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Imatinib alters cell viability but not growth factors levels in TM4 Sertoli cells
Seyyed Mohammad Reza Hashemnia1, Somayeh Atari-Hajipirloo1, Shiva Roshan-Milani1
1Department of Biochemistry, Tehran University of Medical Sciences and Urmia University of Medical Sciences, Urmia and Tehran, Iran.
Background:
The anticancer agent imatinib (IM) is a small molecular analog of ATP that inhibits tyrosine kinase activity of platelet derived growth factors (PDGFs) and stem cell factor (SCF) receptor in cancer cells. However these factors have a key role in regulating growth and development of normal Sertoli, Leydig and germ cells.
Objective:
The aim of this study was to determine cell viability, PDGF and SCF levels in mouse normal Sertoli cells exposed to IM.
Materials And Methods:
In this experimental study, the mouse TM4 Sertoli cells were treated with 0, 2.5, 5, 10 and 20 μM IM for 2, 4 or 6 days. The cell viability and growth factors levels were assessed by MTT and ELISA methods, respectively. For statistical analysis, One-Way ANOVA was performed.
Results:
IM showed significant decrease in Sertoli cell viability compared to control group (p=0.001). However, IM increased PDGF and SCF level insignificantly (p>0.05).
Conclusion:
Results suggested that IM treatment induced a dose dependent reduction of cell viability in Sertoli cells. It seems that treatment with this anticancer drug is involved in the fertility process. Further studies are needed to evaluate the role of PDGF and SCF in this cell.
Insights
The anticancer drug imatinib (IM) significantly reduced Sertoli cell viability in mice. While IM increased platelet-derived growth factor (PDGF) and stem cell factor (SCF) levels, its impact on male fertility requires further investigation.
Area of Science:
- Reproductive Biology
- Cancer Therapeutics
- Cell Biology
Background:
- Imatinib (IM) is an ATP-competitive tyrosine kinase inhibitor used in cancer therapy.
- IM targets platelet-derived growth factors (PDGFs) and stem cell factor (SCF) receptors, crucial for cancer cell proliferation.
- PDGF and SCF also play vital roles in the development and function of normal testicular cells, including Sertoli cells.
Purpose of the Study:
- To investigate the effects of imatinib (IM) on the viability of normal mouse Sertoli cells.
- To assess the impact of IM on the levels of PDGF and SCF in Sertoli cells.
- To explore the potential implications of IM treatment on male reproductive health.
Main Methods:
- Mouse TM4 Sertoli cells were exposed to varying concentrations of IM (0-20 μM) for 2, 4, or 6 days.
- Cell viability was quantified using the MTT assay.
- Levels of PDGF and SCF were measured via ELISA.
- Statistical significance was determined using One-Way ANOVA.
Main Results:
- Imatinib (IM) treatment resulted in a statistically significant decrease in Sertoli cell viability in a dose-dependent manner (p=0.001).
- IM exposure led to an insignificant increase in PDGF and SCF levels compared to the control group (p>0.05).
Conclusions:
- Imatinib induces a dose-dependent reduction in Sertoli cell viability.
- The study suggests a potential link between imatinib treatment and male fertility.
- Further research is warranted to elucidate the specific roles of PDGF and SCF in IM-affected Sertoli cells and their contribution to fertility processes.
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