Oxidative DNA Damage-Mediated Genomic Heterogeneity Is Regulated by NKX3.1 in Prostate Cancer

Abstract

The 8-hydroxy-2′-deoxyguanosine (8-OHdG) damages are base damages induced by reactive oxygen species. We aimed to investigate the role of Androgen Receptor and NKX3.1 in 8-OHdG formation and repair activation by quantitating the DNA damage using Aklides.NUK system.

The data demonstrated that the loss of NKX3.1 resulted in increased oxidative DNA damage and its overexpression contributes to the removal of menadione-induced 8-OHdG damage even under oxidative stress conditions. Moreover, 8-oxoguanine DNA glycosylase-1 (OGG1) expression level positively correlates to NKX3.1 expression. Also in this study, first time a reliable cell-based quantitation method for 8-OHdG damages is reported and used for data collection.

Keywords:

• 8-OHdG
• NKX3.1
• Androgen receptor
• Aklides

Disclosure statement

Dirk Roggenbuck is one of the shareholders of Generic Assays.GmbH and Medipan.GmbH being diagnostic manufacturers. The remaining authors declare no conflict of interest.

Additional information

Funding

This research is supported by a grant [113S044] from Turkish Scientific and Technology Research Council (TUBITAK) to KSK, and COST program EU-ROS, [BM1203] for mobility and data sharing.