TY - JOUR
T1 - Vascular density in melanoma xenografts correlates with vascular permeability factor expression but not with metastatic potential
AU - Westphal, J. R.
AU - Van't Hullenaar, R. G.M.
AU - Van der Laak, J. A.W.M.
AU - Cornelissen, I. M.H.A.
AU - Schalkwijk, L. J.M.
AU - Van Muijen, G. N.P.
AU - Wesseling, P.
AU - De Wilde, P. C.M.
AU - Ruiter, D. J.
AU - De Waal, R. M.W.
N1 - Funding Information:
The authors wish to thank Bert Smeets and Willy Nillesen (Department of Human Genetics, University Hospital Nijmegen, Nijmegen) for performing CA repeat analysis, Coos Diepenbroek and co-workers for excellent histological analysis, and Dr A Hamann and Dr A Vecchi for providing the 9F1 hybridoma and the MEC7.46 antibody respectively. This work was supported by the Dutch Cancer Society (Grant NUKC 92-36).
PY - 1997
Y1 - 1997
N2 - We studied the relation between tumour vascular density and tumour growth rate, metastatic incidence and vascular permeability factor (VPF) mRNA levels in a human xenograft model described previously. Vascular density was determined by automated image analysis. Xenografts derived from cell lines BLM and MV3 showed the highest mean vascular density (MVD), the highest in vivo growth rate, high VPF mRNA levels and rapid development of lung metastases. Xenografts of cell lines M14, Mel57 and MV1 showed a significantly lower degree of vascularization, lower in vivo growth rates and lower levels of VPF mRNA, but formed lung metastases with a similar incidence as those of BLM and MV3. Xenografts from cell line 1F6 did not form lung metastases, whereas tumours derived from a spontaneous mutant of 1F6, designated 1F6m, gave rise to lung metastases to the same extent as Mel57, M14 and MV1 tumours. MVD values in 1F6 and 1F6m xenografts, VPF mRNA levels and in vivo growth rates of 1F6 and 1F6m xenografts, however, were similar. In conclusion, in the melanoma xenograft model vascular density is correlated with in vivo growth rate and with in vitro VPF mRNA levels, but not with the ability to metastasize.
AB - We studied the relation between tumour vascular density and tumour growth rate, metastatic incidence and vascular permeability factor (VPF) mRNA levels in a human xenograft model described previously. Vascular density was determined by automated image analysis. Xenografts derived from cell lines BLM and MV3 showed the highest mean vascular density (MVD), the highest in vivo growth rate, high VPF mRNA levels and rapid development of lung metastases. Xenografts of cell lines M14, Mel57 and MV1 showed a significantly lower degree of vascularization, lower in vivo growth rates and lower levels of VPF mRNA, but formed lung metastases with a similar incidence as those of BLM and MV3. Xenografts from cell line 1F6 did not form lung metastases, whereas tumours derived from a spontaneous mutant of 1F6, designated 1F6m, gave rise to lung metastases to the same extent as Mel57, M14 and MV1 tumours. MVD values in 1F6 and 1F6m xenografts, VPF mRNA levels and in vivo growth rates of 1F6 and 1F6m xenografts, however, were similar. In conclusion, in the melanoma xenograft model vascular density is correlated with in vivo growth rate and with in vitro VPF mRNA levels, but not with the ability to metastasize.
KW - Angiogenesis
KW - Melanoma
KW - Metastasis
KW - Vascular permeability factor
KW - Xenograft
UR - http://www.scopus.com/inward/record.url?scp=8544221117&partnerID=8YFLogxK
U2 - 10.1038/bjc.1997.427
DO - 10.1038/bjc.1997.427
M3 - Article
C2 - 9303353
AN - SCOPUS:8544221117
SN - 0007-0920
VL - 76
SP - 561
EP - 570
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 5
ER -