Enhanced radiation response through directed molecular targeting approaches

被引:9
作者
Collis, SJ
DeWeese, TL [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Dept Radiat Oncol & Mol Radiat Sci, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Dept Urol, Baltimore, MD 21231 USA
关键词
ionizing radiation; gene therapy; radiosensitivity; molecular targeting; DNA damage and repair;
D O I
10.1023/B:CANC.0000031767.30730.d1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In both the pre- and post-human genome sequencing eras, there has been an increase in the understanding of the molecular mechanisms influencing cellular sensitivity to DNA damaging agents such as ionizing radiation. Out of this work have arisen many cellular factors that could be specifically targeted, at the molecular level, to alter the functionality of a single protein or pathway involved in the response to radiation damage as a means to increase cell killing following radiation treatment. As such, there are many promising new combination radio-gene therapy approaches being developed and assessed in pre- clinical and clinical studies for several different malignancies. Combination of such modalities aims to increase the therapeutic index, giving rise to increased tumor cell killing with a simultaneous reduction in normal cell toxicity. Restricted delivery and/or targeting modalities combined with conformal radiotherapy regimes could provide significant local control of tumors, impeding their development into metastatic disease, which poses a greater challenge for palliative and curative treatments. This review will summarize current and novel gene therapy strategies that are being developed aimed at enhancing the effects of radiotherapy through the use of directed molecular targeting approaches.
引用
收藏
页码:277 / 292
页数:16
相关论文
共 145 条
[71]   Combined-modality treatment of solid tumors using radiotherapy and molecular targeted agents [J].
Ma, BBY ;
Bristow, RG ;
Kim, J ;
Siu, LL .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) :2760-2776
[72]  
Maacke H, 2000, INT J CANCER, V88, P907, DOI 10.1002/1097-0215(20001215)88:6<907::AID-IJC11>3.0.CO
[73]  
2-4
[74]   DNA repair and recombination factor Rad51 is over-expressed in human pancreatic adenocarcinoma [J].
Maacke, H ;
Jost, K ;
Opitz, S ;
Miska, S ;
Yuan, Y ;
Hasselbach, L ;
Lüttges, J ;
Kalthoff, H ;
Stürzbecher, HW .
ONCOGENE, 2000, 19 (23) :2791-2795
[75]   Transfer of Ku86 RNA antisense decreases the radioresistance of human fibroblasts [J].
Marangoni, E ;
Le Romancer, M ;
Foray, N ;
Muller, C ;
Douc-Rasy, S ;
Vaganay, S ;
Abdulkarim, B ;
Barrois, M ;
Calsou, P ;
Bernier, J ;
Salles, B ;
Bourhis, J .
CANCER GENE THERAPY, 2000, 7 (02) :339-346
[76]   Gene expression - RNA interference in adult mice [J].
McCaffrey, AP ;
Meuse, L ;
Pham, TTT ;
Conklin, DS ;
Hannon, GJ ;
Kay, MA .
NATURE, 2002, 418 (6893) :38-39
[77]   Targeting tumor cells by enhancing radiation sensitivity [J].
McKenna, WG ;
Muschel, RJ .
GENES CHROMOSOMES & CANCER, 2003, 38 (04) :330-338
[78]  
Moreira JN, 2003, CURR OPIN MOL THER, V5, P547
[79]   Fragments of ATM which have dominant-negative or complementing activity [J].
Morgan, SE ;
Lovly, C ;
Pandita, TK ;
Shiloh, Y ;
Kastan, MB .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :2020-2029
[80]   DNA damage processing defects and disease [J].
Moses, RE .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2001, 2 :41-68