Vascular perfusion and hypoxic areas in RIF-1 tumours after photodynamic therapy

• Published in: British journal of cancer Vol. 73; no. 3; pp. 288 - 293
• Main Authors: VAN GEEL, I. P. J, OPPELAAR, H, RIJKEN, P. F. J. W, BERNSEN, H. J. J. A, HAGEMEIER, N. E. M, VAN DER KOGEL, A. J, HODGKISS, R. J, STEWART, F. A
• Format: Journal Article
• Language: English
• Published: Basingstoke Nature Publishing Group 01.02.1996
• Subjects: Animals; Biological and medical sciences; Female; Hypoxia; Image Processing, Computer-Assisted; Medical sciences; Mice; Mice, Inbred C3H; Neoplasms, Experimental - blood supply; Photochemotherapy; Photoradiation therapy and photosensitizing agent; Treatment with physical agents; Treatment. General aspects; Tumors; Regional blood flow; Oxygen; Sarcoma; Rodentia; Malignant tumor; Phototherapy; Dye laser; In vivo; Vertebrata; Mammalia; Treatment; Mouse; Animal; Established cell line; Hypoxia; Photosensitizer; Quantitative analysis
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1996.51

The influence of photodynamic therapy (PDT) on vascular perfusion and the development of hypoxia was investigated in the murine RIF-1 tumour. Image analysis was used to quantify changes in perfusion and hypoxia at 5 min after interstitial Photofrin-mediated PDT. The fluorescent stain Hoechst 33342 was used as an in vivo marker of functional vascular perfusion and the antibody anti-collagen type IV as a marker of the tumour vasculature. The percentage of total tumour vasculature that was perfused decreased to less than 30% of control values after PDT. For the lower light doses this decrease was more pronounced in the centre of the tumour. The observed reduction in vascular perfusion showed a good linear correlation (r = 0.98) with previously published tumour perfusion data obtained with the 86Rb extraction technique. The image analysis technique provides extra information concerning the localisation of (non)-perfused vessels. To detect hypoxic tumour areas in vivo, an immunohistochemical method was used employing NITP [7-(4'-(2-nitroimidazol-1-yl)-butyl)-theophylline]. A large increase in hypoxic areas was found for PDT-treated tumours. More than half the total tumour area was hypoxic after PDT, compared with < 4% for control tumours. Our studies illustrate the potential of image analysis systems for monitoring the functional consequences of PDT-mediated vascular damage early after treatment. This provides direct confirmation that the perfusion changes lead to tissue hypoxia, which has implications for the combined treatment of PDT with bioreductive drugs.