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[Cancer Research 45, 6005-6009, December 1, 1985]
© 1985 American Association for Cancer Research

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Experimental Metastatic Ability of H-ras-transformed NIH3T3 Cells

Gregory P. Bondy1, Sylvia Wilson and Ann F. Chambers2

Ontario Cancer Foundation, London Clinic and Department of Radiation Oncology, University of Western Ontario, London, Ontario, Canada N6A 4G5

We have used a quantitative "experimental" metastasis assay in the embryonic chick, an immunodeficient host, to examine in vivo growth properties of ras oncogene-transformed NIH3T3 cells. We found that two independently derived populations of NIH3T3 cells that had been morphologically transformed with the T24 human H-ras oncogene were able to grow in vivo following i.v. injection. Nontransformed control NIH3T3 cells with normal morphology did not grow in this assay. Spontaneously arising morphological transformants from control NIH3T3 cell populations were also tested and did not grow in this assay. We conclude that the H-ras gene can confer experimental metastatic ability on nonmetastatic NIH3T3 cells, that the ras gene alters the cells in some way beyond in vitro morphological transformation, and thus that the in vitro transformation assay detects only part of the malignant phenotype of these cells.

1 Supported by a Terry Fox Training Centre Establishment Grant.

2 Supported by the National Cancer Institute of Canada and the Ontario Cancer Treatment and Research Foundation. To whom requests for reprints should be addressed.

Received 5/10/85. Revised 8/15/85. Accepted 8/20/85.







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
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1985 by the American Association for Cancer Research.