Apoptosis-inducing effect of spiroaminopyrimidine analogue in NB4 leukemia cells via down-regulation of BIRC5 expression

Authors

  • M.J. Dehghan Nayeri Department of Biology, Faculty of Natural Science, University of Tabriz, Tabriz 5166616471, Iran
  • M. Mahdavi Department of Biology, Faculty of Natural Science, University of Tabriz, Tabriz 5166616471, Iran
  • H. Fazeli Department of Microbiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan 817467346, Iran
  • M.A. Hosseinpour Feizi Department of Biology, Faculty of Natural Science, University of Tabriz, Tabriz 5166616471, Iran

DOI:

https://doi.org/10.32471/exp-oncology.2312-8852.vol-41-no-4.13749

Keywords:

apoptosis, cell cycle, NB4 cell line, spiroaminopyrimidine

Abstract

Summary. Aim: It has been reported that spiroaminopyrimidine derivatives inhibited the growth and proliferation of various cancer cell lines. In the present study, we evaluated cytotoxic and apoptosis-inducing effects of 2,4-diamino-1,3-diazaspiro[5.5]-9-tert-butyl-2, 4-diene-5-carbonitril (9-tBAP) on NB4 acute promyelocytic leukemia (APL) cells. Materials and Methods: The cells were treated with 10–100 µM of 9-tBAP. Cytotoxic activity of the compound was measured using the MTT assay. Apoptosis was investigated by Hoechst 33258 staining as well as by Annexin V/PI double staining. Results: The compound under study was found to be highly active cell growth inhibitor with IC50 of 30.0 ± 3.5 µM inducing apoptosis in NB4 cells. Cell cycle analysis by flow cytometry showed a time-dependent increase in sub-G1 cell population. Real-time polymerase chain reaction analysis revealed that the treatment with the compound down-regulated the BIRC5 expression in a time-dependent manner. Conclusion: 9-tBAP displayed potent anti-leukemic activity in vitro thus warranting further investigation.

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Published

02.06.2023

How to Cite

Dehghan Nayeri, M., Mahdavi, M., Fazeli, H., & Hosseinpour Feizi, M. (2023). Apoptosis-inducing effect of spiroaminopyrimidine analogue in NB4 leukemia cells via down-regulation of BIRC5 expression. Experimental Oncology, 41(4), 312–317. https://doi.org/10.32471/exp-oncology.2312-8852.vol-41-no-4.13749

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