Boric Acid Reduces the Formation of DNA Double Strand Breaks and Accelerates Wound Healing Process
No Thumbnail Available
Date
2016
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
Boron is absorbed by the digestive and respiratory system, and it was considered that it is converted to boric acid (BA), which was distributed to all tissues above 90 %. The biochemical essentiality of boron element is caused by boric acid because it affects the activity of several enzymes involved in the metabolism. DNA damage repair mechanisms and oxidative stress regulation is quite important in the transition stage from normal to cancerous cells; thus, this study was conducted to investigate the protective effect of boric acid on DNA damage and wound healing in human epithelial cell line. For this purpose, the amount of DNA damage occurred with irinotecan (CPT-11), etoposide (ETP), doxorubicin (Doxo), and H2O2 was determined by immunofluorescence through phosphorylation of H2AX(Ser139) and pATM(Ser1981) in the absence and presence of BA. Moreover, the effect of BA on wound healing has been investigated in epithelial cells treated with these agents. Our results demonstrated that H2AX(Ser139) foci numbers were significantly decreased in the presence of BA while wound healing was accelerated by BA compared to that in the control and only drug-treated cells. Eventually, the results indicate that BA reduced the formation of DNA double strand breaks caused by agents as well as improving the wound healing process. Therefore, we suggest that boric acid has important therapeutical effectiveness and may be used in the treatment of inflammatory diseases where oxidative stress and wound healing process plays an important role. © 2016, Springer Science+Business Media New York.
Description
Keywords
Ataxia Telangiectasia Mutated Proteins , Boric Acids , Cell Line , DNA Breaks, Double-Stranded , Epithelial Cells , Histones , Humans , Phosphorylation , Wound Healing , boric acid , cell protein , doxorubicin , etoposide , histone gammaH2AX , histone H2AX , hydrogen peroxide , irinotecan , pATM protein , unclassified drug , ATM protein , ATM protein, human , boric acid , histone , Article , cell migration , controlled study , DNA damage , double stranded DNA break , epithelium cell , histone phosphorylation , human , human cell , immunofluorescence , microscopy , MTT assay , oxidative stress , wound healing , cell line , double stranded DNA break , drug effects , metabolism , phosphorylation , wound healing