Cancer Research  Translational Medicine Conference in Israel
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 47, 5316-5322, October 15, 1987]
© 1987 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 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 Ethier, S. P.
Right arrow Articles by Cundiff, K. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ethier, S. P.
Right arrow Articles by Cundiff, K. C.

Importance of Extended Growth Potential and Growth Factor Independence on in Vivo Neoplastic Potential of Primary Rat Mammary Carcinoma Cells1

S. P. Ethier2 and K. C. Cundiff

Breast Cancer Research Program, The Michigan Cancer Foundation, Detroit, Michigan 48201

Recently developed culture systems that allow extended growth of normal rat mammary epithelial (RME) cells were used to directly compare the proliferative potentials and growth factor requirements of primary normal and primary neoplastic rat mammary cells. RME cells were obtained from 45- to 55-day-old inbred female Lew rats and rat mammary tumor (RMT) cells from 7,12-dimethylbenz(a)anthracene- or N-nitrosomethylurea-induced mammary carcinomas. To compare the proliferative lifespan of RME and RMT cells, colony forming efficiencies were determined after consecutive passages over a 70-day culture period. Whereas the proliferative potential of RME cells declined with time in culture, RMT cells from five separate mammary carcinomas had colony forming efficiencies that increased with serial passage. By the end of the 70-day culture period, colony forming efficiencies for RMT cells were 100- to 1000-fold higher than those for RME cells. To compare the growth factor requirements for RME and RMT cells, a serum-free culture medium that supports RME cell growth was used and the influence of specific growth factors was examined by deletion experiments. Cells from 5 of 18 primary mammary carcinomas exhibited requirements for insulin, epidermal growth factor, and cholera toxin identical to those of RME cells. In contrast, cells from 9 of 18 tumors expressed independence of one, two, or all three of these factors for growth in serum-free culture. To examine the in vivo growth potential of primary RMT cells, samples of the cell suspensions used to initiate primary cultures were transplanted into the interscapular white fat pads of syngeneic female recipients. Transplantation of cells from growth factor dependent tumors yielded nonneoplastic mammary outgrowths. In contrast, transplantation of growth factor independent tumor cells yielded grossly visible tumors in 100% of the recipients within 4 weeks of transplantation. Thus, our results indicate that cells from all primary mammary carcinomas have dramatically enhanced growth potential in long-term culture relative to RME cells. Furthermore, a subset of these tumors are also independent of growth factors required by RME cells, and expression of growth factor independence is associated with high neoplastic potential in vivo.

1 This report from the A. Alfred Taubman Facility for Environmental Carcinogenesis Research was supported by USPHS grants CA40064 and RR-85529 and by an institutional grant from the United Foundation of Metropolitan Detroit.

2 To whom requests for reprints should be addressed.

Received 3/24/87. Revised 7/22/87. Accepted 7/24/87.




This article has been cited by other articles:


Home page
Cancer Res.Home page
M. Tatsumi, Y. Nakamoto, B. Traughber, L. T. Marshall, J.-F. H. Geschwind, and R. L. Wahl
Initial Experience in Small Animal Tumor Imaging with a Clinical Positron Emission Tomography/Computed Tomography Scanner Using 2-[F-18]Fluoro-2-deoxy-D-glucose
Cancer Res., October 1, 2003; 63(19): 6252 - 6257.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
K. M. W. Ignatoski, A. J. LaPointe, E. H. Radany, and S. P. Ethier
erbB-2 Overexpression in Human Mammary Epithelial Cells Confers Growth Factor Independence
Endocrinology, August 1, 1999; 140(8): 3615 - 3622.
[Abstract] [Full Text]




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 © 1987 by the American Association for Cancer Research.