Akademik Veri Yönetim Sistemi
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, cilt.141, ss.26-36, 2014 (SCI-Expanded)
It has been reported that NKX3.1 an androgen-regulated homeobox gene restricted to prostate and testicular tissues, encodes a homeobox protein, which transcriptionally regulates oxidative damage responses and enhances topoisomerase I re-ligation by a direct interaction with the ATM protein in prostate cells. In this study, we aimed to investigate the role of NICX3.1 in DNA doublestrand break (DSB) repair. We demonstrate that the DNA damage induced by CPT-11 (irinotecan, a topo I inhibitor), doxorubicin (a topo II inhibitor), and H2O2 (a mediator of oxidative damage), but not by etoposide (another topo II inhibitor), is negatively influenced by NIOC3.1 expression. We also examined gamma H2Ak((s139)) foci formation and observed that the overexpression of NIOC3.1 resulted a remarkable decrease in the formation of gamma H2AX((s139)) foci. Intriguingly, we observed in NICX3.1 silencing studies that the depletion of NICX3.1 correlated with a significant decrease in the levels of p-ATM((s1981)) and gamma H2AX((5139)). The data imply that the DNA damage response (DDR) can be altered, perhaps via a decrease in the topoisomerase I re-ligation function; this is consistent with the physical association of NICX3.1 with DDR mediators upon treatment of both PC-3 and LNCaP cells with CPT-11. Furthermore, the depletion of NKX3.1 resulted in a G1/S progression via the facilitation of an increase in E2F stabilization concurrent with the suppressed DDR. Thus, the topoisomerase I inhibitor-mediated DNA damage enhanced the physical association of NIOC3.1 with gamma TH2AX((5139)) on the chromatin in LNCaP cells, whereas NKX3.1 in the soluble fraction was associated with p-ATM((s1981)) and RAD50 in these cells. Overall, the data suggest that androgens and NKX3.1 expression regulate the progression of the cell cycle and concurrently activate the DDR. Therefore, androgen withdrawal may augment the development of an error-prone phenotype and, subsequently, the loss of DNA damage control during prostate cancer progression. (C) 2014 Elsevier Ltd. All rights reserved.