Modulation of rodent spinal cord radiation tolerance by administration of platelet-derived growth factor

被引:18
作者
Andratschke, NH
Nieder, C
Price, RE
Rivera, B
Tucker, SL
Ang, KK
机构
[1] Tech Univ Munich, Dept Radiat Oncol, Klinikum Rechts Isar, D-81675 Munich, Germany
[2] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Vet Med & Surg, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Biomath, Houston, TX 77030 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2004年 / 60卷 / 04期
关键词
spinal cord; radiation therapy; radiation myelopathy; radiation tolerance; platelet-derived growth factor;
D O I
10.1016/j.ijrobp.2004.07.703
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To examine the role of platelet-derived growth factor (PDGF) for ameliorating radiation myelopathy of the cervical spinal cord in a rodent model. Methods and Materials: After developing the technique for cannulation of the basal cistern, initial animal experiments were conducted to test the feasibility of intrathecal continuous infusion of PDGF in a model of cervical spinal cord irradiation in adult Fisher F-344 rats and to determine the most effective dose level of PDGF. Subsequently, the dose-modification factor was determined in a larger group of rats. Irradiation was given in 2 fractions (16 Gy followed by 14-24 Gy) and animals were examined for the development of paresis. Results: The initial dose-finding experiment revealed significant differences in the incidence of radiation myelopathy (100% in saline-treated control rats, 25% with the most effective dose of PDGF, up to 100% with less effective doses). The most effective dose of PDGF was 0.014 mug per day. Subsequent experiments revealed a median effective dose (ED50) of 35.6 Gy (95% confidence interval, 34.7-36.5 Gy) for animals receiving this dose of PDGF in contrast to 33.8 Gy (33.4-34.3 Gy) for the control group (p = 0.003). The dose-modification factor obtained with this dose of PDGF was 1.05. Conclusions: Intrathecal administration of PDGF concomitant to irradiation of the cervical spinal cord in rats was feasible. Treatment with PDGF significantly increased the tolerance of the spinal cord. The PDGF experiments should be viewed as a proof of principle that brief therapeutic intervention in the earliest phase of damage induction can reduce late effects in the spinal cord. They form the basis for further studies of growth factor administration in this particular model. (C) 2004 Elsevier Inc.
引用
收藏
页码:1257 / 1263
页数:7
相关论文
共 41 条
[1]   A single intracerebral microinjection of platelet-derived growth factor (PDGF) accelerates the rate of remyelination in vivo [J].
Allamargot, C ;
Pouplard-Barthelaix, A ;
Fressinaud, C .
BRAIN RESEARCH, 2001, 918 (1-2) :28-39
[2]  
Ang K K, 1984, Radiother Oncol, V1, P247
[3]   Extent and kinetics of recovery of occult spinal cord injury [J].
Ang, KK ;
Jiang, GL ;
Feng, Y ;
Stephens, LC ;
Tucker, SL ;
Price, RE .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 50 (04) :1013-1020
[4]   INHALATION ANESTHESIA IN EXPERIMENTAL RADIOTHERAPY - A RELIABLE AND TIME-SAVING SYSTEM FOR MULTIFRACTIONATION STUDIES IN A CLINICAL DEPARTMENT [J].
ANG, KK ;
VANDERKOGEL, AJ ;
VANDERSCHUEREN, E .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1982, 8 (01) :145-148
[5]   THE EFFECTS OF PLATELET-DERIVED GROWTH-FACTOR IN CULTURED MICROVESSEL ENDOTHELIAL-CELLS [J].
BAR, RS ;
BOES, M ;
BOOTH, BA ;
DAKE, BL ;
HENLEY, S ;
HART, MN .
ENDOCRINOLOGY, 1989, 124 (04) :1841-1848
[6]   Reirradiation of primary CNS tumors [J].
Bauman, GS ;
Sneed, PK ;
Wara, WM ;
Stalpers, LJA ;
Chang, SM ;
McDermott, MW ;
Gutin, PH ;
Larson, DA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1996, 36 (02) :433-441
[7]   PLATELET-DERIVED GROWTH-FACTOR EXPRESSION AND STIMULATION IN HUMAN MENINGIOMAS [J].
BLACK, PM ;
CARROLL, R ;
GLOWACKA, D ;
RILEY, K ;
DASHNER, K .
JOURNAL OF NEUROSURGERY, 1994, 81 (03) :388-393
[8]   Oligodendrocyte population dynamics and the role of PDGF in vivo [J].
Calver, AR ;
Hall, AC ;
Yu, WP ;
Walsh, FS ;
Heath, JK ;
Betsholtz, C ;
Richardson, WD .
NEURON, 1998, 20 (05) :869-882
[9]   Endothelial signaling during development [J].
Cleaver, O ;
Melton, DA .
NATURE MEDICINE, 2003, 9 (06) :661-668
[10]   Tumor growth and tumor radiosensitivity in mice given myeloprotective doses of fibroblast growth factors [J].
Ding, I ;
Huang, KD ;
Snyder, ML ;
Cook, J ;
Zhang, L ;
Wersto, N ;
Okunieff, P .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (19) :1399-1404