Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention  Susan G. Komen for the Cure-AACR Outstanding Investigator Award for Breast Cancer Research
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 Cell Growth & Differentiation

[Cancer Research 51, 5898-5902, November 1, 1991]
© 1991 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 Wilder, P. J.
Right arrow Articles by Rizzino, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wilder, P. J.
Right arrow Articles by Rizzino, A.

Effects of Transforming Growth Factor ß on the Anchorage-independent Growth of Murine Epithelial JB6 Cells1

Phillip J. Wilder and Angie Rizzino2

Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska 68198-6805

The work described in this paper demonstrates that transforming growth factor ß (TGF-ß) induces the soft agar growth of murine epidermal JB6 clone 41 (Cl 41) cells. In this regard, TGF-ß is more effective than either 12-O-tetradecanoylphorbol-13-acetate or epidermal growth factor. Together, TGF-ß1 and epidermal growth factor produce a greater stimulation of soft agar growth than either growth factor alone. In contrast, addition of TGF-ß1 and 12-O-tetradecanoylphorbol-13-acetate together does not stimulate soft agar growth beyond that produced by TGF-ß1 alone. Interestingly, retinoic acid inhibits the ability of all three factors to induce the anchorage-independent growth of Cl 40 cells. TGF-ß also exerts long-term effects on Cl 41 cells. This was determined by isolating TGF-ß-induced soft agar colonies and examining their dependence on TGF-ß. Five of the six anchorage-independent clones isolated after TGF-ß1 treatment were found to exhibit anchorage-independent growth in the absence of TGF-ß. In addition, these clones respond far more strongly to TGF-ß1 than do the parental Cl 41 cells in terms of both the numbers and the sizes of colonies formed in soft agar. The findings reported here are compatible with the proposal that TGF-ß mediates some effects of 12-O-tetradecanoylphorbol-13-acetate.

1 This work was supported by grants from the Council of Tobacco Research (2520) and the National Institute of Child Health and Development (HD 19837) and by core support grants from the National Cancer Institute (Laboratory Cancer Research Center Support Grant CA 36727) and the American Cancer Society (ACS SIG-16). P. J. W. was supported by NIH Training Grant T32 CA-09476.

2 To whom requests for reprints should be addressed, at Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, 600 South 42nd Street, Omaha, NE 68198-6805.

Received 6/ 4/91. Accepted 8/27/91.




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
C. Ma, J. Wang, and J. Luo
Exposure to Asphalt Fumes Activates Activator Protein-1 through the Phosphatidylinositol 3-Kinase/Akt Signaling Pathway in Mouse Epidermal Cells
J. Biol. Chem., November 7, 2003; 278(45): 44265 - 44272.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
R. M. Peterson, Q. Yu, I. Stamenkovic, and B. P. Toole
Perturbation of Hyaluronan Interactions by Soluble CD44 Inhibits Growth of Murine Mammary Carcinoma Cells in Ascites
Am. J. Pathol., June 1, 2000; 156(6): 2159 - 2167.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Huang, W.-Y. Ma, M. R. Young, N. Colburn, and Z. Dong
Shortage of mitogen-activated protein kinase is responsible for resistance to AP-1 transactivation and transformation in mouse JB6 cells
PNAS, January 6, 1998; 95(1): 156 - 161.
[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 Cell Growth & Differentiation
Copyright © 1991 by the American Association for Cancer Research.