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[Cancer Research 52, 1764-1769, April 1, 1992]
© 1992 American Association for Cancer Research

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Retention of Cellular Radiation Sensitivity in Cell and Xenograft Lines Established from Human Melanoma Surgical Specimens1

Einar K. Rofstad2

Institute for Cancer Research and the Norwegian Cancer Society, Norwegian Radium Hospital, Montebello, 0310 Oslo 3, Norway

Six human melanoma xenograft lines have been established in athymic mice from metastatic lesions in six different patients. Permanent cell lines in monolayer culture have been established from four of the xenograft lines. The cellular radiation sensitivity of the donor patients' tumors, the xenograft lines, and the cell lines were measured in vitro. The Courtenay soft agar colony assay was used for the donor patients' tumors, and a conventional plastic surface colony assay was used for the cell lines, whereas both assays were used for the xenograft lines. The cell survival data were analyzed using the multitarget single-hit as well as the linear-quadratic model. The donor patients' tumors differed considerably in cellular radiation sensitivity (the D0 ranged from 0.85 ± 0.08 to 1.17 ± 0.09 Gy, the {alpha} from 0.25 ± 0.06 to 0.87 ± 0.14 Gy–1, and the surviving fraction at 2.0 Gy from 0.15 ± 0.04 to 0.50 ± 0.06). The xenograft lines showed similar survival curves in soft agar and on the plastic surface, and the survival curves of a xenograft line and the corresponding cell line were not significantly different. These survival curves were not significantly different from those of the donor patients' tumors, regardless of which survival curve parameter was considered, i.e., the cellular radiation sensitivity of the donor patients' tumors was retained in the cell and xenograft lines. Moreover, the cell and xenograft lines have growth properties in vitro and in vivo that render a wide variety of experiments possible. Consequently, they show great promise for future studies of human tumor radiation biology.

1 Financial support was received from the Norwegian Cancer Society.

2 To whom requests for reprints should be addressed, at Department of Biophysics, Institute for Cancer Research, Norwegian Radium Hospital, Montebello, 0310 Oslo 3, Norway.

Received 10/ 7/91. Accepted 1/15/92.




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E. K. Rofstad, K. Henriksen, K. Galappathi, and B. Mathiesen
Antiangiogenic Treatment with Thrombospondin-1 Enhances Primary Tumor Radiation Response and Prevents Growth of Dormant Pulmonary Micrometastases after Curative Radiation Therapy in Human Melanoma Xenografts
Cancer Res., July 15, 2003; 63(14): 4055 - 4061.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1992 by the American Association for Cancer Research.