Yan Wang,
Hui Ren,
Qing Wang,
Shuang Li,
Yanhua Lu,
Wei Masu,
Juan Zhang,
Tao Wang
The Second Central Hospital Dental Baoding City, Hebei Province, 072750, China;
For correspondence:- Tao Wang
Email: vfj89895@126.com Tel:+8617764436922
Accepted: 10 August 2021
Published: 30 December 2021
Citation:
Wang Y, Ren H, Wang Q, Li S, Lu Y, Masu W, et al.
Let-7c-5p/IGF2BP1 axis in Oral Squamous Cell Carcinoma represses progressions in vitro. Trop J Pharm Res 2021; 20(12):2511-2518
doi:
10.4314/tjpr.v20i12.8
© 2021 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose: Oral squamous cell carcinoma (OSCC), a malignant tumor with high mortality, occurs in the head and neck. Let-7c-5p is involved in progression of many kinds of cancers. The purpose of this study was to determine the biological function of let-7c-5p in OSC.
Methods: RT-qPCR was performed to determine expressions of let-7c-5p and western blot measured protein expressions of IGF2BP1, E-cadherin, Vimentin and N-cadherin. Furthermore, dual-luciferase reporter test was used to evaluate the binding between IGF2BP1 and let-7c-5p. Moreover, MTT assay was employed to evaluate the cell viability while Transwell and Scratch assays were used to confirm cell metastasis. The cell apoptosis was validated using flow cytometry.
Results: Downregulation of let-7c-5p was recognized in OSCC cell lines. Let-7c-5p directly targeted and negatively modulated IGF2BP1. Other assays showed that let-7c-5p up-regulation had significant inhibitory roles on the cell viability, metastasis and tumor growth of OSSC cells. Additionally, EMT was also inhibited. Interestingly, upregulated let-7c-5p promoted apoptosis. Consequently, the abnormal expression of IGF2BP1 reversed functions of up-regulated let-7c-5p in OSCC cells.
Conclusion: These findings suggested that let-7c-5p behaves as an inhibitor regulating OSCC cell proliferation and migratory ability, which contributes to treatments by targeting IGF2BP1 in patients suffered from OSCC.
Keywords: Let-7c-5p, IGF2BP1, OSCC, Suppressor.