Startseite Lebenswissenschaften Assessment of AXL and mTOR genes expression in medullary thyroid carcinoma (MTC) cell line in relation with over expression of miR-144 and miR-34a
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Assessment of AXL and mTOR genes expression in medullary thyroid carcinoma (MTC) cell line in relation with over expression of miR-144 and miR-34a

  • Shaghayegh Pishkari , Razie Hadavi ORCID logo , Ameneh Koochaki ORCID logo , Javad Razaviyan ORCID logo , Mahdi Paryan ORCID logo , Mehrdad Hashemi ORCID logo und Samira Mohammadi-Yeganeh ORCID logo EMAIL logo
Veröffentlicht/Copyright: 26. März 2021

Abstract

Objectives

The aim of the present study was to investigate the expression of AXL and mTOR genes and their targeting microRNAs (miRNAs) including miR-34a and miR-144 in Medullary Thyroid Carcinoma (MTC) cell line, TT, and determine the effect of these two miRNAs on their target genes to introduce new molecular markers or therapeutics.

Methods

The expression of miR-34a, miR-144, and their targets genes including AXL and mTOR was evaluated by quantitative Real-time PCR. Luciferase assay was performed to confirm the interaction between miRNAs and their target mRNAs. The expression level of AXL and mTOR was evaluated before and after miRNAs induction in TT cell line compared with Cos7 as control cells.

Results

The expression of AXL and mTOR were up-regulated significantly, while miR-34a and miR-144 were down-regulated in TT cell line compared to Cos7. After transduction, the overexpression of miR-34a and 144 caused down-regulation of both genes. Luciferase assay results showed that the mTOR is targeted by miR-34a and miR-144 and the intensity of luciferase decreased in the presence of miRNAs.

Conclusions

Based on the results of the present study and since AXL and mTOR genes play a critical role in variety of human cancers, suppression of these genes by their targeting miRNAs, especially miR-34a and miR-144, can be propose as a new strategy for MTC management. However, more studies are needed to approve the hypothesis.


Corresponding author: Samira Mohammadi-Yeganeh, Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; and Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran, Phone: (+98)21 22439957, Fax: (+98)21 22439956, E-mail:

Acknowledgments

The authors thank the Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences and also Pasteur Institute of Iran, Tehran, Iran for providing technical support.

  1. Research funding: This project was funded by the Shahid Beheshti University of Medical Sciences, Tehran, Iran.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors declare no conflict of interest.

  4. Informed consent: Not applicable.

  5. Ethical approval: Not applicable.

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Received: 2020-07-21
Accepted: 2021-02-21
Published Online: 2021-03-26

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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