Cancer Research Annual Meeting 2010  Jordan
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

[Cancer Research 39, 4767-4771, December 1, 1979]
© 1979 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lotan, R.
Right arrow Articles by Nicolson, G. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lotan, R.
Right arrow Articles by Nicolson, G. L.

Heterogeneity in Growth Inhibition by ß-trans-Retinoic Acid of Metastatic B16 Melanoma Clones and in Vivo-selected Cell Variant Lines1

Reuben Lotan2 and Garth L. Nicolson

Department of Developmental and Cell Biology, School of Biological Sciences (R. L., G. L. N.], and Department of Physiology, College of Medicine [G. L. N.], University of California, Irvine, California 92717

A malignant B16 melanoma parental cell line, four unselected clones derived from this line which possess varying lung colonization potentials (clones 9 and 14 > parental B16 > clones 12 and 15), four variant cell lines selected in vivo for increased ability to colonize preferentially lungs (B16-F10 > B16-F1, parental B16), brain (B16-B10n > B16-F1, parental B16), or ovaries (B16-O10 > B16-F1, parental B16), and a line selected in vitro for resistance to lymphocyte cytotoxicity (B16-F10Lr-6) have been examined in culture for their susceptibilities to growth inhibition by retinoic acid. The proliferation of all clones and cell lines was inhibited in the presence of noncytotoxic concentrations of retinoic acid (10–5 and 10–6 M); however, the extent of inhibition varied significantly. The parental B16 line and parental clone 14, as well as the in vivo-selected variant cell lines B16-F1 and B16-B10n, were extremely sensitive to retinoic acid, and their growth was inhibited by 75 to 90% after a 5-day incubation in the presence of 10–5 M retinoic acid. Under similar conditions, the growth of parental clones 9, 12, and 15 and of selected cell lines B16-F10, B16-F10Lr-6, and B16-O10 was inhibited only moderately (40 to 60%). A more striking difference in sensitivity was observed when cells were exposed to a low retinoic acid concentration (10–9 M). While the parental B16 line and B16-F1 were inhibited by nearly 40%, parental clones 12 and 14 and selected cell line B16-F10Lr-6 were inhibited by about 20%, and parental clones 9 and 15 and lines B16-B10n, B16-O10, and B16-F10 were not significantly affected (0 to 10% inhibition). These results demonstrate that the parental B16 melanoma line is heterogeneous with respect to sensitivity to retinoic acid and includes some cell variants with reduced susceptibility to the drug.

1 Supported by USPHS Grants R01-CA-22823 and R01-CA-15122 and Contract N01-CB-74153 from the National Cancer Institute.

2 Recipient of Lievre Senior Fellowship D-295 of the American Cancer Society, California Division, Inc. To whom requests for reprints should be addressed.

Received 10/ 5/78. Accepted 8/21/79.




This article has been cited by other articles:


Home page
ScienceHome page
G. Nicolson and S. Custead
Tumor metastasis is not due to adaptation of cells to a new organ environment
Science, January 8, 1982; 215(4529): 176 - 178.
[Abstract] [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 © 1979 by the American Association for Cancer Research.