Alterations in the expression of the DNA repair/redox enzyme APE/ref-1 in epithelial ovarian cancers

被引:0
|
作者
Moore, D [1 ]
Michael, H [1 ]
Tritt, R [1 ]
Kelley, M [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Obstet & Gynecol, Indianapolis, IN 46204 USA
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The DNA base excision repair (BER) pathway is responsible for the repair of cellular alkylation and oxidative DNA damage. A crucial step in the BER pathway involves the cleavage of an apurinic/apyrimidinic site in DNA by an AP endonuclease. The major AP endonuclease in mammalian cells is APE/ref-1. We studied the expression of APE/ref-1 in formalin-fixed, paraffin-embedded ovarian tissue specimens using polyclonal and monoclonal antibodies to APE/ref-1. Compared to normal ovarian tissues, benign neoplastic conditions, and low malignant potential tumors, APE/ref-1 immunoreactivity is altered in malignant ovarian tumors. Further studies will determine if the altered expression reflects changes in DNA repair capabilities or redox regulatory functions.
引用
收藏
页码:263 / 267
页数:5
相关论文
共 50 条
  • [1] Alterations in the expression of the DNA repair/redox enzyme APE/ref-1 in epithelial ovarian cancers
    Moore, DH
    Michael, H
    Tritt, R
    Parsons, SH
    Kelley, MR
    CLINICAL CANCER RESEARCH, 2000, 6 (02) : 602 - 609
  • [2] Elevated and altered expression of the multifunctional DNA base excision repair and redox enzyme Ape1/ref-1 in prostate cancer
    Kelley, MR
    Cheng, L
    Foster, R
    Tritt, R
    Jiang, JZ
    Broshears, J
    Koch, M
    CLINICAL CANCER RESEARCH, 2001, 7 (04) : 824 - 830
  • [3] The Many Functions of APE1/Ref-1: Not Only a DNA Repair Enzyme
    Tell, Gianluca
    Quadrifoglio, Franco
    Tiribelli, Claudio
    Kelley, Mark R.
    ANTIOXIDANTS & REDOX SIGNALING, 2009, 11 (03) : 601 - 619
  • [4] The DNA repair activity of human redox/repair protein APE/Ref-1 is inactivated by phosphorylation
    Yacoub, A
    Kelley, MR
    Deutsch, WA
    CANCER RESEARCH, 1997, 57 (24) : 5457 - 5459
  • [5] The multifunctional DNA repair/redox enzyme Ape1/Ref-1 promotes survival of neurons after oxidative stress
    Vasko, MR
    Guo, C
    Kelley, MR
    DNA REPAIR, 2005, 4 (03) : 367 - 379
  • [6] Redox regulation of the DNA repair function of the human AP endonuclease Ape1/ref-1
    Kelley, MR
    Parsons, SH
    ANTIOXIDANTS & REDOX SIGNALING, 2001, 3 (04) : 671 - 683
  • [7] Alterations in the expression of the apurinic/apyrimidinic endonuclease-1/redox factor-1 (APE1/Ref-1) in human ovarian cancer and indentification of the therapeutic potential of APE1/Ref-1 inhibitor
    Zhang, Ying
    Wang, Jian
    Xiang, Debing
    Wang, Dong
    Xin, Xiaoyan
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 35 (05) : 1069 - 1079
  • [8] Knockdown of the DNA repair and redox signaling protein Ape1/Ref-1 blocks ovarian cancer cell and tumor growth
    Fishel, Melissa L.
    He, Ying
    Reed, April M.
    Chin-Sinex, Helen
    Hutchins, Gary D.
    Mendonca, Marc S.
    Kelley, Mark R.
    DNA REPAIR, 2008, 7 (02) : 177 - 186
  • [9] Enhancing the expression of the DNA repair/redox enzyme, Ape1/Ref-1, reduces neurotoxicity induced by ionizing radiation: Implications for decreasing neurocognitive dysfunction
    Vasko, Michael R.
    Guo, Chunlu
    Jiang, Yanlin L.
    Kelley, Mark R.
    PEDIATRIC BLOOD & CANCER, 2007, 48 (06) : 624 - 624
  • [10] Alterations in the expression of the apurinic/apyrimidinic endonuclease-1/redox factor-1 (APE/Ref-1) in human melanoma and identification of the therapeutic potential of resveratrol as an APE/Ref-1 inhibitor
    Yang, S
    Irani, K
    Heffron, SE
    Jurnak, F
    Meyskens, FL
    MOLECULAR CANCER THERAPEUTICS, 2005, 4 (12) : 1923 - 1935