Author/Authors :
Alizadeh، SH نويسنده Dept. of Surgery, Valiasr Hospital, Arak University of Medical Sciences, Arak, Iran , , Kaviani، A نويسنده Department of Hematology, Allied Medical School, Tehran University of Medical sciences, Tehran, Iran. , , Soleimani، M نويسنده Department of Hematology, Tarbiat Modares University, Tehran, Iran. , , Abroun، S نويسنده Department of Hematology, Tarbiat Modares University, Tehran, Iran. , , Kashani-Khatib، Z نويسنده Department of Hematology, Tarbiat Modares University, Tehran, Iran. , , Asgharzadeh، A نويسنده Department of Hematology, Mashad University of Medical sciences, Mashhad, Iran. , , Dargahi، H نويسنده Department of Health care services, Medical School, Tehran University of Medical sciences, Tehran, Iran. , , Mousavi، R نويسنده Department of Hematology, Allied Medical School, Tehran University of Medical sciences, Tehran, Iran. ,
Abstract :
Background
MicroRNAs are small and non-coding RNA
molecules with approximately 22 nt in length
that cause inhibition of translation or
degradation of mRNA. MiR-155 is a kind of
molecule with different functions, such as its
role in proliferation, apoptosis, inflammation,
differentiation, and immunity. One of its best
known functions is apoptosis that affects on
caspase-3 activity. The main aim of this study
was evaluation of miR-155 inhibition effect on
cell proliferation and apoptosis induction in
Jurkat cells.
Material and Methods
In this study, Jurkat cells along with MTT assay
were used for evaluation of sensitivity to varied
concentrations of miR-155 inhibitor (25, 50 and
75 nmol). MiR-155 expression level was
analyzed using the quantitative real-time
polymerase chain reaction (QRT-PCR).
Caspase-3 activity was measured by caspase-3
colorimetric activity assay kit. Unpaired ttest
was applied for the analysis of MTT and
apoptosis results. Probability of 5% was
assumed as statistically significant.
Results
According to our results, the use of miR-155
inhibitor increased the activity of caspase-3 by 2
fold in 75 nmol concentration. In this research,
we found that the proper increase of miR-155
inhibitor concentration can inhibit miR-155 and
consequently increase caspase-3 activity and
induce apoptosis in the Jurkat cells leading to
cell death ultimately.
Conclusions
Apoptosis induction by miRNAs activation or
inhibition is probably one of the best and low
risk ways of cell death induction in
malignancies. Due to role of miR-155 in several
cancer cells, it may be used as a therapeutic
target in future.
Key words: miRNA