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

DEBELEÇ BÜTÜNER B., Bostanci A., Ozcan F., Singin O., Karamil S., AYDIN ASLAN M., ...Daha Fazla

CANCER INVESTIGATION, cilt.37, sa.2, ss.113-126, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 37 Sayı: 2
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1080/07357907.2019.1576192
  • Dergi Adı: CANCER INVESTIGATION
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.113-126
  • Anahtar Kelimeler: 8-OHdG, NKX3, 1, Androgen receptor, Aklides, PHYSICAL-EXERCISE, ANDROGEN RECEPTOR, TOPOISOMERASE-I, REPAIR, GENE, 8-HYDROXY-2'-DEOXYGUANOSINE, ASSOCIATIONS, SENSITIVITY, BIOMARKER, STRESS
  • Akdeniz Üniversitesi Adresli: Evet

Özet

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.