancer by targeting Mcl-1

Eur Rev Med Pharmacol Sci
Year: 2018
Vol. 22 - N. 14
Pages: 4564-4572
DOI: 10.26355/eurrev_201807_15512