Evaluation of the anti-vascular effects of combretastatin in rodent tumours by dynamic contrast enhanced MRI

被引:90
作者
Maxwell, RJ
Wilson, J
Prise, VE
Vojnovic, B
Rustin, GJ
Lodge, MA
Tozer, GM
机构
[1] Mt Vernon Hosp, Gray Canc Inst, Northwood HA6 2JR, Middx, England
[2] Mt Vernon Hosp, Canc Treatment Ctr, Northwood HA6 2RN, Middx, England
[3] Mt Vernon Hosp, Paul Strickland Scanner Ctr, Northwood HA6 2RN, Middx, England
关键词
D O I
10.1002/nbm.754
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The anti-vascular effects of the tubulin binding agent, disodium combretastatin A-4 3-O-phosphate (CA-4-P). have been investigated in the rat P22 carcinosarcoma by measurements of radiolabelled iodoantipyrine uptake and dynamic contrast-enhanced MRI. The iodoantipyrine estimates of absolute tumour blood flow showed a reduction from 0.35 to 0.04 ml g(-1) min(-1) 6 h after 10 mg kg(-1) CA-4-P and to <0.01 ml g(-1) min(-1) after 100 mg kg(-1). Tumour blood flow, recovered to control values 24 h after 10 mg kg(-1) CA-4-P. but there was no recovery by 24 h after the higher dose. Dynamic contrast-enhanced MR images were obtained at 4.7 T, following injection of 0.1 mmol kg(-1) Gd-DTPA and analysed assuming a model arterial input function. A parameter, K(trans). which is related to blood flow rate and permeability of the tumour vasculature to Gd-DTPA, was calculated from the uptake data. K(trans) showed a reduction from 0.34 to 0.11 min(-1) 6 h after 10 mg kg(-1) CA-4-P and to 0.07 min(-1) after 100 mg kg(-1). Although the magnitude of changes in K(trans) was smaller than that in tumour blood flow, the time course and dose-dependency patterns were very similar. The apparent extravascular extracellular volume fraction, v(c), showed a four-fold reduction 6 h after 100 mg kg(-1) CA-4-P. possibly associated with vascular shutdown within large regions of the tumour. These results suggest that K(trans) Values for Gd-DTPA uptake into tumours Could be a useful non-invasive indicator of blood now changes induced by anti-vascular agents such as combretastatin, Copyright (C) 2002 John Wiley Sons, Ltd.
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页码:89 / 98
页数:10
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共 27 条
  • [1] Magnetic resonance imaging and spectroscopy of combretastatin A4 prodrug-induced disruption of tumour perfusion and energetic status
    Beauregard, DA
    Thelwall, PE
    Chaplin, DJ
    Hill, SA
    Adams, GE
    Brindle, KM
    [J]. BRITISH JOURNAL OF CANCER, 1998, 77 (11) : 1761 - 1767
  • [2] Chaplin DJ, 1999, BRIT J CANCER, V80, P57
  • [3] Quantification of the extraction fraction for gadopentetate across breast cancer capillaries
    Daldrup, HE
    Shames, DM
    Husseini, W
    Wendland, MF
    Okuhata, Y
    Brasch, RC
    [J]. MAGNETIC RESONANCE IN MEDICINE, 1998, 40 (04) : 537 - 543
  • [4] Dark GG, 1997, CANCER RES, V57, P1829
  • [5] Addressing tumor blood vessels
    Folkman, J
    [J]. NATURE BIOTECHNOLOGY, 1997, 15 (06) : 510 - 510
  • [6] Galbraith SM, 2000, BRIT J CANCER, V83, P12
  • [7] Gibaldi M. P., 1982, PHARMACOKINETICS
  • [8] In vivo and in vitro evaluation of combretastatin A-4 and its sodium phosphate prodrug
    Grosios, K
    Holwell, SE
    McGown, AT
    Pettit, GR
    Bibby, MC
    [J]. BRITISH JOURNAL OF CANCER, 1999, 81 (08) : 1318 - 1327
  • [9] KANTHOU C, 2001, P AACR ANN M
  • [10] Kety, 1960, METH MED RES, V8, P223