Does ionizing radiation stimulate cancer invasion and metastasis?

被引:105
作者
Madani, Indira [1 ]
De Neve, Wilfried [1 ]
Mareel, Marc [1 ]
机构
[1] State Univ Ghent Hosp, Dept Radiotherapy, B-9000 Ghent, Belgium
关键词
radiotherapy; metastasis; tumor-associated host cells; pro-invasive signaling; tumor ecosystems;
D O I
10.1684/bdc.2008.0598
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiotherapy (RT) is a form of local treatment used mainly for malignant tumors. Such tumors originate from mutated stein cells, During their development they do attract a variety of host cells, coined tumor-associated host cells. Malignant tumors are characterized by uncontrolled growth,. invasion and metastasis'. the latter being the major cause of death of patients, even when their primary tumor is under control. RT inhibits growth. There are, however. clinical data suggesting that, under some circumstances, it may stimulate metastasis. DNA is a target of ionizing radiation (IR), though not the only one. IR produces cascades of growth factors and chemokines; it activates molecules initiating multiple signaling pathways that modulate several cellular Junctions. We consider cancer as a network of ecosystems, including at least the founder primary tumor, the site of metastasis and the hone marrow. As these ecosystems are in continuous communication, it is not surprising that R T of the primary tumor influences metastasis. Indeed, experiments with cells in culture and with animal tumors have shown that IR stimulates invasion and metastasis and activates pro-invasive and prometastatic cellular activities through upregulation of key molecules. At certain doses and within certain time frames, IR enhances the activities of the tumor-associated host cells that support invasion and metastasis, namely: endothelial cells building new vessels; leucocytes and macrophages causing inflammation; myofibroblasts initiating desmoplasia; osteoblasts and osteoclasts establishing hone metastasis; nerve cells producing efferent growth- and invasion-promoting molecules. Techniques such as spatially fractioned radiotherapy and hadron therapy may have different effects on metastasis. Taking into consideration the dose- and time-dependency of the IR-induced tumor-associated host cell reactions, these techniques, as well as the conventional ones, should he combined with repetitive biological imaging, reevaluation of planning and eventual replanning during the course of the treatment.
引用
收藏
页码:292 / 300
页数:9
相关论文
共 55 条
[1]   Inhibition of αvβ3 integrin survival signaling enhances antiangiogenic and antitumor effects of radiotherapy [J].
Abdollahi, A ;
Griggs, DW ;
Zieher, H ;
Roth, A ;
Lipson, KE ;
Saffrich, R ;
Gröne, HJ ;
Hallahan, DE ;
Reisfeld, RA ;
Debus, J ;
Niethammerl, AG ;
Huber, PE .
CLINICAL CANCER RESEARCH, 2005, 11 (17) :6270-6279
[2]   Radiation and the microenvironment - Tumorigenesis and therapy [J].
Barcellos-Hoff, MH ;
Park, C ;
Wright, EG .
NATURE REVIEWS CANCER, 2005, 5 (11) :867-875
[3]   Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck [J].
Bonner, JA ;
Harari, PM ;
Giralt, J ;
Azarnia, N ;
Shin, DM ;
Cohen, RB ;
Jones, CU ;
Sur, R ;
Raben, D ;
Jassem, J ;
Ove, R ;
Kies, MS ;
Baselga, J ;
Youssoufian, H ;
Amellal, N ;
Rowinsky, EK ;
Ang, KK .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :567-578
[4]   Hyperfractionated accelerated chemoradiation with concurrent fluorouracil-mitomycin is more effective than dose-escalated hyperfractionated accelerated radiation therapy alone in locally advanced head and neck cancer: Final results of the radiotherapy cooperative clinical trials group of the German cancer society 95-06 prospective randomized trial [J].
Budach, V ;
Stuschke, M ;
Budach, W ;
Baumann, M ;
Geismar, D ;
Grabenbauer, G ;
Lammert, I ;
Jahnke, K ;
Stueben, G ;
Herrmann, T ;
Bamberg, M ;
Wust, P ;
Hinkelbein, W ;
Wernecke, KD .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (06) :1125-1135
[5]  
Camphausen K, 2001, CANCER RES, V61, P2207
[6]   Noninvasive monitoring of radiotherapy-induced microvascular changes using dynamic contrast enhanced magnetic resonance imaging (DCE-MRI) in a colorectal tumor model [J].
Ceelen, W ;
Smeets, P ;
Backes, W ;
Van Damme, N ;
Boterberg, T ;
Demetter, P ;
Bouckenooghe, I ;
De Visschere, M ;
Peeters, M ;
Pattyn, P .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 64 (04) :1188-1196
[7]   Role of tissue stroma in cancer cell invasion [J].
De Wever, O ;
Mareel, M .
JOURNAL OF PATHOLOGY, 2003, 200 (04) :429-447
[8]  
ENGEBRAATEN O, 1992, ANTICANCER RES, V12, P1501
[9]   Bone marrow origin of myofibroblasts in irradiation pulmonary fibrosis [J].
Epperly, MW ;
Guo, HL ;
Gretton, JE ;
Greenberger, JS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 29 (02) :213-224
[10]   Engaging the vascular component of the tumor response [J].
Fuks, Z ;
Kolesnick, R .
CANCER CELL, 2005, 8 (02) :89-91