Induction of Cell Cycle Arrest in MKN45 Cells after Schiff Base Oxovanadium Complex Treatment Using Changes in Gene Expression of CdC25 and P53

Sara Mirjalili; Maedeh Dejamfekr; Abdolvahab Moshtaghian; Mehdi Salehi; Mahdi Behzad; Ali Khaleghian

doi:10.1055/a-1235-5565

Drug Research, Table of Contents

Drug Res (Stuttg) 2020; 70(12): 545-551
DOI: 10.1055/a-1235-5565

Original Article

Induction of Cell Cycle Arrest in MKN45 Cells after Schiff Base Oxovanadium Complex Treatment Using Changes in Gene Expression of CdC25 and P53

Authors

Sara Mirjalili

¹Department of Biochemistry, Semnan University of Medical Sciences, Semnan, Iran
Maedeh Dejamfekr

¹Department of Biochemistry, Semnan University of Medical Sciences, Semnan, Iran
Abdolvahab Moshtaghian

²Deputy of Research and Technology, Semnan University of Medical Sciences, Semnan, Iran
Mehdi Salehi

³Department of Chemistry, College of Science, Semnan University, Semnan, Iran
Mahdi Behzad

³Department of Chemistry, College of Science, Semnan University, Semnan, Iran
Ali Khaleghian

¹Department of Biochemistry, Semnan University of Medical Sciences, Semnan, Iran

Abstract

Compounds containing heavy metals such as vanadium, nickel, and cobalt may be useful for the treatment of various diseases. Multiple studies have been carried out on the anticancer effects of vanadium-contained compounds on different cell types. This study aimed to evaluate the role of schiff base oxovanadium complex ([N,N'-bis(3-methoxy-salicylidene)-1,2-phenylenediamine]Vanadium(IV) Oxide Complex) on cell cycle arrest and different cell cycle phases in MKN45 cell of gastric cancer. Schiff base oxovanadium complex was used to assessthe amount of cytotoxicity via cell viability test. PI color and flow cytometry technique were applied to evaluate the effects of vanadium synthetic compounds on cell cycle phases; subsequently, we analyzed the change rates of gene expression in P53, GADD45, and CDC25 genes, which are involved in cell division phases. The findings indicated that the vital activities of time-dependent and concentration-dependent MKN45 cells with schiff base oxovanadium complex were significantly reduced; therefore, this complex is able to inhibit the migration of cancer cells and metastatic activities in a time-dependent mode. Cell cycle arrest was obtained after 48 h of treatment in phase G2/M at 1 microgram/milliliter (μg/ml) concentration. This is probably attributed to the increased gene expression of P53 and GADD45 genes and reduced gene expression of CDC25 gene. Compounds containing such heavy metals as vanadium decrease the growth, proliferation, and migration of MKN45 cells. They arrest cell cycle in phase G2/M via changing the controllers of cell division phases activated due to DNA damage.

Key words

cell proliferation and malignancy - cancer - anticancer drugs

Full Text

References

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