Title of article :
Emerging Effects of Sepantronium Bromide (YM155) on MOLT-4 Cell Line Apoptosis Induction and Expression of Critical Genes Involved in Apoptotic Pathways
Author/Authors :
Shojaei Moghadam, Kobra Student Research Committee - Tabriz University of Medical Sciences, Tabriz - Immunology Research Center - Tabriz University of Medical Sciences , Farshdousti Hagh, Majid Drug Applied Research Center - Tabriz University of Medical Sciences , Alivand, Mohammad Reza Department of Medical Genetic - Tabriz University of Medical Sciences , Fardi, Masoumeh Student Research Committee - Tabriz University of Medical Sciences, Tabriz - Immunology Research Center - Tabriz University of Medical Sciences , Movassaghpour, Ali Akbar Hematology and Oncology Research Center - Tabriz University of medical Sciences , Mohammadi, Ali Departments of Cancer and Inflammation Research - Institute of Molecular Medicine - University of Southern Denmark - Odense, Denmark , Moghadasi, Maryam Student Research Committee - Tabriz University of Medical Sciences, Tabriz , Solali, Saeed Molecular Medicine Research Center - Tabriz University of Medical Science - Division of Hematology and Transfusion Medicine - Department of Immunology - Faculty of Medicine - Tabriz University of Medical Sciences
Abstract :
Purpose: Sepantronium bromide (YM155) is a Survivin inhibitor which recently advanced as an
anticancer agent in phase II clinical trials. Survivin belongs to IAP (inhibitor of apoptosis) gene
family and is a pivotal target for treatment due to its overexpression and oncogenic function
in many malignancies, including acute lymphoblastic leukemia (ALL). Although survivin is a
specific target for YM155, recent reports have shown that it has many other crucial targets that
regulate its anti-apoptotic effects. The aim of this study was to investigate whether YM155 could
have an effect on cell death-inducing genes as well as inducing apoptosis in T-ALL MOLT4- cell
line.
Methods: We treated MOLT-4 cells with increasing concentrations of YM155 and then cell
viability was determined using MTT (methyl thiazolyl tetrazolium) assay. Also, the rate of
induction of apoptosis in MOLT-4 cells and the target genes expression levels were evaluated by
Annexin V/PI and real-time PCR, respectively.
Results: YM155 inhibited cell growth in MOLT-4 cells. This outcome is achieved by inducing
apoptosis and a significant increase in the expression level of P53, MiR-9, caspase 3 and
decreasing the mRNA expression levels of survivin, Sirtuin1(SIRT1), member of anti-apoptotic
proteins family (Bcl-2), and epithelial-to-mesenchymal transition (EMT) initiating factors
Snail1and Zeb2.
Conclusion: The results showed that use of YM155 can be a potential drug therapy in T-ALL
patients with promising effects on apoptosis induction.
Keywords :
Apoptosis , Cancer , Drug , Survivin , MOLT-4 , YM155
Journal title :
Advanced Pharmaceutical Bulletin