Differential sensitivity of two adenocarcinoma xenografts to the anti-vascular drugs combretastatin A4 phosphate and 5,6-dimethylxanthenone-4-acetic acid, assessed using MRI and MRS

被引:53
作者
Beauregard, DA
Pedley, RB
Hill, SA
Brindle, KM
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[2] UCL, Royal Free & Univ Coll Med Sch, Dept Oncol, London NW3 2PF, England
[3] Mt Vernon Hosp, Gray Lab, Canc Res Trust, Northwood HA6 2JR, Middx, England
关键词
tumour; perfusion; combretastatin; DMXAA; magnetic resonance imaging;
D O I
10.1002/nbm.723
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The effects of two anti-vascular agents. combretastatin A4 phosphate (CA4P). and 5.6-dimethylxanthenone-4-acetic acid (DMXAA), on the perfusion Of two human colon adenocarcinomas implanted in SCID mice. were assessed for up to 3 h using non-invasive magnetic resonance imaging (MRI) and spectroscopy techniques (MRS), MRI measurements of GdDTPA inflow showed that treatment with CA4P had little effect on the perfusion of HT29 tumours. Localized (PMRS)-P-31 measurements also showed that the drug had no significant effect on tumour cell energy status, as assessed from the ratio of the integrals of the signals from inorganic phosphate (P-i) and nucleoside triphosphates. However. after treatment with DMXAA. perfusion was reduced and the P-i/NTP ratio increased. indicating that the HT29 tumour is susceptible to the action of this drug. The LS174T tumour model was susceptible to both CA4P and DMXAA. using the criteria of changes in GdDTPA inflow and P-i/NTP ratio. Copyright (C) 2002 John Wiley Sons. Ltd.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 27 条
[11]  
Galbraith SM, 2000, BRIT J CANCER, V83, P12
[12]  
GALBRAITH SM, 1998, BRIT J CANCER, V78, pO30
[13]  
Iyer S, 1998, CANCER RES, V58, P4510
[14]  
Joseph WR, 1999, CANCER RES, V59, P633
[15]   Quantitative diffusion imaging in implanted human breast tumors [J].
Maier, CF ;
Paran, Y ;
Bendel, P ;
Rutt, BK ;
Degani, H .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (04) :576-581
[16]   Combined effects of angiostatin and ionizing radiation in antitumour therapy [J].
Mauceri, HJ ;
Hanna, NN ;
Beckett, MA ;
Gorski, DH ;
Staba, MJ ;
Stellato, KA ;
Bigelow, K ;
Heimann, R ;
Gately, S ;
Dhanabal, M ;
Soff, GA ;
Sukhatme, VP ;
Kufe, DW ;
Weichselbaum, RR .
NATURE, 1998, 394 (6690) :287-291
[17]   Effects of combretastatin on murine tumours monitored by 31P MRS, 1H MRS and 1H MRI [J].
Maxwell, RJ ;
Nielsen, FU ;
Breidahl, T ;
Stodkilde-Jorgensen, H ;
Horsman, MR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 42 (04) :891-894
[18]  
Murata R, 2001, INT J RADIAT BIOL, V77, P195
[19]  
Pedley RB, 1996, CANCER RES, V56, P3293
[20]  
Pedley RB, 1999, CANCER RES, V59, P3998