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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

Authors :
Razie Hadavi
Mehrdad Hashemi
Mahdi Paryan
Samira Mohammadi-Yeganeh
Javad Razaviyan
Ameneh Koochaki
Shaghayegh Pishkari
Source :
Hormone Molecular Biology and Clinical Investigation. 42:265-271
Publication Year :
2021
Publisher :
Walter de Gruyter GmbH, 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.

Details

ISSN :
18681891
Volume :
42
Database :
OpenAIRE
Journal :
Hormone Molecular Biology and Clinical Investigation
Accession number :
edsair.doi...........a1a3d61a2af3863c750232bd24b08730
Full Text :
https://doi.org/10.1515/hmbci-2020-0050