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Liu Y, miR-206 Inhibits Laryngeal Carcinoma Cell Multiplication, Migration, and Invasion

Liu Y, Song Y, Chen X, Fan J, Zheng W, Cao C. miR-206 Inhibits Laryngeal Carcinoma Cell Multiplication, Migration, and Invasion. J Healthc Eng. 2021 Nov 26;2021:5614861. doi: 10.1155/2021/5614861. PMID: 34868522; PMCID: PMC8642001.

miR-206 Inhibits Laryngeal Carcinoma Cell Multiplication, Migration, and Invasion

Yiling Liu 1YunTao Song 1Xiaojuan Chen 2Junfang Fan 3Wei Zheng 4Chen Cao 5

Affiliations

  • 1Department of Otorhinolaryngology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 45000, China.

  • 2Department of Nursing, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 45000, China.

  • 3Department of Surgery, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 45000, China.

  • 4Dean's Office, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 45000, China.

  • 5Department of Intervention, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 45000, China.

Abstract

Laryngeal carcinoma (LC) is one of the common human cancer types. MicroRNAs (miRNAs) were reported to be the essential regulators in cancer diagnosis, treatment, and prognosis. It was reported that miR-206 expression was reduced in various neoplastic diseases. However, the role and functional mechanism of miR-206 in LC progression remain unclear. In this research, miR-206 was found to be associated with tumor-node-metastasis (TNM) staging. In addition, the area under the curve (AUC) of miR-206 was 0.902 for diagnosis of LC and 0.854 for differential diagnosis of stage I-II and stage III-IV patients. Low expression of miR-206 was associated with poor prognosis of LC patients. miR-206 expression was an independent factor affecting the prognosis of LC patients, as revealed by the Cox regression analysis. In vitro experiments demonstrated that miR-206 overexpression reduced cell multiplication, invasion, and migration and increased cell apoptosis in LC cells. Moreover, SOX9 was a target of miR-206, and miR-206 negatively regulated SOX9 expression. Collectively, miR-206 might be a promising biomarker with diagnostic and prognostic value for LC, and the miR-206/SOX9 axis might be a candidate target for LC therapy.

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