Author/Authors :
Moghimi, Mansour Department of Pathology - Shahid Sadoughi University of Medical Sciences, Yazd, Iran , Sadeghi Tafti, Hossein Department of Medical Laboratory Sciences - Shahid Sadoughi University of Medical Sciences, Yazd, Iran , Namazi, Faezeh Medical Biotechnology Research Center - Islamic Azad University, Ashkezar, Yazd, Iran , Salehi, Mansoor Medical Genetics Research Center of Genome, Mohtasham St., Isfahan, Iran
Abstract :
Background: Gliomas are a common type of the primary brain tumors and account for
more than 40% of all central nervous system (CNS) tumors. Glioblastoma (GBM) remains
one of the most fatal human malignancies as it is highly angiogenic. Foretinib is an
oral multikinase inhibitor that has been shown to exhibit antitumor activity in previous
clinical studies. AURKA and AURKB have been shown to be overexpressed in various
cancers.
The purpose of this study was to investigate the effect of foretinib on the expression
of AURKA and AURKB in the T98 cell line.
Materials and Methods: In this study, the T98 cell line was selected as an experimental
model of glioblastoma. The cultured cells were exposed to different concentrations
of foretinib (5 μM, 10 μM, 20 μM, and 0 μM as control). Following that, we examined
the changes in the expression of AURKA and AURKB under the influence of foretinib
compared to control using quantitative real-time polymerase chain reaction (qRT-PCR).
Results: The expression of AURKA and AURKB were found to be significantly reduced
in the foretinib treated group compared to the control. The results demonstrated that
increasing the concentration of foretinib led to reduction in the expression of both the
genes.
Conclusion: These findings indicate that the foretinib can decrease the mRNA levels
of AURKA and AURKB. Thus, we suggest that foretinib may be an effective drug for
GBM treatment and can be considered for future studies.
Keywords :
AURKA , AURKB , Foretinib , Glioblastoma