Targeting DNA repair as a promising approach in cancer therapy

被引:80
作者
Damia, Giovanna [1 ]
D'Incalci, Maurizio [1 ]
机构
[1] Ist Ric Farmacol Mario Negri, Dept Oncol, I-20157 Milan, Italy
关键词
DNA repair; anticancer drugs;
D O I
10.1016/j.ejca.2007.05.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
An increased DNA-repair activity in tumour cells has been associated with resistance to treatment to DNA-directed drugs, while defects in DNA repair pathways result in hypersensitivity to these agents. In the past years the unravelling of the molecular basis of these DNA pathways, with a better understanding of the DNA damage caused by different anticancer agents, has provided the rationale for the use of some DNA repair inhibitors to optimise the therapeutic use of DNA-damaging agents currently used in the treatment of tumours. In addition, the possibility to specifically target the differences in DNA repair capacity between normal and tumour cells has recently emerged as an exciting possibility. The present review will mainly cover those approaches that are currently under clinical investigation (C) 2007 Published by Elsevier Ltd
引用
收藏
页码:1791 / 1801
页数:11
相关论文
共 97 条
[61]   Targeting the double-strand DNA break repair pathway as a therapeutic strategy [J].
Lord, Christopher J. ;
Garrett, Michelle D. ;
Ashworth, Alan .
CLINICAL CANCER RESEARCH, 2006, 12 (15) :4463-4468
[62]  
LUO M, 2004, P AM ASSOC CANC RES, V45, P3042
[63]   New opportunities in chemosensitization and radiosensitization: modulating the DNA-damage response [J].
Luo, Y ;
Leverson, JD .
EXPERT REVIEW OF ANTICANCER THERAPY, 2005, 5 (02) :333-342
[64]   The emerging role of DNA repair proteins as predictive, prognostic and therapeutic targets in cancer [J].
Madhusudan, S ;
Middleton, MR .
CANCER TREATMENT REVIEWS, 2005, 31 (08) :603-617
[65]   DNA repair inhibition: a selective tumour targeting strategy [J].
Madhusudan, S ;
Hickson, ID .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (11) :503-511
[66]   Isolation of a small molecule inhibitor of DNA base excision repair [J].
Madhusudan, S ;
Smart, F ;
Shrimpton, P ;
Parsons, JL ;
Gardiner, L ;
Houlbrook, S ;
Talbot, DC ;
Hammonds, T ;
Freemont, PA ;
Sternberg, MJE ;
Dianov, GL ;
Hickson, ID .
NUCLEIC ACIDS RESEARCH, 2005, 33 (15) :4711-4724
[67]   Improvement of chemotherapy efficacy by inactivation of a DNA-repair pathway [J].
Middleton, MR ;
Margison, GP .
LANCET ONCOLOGY, 2003, 4 (01) :37-44
[68]   DNA repair by ERCC1 in non-small-cell lung cancer and cisplatin-based adjuvant chemotherapy [J].
Olaussen, Ken A. ;
Dunant, Ariane ;
Fouret, Pierre ;
Brambilla, Elisabeth ;
Andre, Fabrice ;
Haddad, Vincent ;
Taranchon, Estelle ;
Filipits, Martin ;
Pirker, Robert ;
Popper, Helmut H. ;
Stahel, Rolf ;
Sabatier, Laure ;
Pignon, Jean-Pierre ;
Tursz, Thomas ;
Le Chevalier, Thierry ;
Soria, Jean-Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (10) :983-991
[69]  
PEGG AE, 1990, CANCER RES, V50, P6119
[70]   Inhibition of poly(ADP-ribose) pollyrnerase in cancer [J].
Plummer, Elizabeth Ruth .
CURRENT OPINION IN PHARMACOLOGY, 2006, 6 (04) :364-368