The effect of 5μm benzoquinone on cxcl12 and kitlg genes in mesenchymal stem cells found in bone marrow niche

Razieh Tavakoli,1,* Dr.majid sadeghizadeh,2

Abstract


Introduction

Chronic exposure to benzene is known to damage the bm resulting in development of different types of leukemia. extrinsic signaling cues in the microenvironment of acute myelogenous leukemia (aml) contribute to disease progression and therapy resistance . mesenchymal stem cells derived from adult bone marrow (bm-mscs), providing both cell sources for connective tissues and the control of hematopoiesis via secretion important elements of hematopoietic niche. niches are local tissue microenvironments that maintain and regulate stem cells. previous studies have showed that benzene is one of the important risk factors for aml. this study aimed to evaluate the low doses of benzene on the expression levels of some cancer related genes including cxcl12 and kitlg in mscs.

Methods

Mscs obtained from a healthy volunteer and cultured in the proper medium. after confirmation of mscs with standard methods, cells were exposed to 5 and 10 mm of benzene and the expression of kitlg and cxcl12 genes evaluated by real time pcr method.

Results

The results indicate that increased expression of kitlg and cxcl12 genes specifically under 5 mm concentration of benzene.

Conclusion

The scf (kitlg)-kit signaling pathways and the cxcl12-cxcl4 axis both are important factors for the bone marrow niche. according to this study and based on the specific role of these genes in cancer and the control of niche, benzene is one of the main factors of carcinogenesis even in the low doses. thus, hematopoietic niche and eventually leukemia are caused by changes in the expression of these genes.

Keywords

Benzene, benzoquinon, mesenchimal stem cells, kitlg, cxcl12