Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/4938
Title: NKX3.1 contributes to S phase entry and regulates DNA damage response (DDR) in prostate cancer cell lines
Authors: Erbaykent Tepedelen, Burcu
Özmen, Besra
Varışlı, Lokman
Gönen Korkmaz, Ceren
Debeleç Bütüner, Bilge
Hamid, Syed Muhammad
Çakmak, Özgür Yılmazer
Korkmaz, Kemal Sami
Çakmak, Özgür Yılmazer
Izmir Institute of Technology. Biotechnology and Bioengineering Research and Application Center (IZTECH BIYOMER)
Keywords: NKX3.1
PATM (S1981)
Prostate cancer
Topoisomerase inhibitor CPT-11
DNA damage response
γH2AX (S139) foci
Issue Date: Oct-2011
Publisher: Academic Press Inc.
Source: Erbaykent-Tepedelen, B., Özmen, B., Varışlı, L., Gönen-Korkmaz, C., Debeleç-Bütüner, B., Hamid, S. M., Çakmak, Ö. Y., and Korkmaz, K. S. (2011). NKX3.1 contributes to S phase entry and regulates DNA damage response (DDR) in prostate cancer cell lines. Biochemical and Biophysical Research Communications, 414(1), 123-128. doi:10.1016/j.bbrc.2011.09.035
Abstract: NKX3.1 is an androgen-regulated homeobox gene that encodes a tissue-restricted transcription factor, which plays an important role in the differentiation of the prostate epithelium. Thus, the role of NKX3.1 as a functional topoisomerase I activity enhancer in cell cycle regulation and the DNA damage response (DDR) was explored in prostate cancer cell lines. As an early response to DNA damage following CPT-11 treatment, we found that there was an increase in the γH2AX (S139) foci number and that total phosphorylation levels were reduced in PC-3 cells following ectopic NKX3.1 expression as well as in LNCaP cells following androgen administration. Furthermore, upon drug treatment, the increase in ATM (S1981) phosphorylation was reduced in the presence of NKX3.1 expression, whereas DNA-PKcs expression was increased. Additionally, phosphorylation of CHK2 (T68) and NBS1 (S343) was abrogated by ectopic NKX3.1 expression, compared with the increasing levels in control PC-3 cells in a time-course experiment. Finally, NKX3.1 expression maintained a high cyclin D1 expression level regardless of drug treatment, while total γH2AX (S139) phosphorylation remained depleted in PC-3, as well as in LNCaP, cells. Thus, we suggest that androgen regulated NKX3.1 maintains an active DDR at the intra S progression and contributes to the chemotherapeutic resistance of prostate cancer cells to DNA damaging compounds.
URI: http://doi.org/10.1016/j.bbrc.2011.09.035
http://hdl.handle.net/11147/4938
ISSN: 0006-291X
0006-291X
Appears in Collections:IZTECH Research Centers Collection / İYTE Araştırma Merkezleri Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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