Multiparameter analysis of vasculature, perfusion and proliferation in human tumour xenografts

被引:61
作者
Bussink, J
Kaanders, JHAM
Rijken, PFJW
Martindale, CA
van der Kogel, AJ
机构
[1] Univ Nijmegen, Inst Radiotherapy, NL-6500 HB Nijmegen, Netherlands
[2] Mt Vernon Hosp, Gray Lab Canc Res Trust, Northwood HA6 2JR, Middx, England
关键词
squamous cell carcinoma; glioblastoma; image analysis; proliferation; vasculature; perfusion;
D O I
10.1038/bjc.1998.9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A method is presented in this report for concurrent analysis of vascular architecture, blood perfusion and proliferation characteristics in whole-tumour cross-sections of human larynx carcinoma and glioblastoma xenografts. Tumours were implanted subcutaneously in nude mice. After i.v. injection with Hoechst 33342 and bromodeoxyuridine (BrdUrd) as perfusion and proliferation markers, animals were killed. An antiendothelial antibody (9F1) was used to delineate vascular structures. Cross-sections were analysed by a multistep immune staining and a computer-controlled microscope scanning method. Each tumour section was stained and scanned four times (Hoechst, 9F1, BrdUrd and Fast Blue for all nuclei). When these images were combined, vasculature, perfusion and proliferation parameters were analysed. The labelling index (LI) was defined as the ratio of the BrdUrd-labelled area to the total nuclear area. The LI based on manual counting and the LI calculated by flow cytometry (FCM) were in good agreement with the LI based on surface analysis. LI decreased at increasing distance from its nearest vessel. In the vicinity of perfused vessels, the LI was 30-70% higher than near non-perfused vessels. This method shows that both vasculature/perfusion and proliferation characteristics can be measured in the same whole-tumour section in a semiautomatic way. This could be applied in clinical practice to identify combined human tumour characteristics that predict for a favourable response to treatment modifications.
引用
收藏
页码:57 / 64
页数:8
相关论文
共 39 条
[1]  
ANG KK, 1996, RADIOTHER ONCOL S1, V40, pS30
[2]   CELL-KINETICS OF RAT 9L BRAIN-TUMORS DETERMINED BY DOUBLE LABELING WITH IODODEOXYURIDINE AND BROMODEOXYURIDINE [J].
ASAI, A ;
SHIBUI, S ;
BARKER, M ;
VANDERLAAN, M ;
GRAY, JW ;
HOSHINO, T .
JOURNAL OF NEUROSURGERY, 1990, 73 (02) :254-258
[3]   THE PREDICTIVE VALUE OF CELL KINETIC MEASUREMENTS IN A EUROPEAN TRIAL OF ACCELERATED FRACTIONATION IN ADVANCED HEAD AND NECK TUMORS - AN INTERIM-REPORT [J].
BEGG, AC ;
HOFLAND, I ;
MOONEN, L ;
BARTELINK, H ;
SCHRAUB, S ;
BONTEMPS, P ;
LEFUR, R ;
VANDENBOGAERT, W ;
CASPERS, R ;
VANGLABBEKE, M ;
HORIOT, JC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1990, 19 (06) :1449-1453
[4]   A METHOD TO MEASURE THE DURATION OF DNA-SYNTHESIS AND THE POTENTIAL DOUBLING TIME FROM A SINGLE SAMPLE [J].
BEGG, AC ;
MCNALLY, NJ ;
SHRIEVE, DC ;
KARCHER, H .
CYTOMETRY, 1985, 6 (06) :620-626
[5]   TUMOR PROLIFERATION ASSESSED BY COMBINED HISTOLOGICAL AND FLOW CYTOMETRIC ANALYSIS - IMPLICATIONS FOR THERAPY IN SQUAMOUS-CELL CARCINOMA IN THE HEAD AND NECK [J].
BENNETT, MH ;
WILSON, GD ;
DISCHE, S ;
SAUNDERS, MI ;
MARTINDALE, CA ;
ROBINSON, BM ;
OHALLORAN, AE ;
LESLIE, MD ;
LAING, JHE .
BRITISH JOURNAL OF CANCER, 1992, 65 (06) :870-878
[6]  
BERNSEN HJJ, 1997, UNPUB COMP ENDOTHELI
[7]   VASCULARITY AND PERFUSION OF HUMAN GLIOMAS XENOGRAFTED IN THE ATHYMIC NUDE-MOUSE [J].
BERNSEN, HJJA ;
RIJKEN, PFJW ;
OOSTENDORP, T ;
VANDERKOGEL, AJ .
BRITISH JOURNAL OF CANCER, 1995, 71 (04) :721-726
[8]   TUMOR HYPOXIA - THE PICTURE HAS CHANGED IN THE 1990S [J].
BROWN, JM ;
GIACCIA, AJ .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1994, 65 (01) :95-102
[9]  
BUSSINK J, 1995, IN VITRO CELL DEV-AN, V31, P547
[10]  
Chalkley HW, 1943, J NATL CANCER I, V4, P47