Cancer Research Cancer Epigenetics  EMT and Cancer Progression and Treatment
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 53, 663-667, February 1, 1993]
© 1993 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 Medina, D.
Right arrow Articles by Schwartz, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Medina, D.
Right arrow Articles by Schwartz, M.

Morphological and Functional Properties of TM Preneoplastic Mammary Outgrowths1

Daniel Medina, Frances S. Kittrell, Yong-Jian Liu and Marlene Schwartz

Baylor College of Medicine, Department of Cell Biology, Houston, Texas 77030

The TM series of preneoplastic mammary outgrowth lines was derived from the transplantation of the FSK mammary cell lines into the cleared mammary fat pads of syngeneic female BALB/c mice. The tumor-producing capabilities of the 6 TM outgrowth lines varied from high (TM2, -4, -6) to low (TM9, -10) to nil (TM3). Outgrowth lines 2, 4, and 6 each segregated into sublines of high and low tumor potential. The majority of the outgrowth lines exhibited a moderate to dense alveolar hyperplasia typical of mouse mammary hyperplasias. The exceptions to this picture were lines TM2H and TM10 which exhibited a unique ductular morphology. The ductular morphology was not correlated with tumor potential of the outgrowth lines but was correlated with the expression of K6 and K14 keratins in luminal epithelial cells. In an examination of the growth and hormonal responsiveness properties of the TM outgrowth lines, the TM3 line stands as distinct from the other lines and from any other lines previously characterized in BALB/c mice. The TM3 line grew very slowly and failed to fill the fat pad by 12 months of age. At 12 months of age, the alveolar hyperplasia had regressed so that only bare ducts were present. The TM3 outgrowth was ovarian hormone dependent for growth and alveolar differentiation. TM3 outgrowth represents a minimally deviated mammary hyperplasia which has acquired the immortal phenotype but not the other phenotypic characteristics of mammary preneoplasias. This outgrowth line will be useful for examining the essential molecular changes important for the preneoplastic state, some of which are reported in an accompanying paper (D. Medina et al., Cancer Res., 53: 668–674, 1993).

1 Supported by National Cancer Institute Research Grant CA-47112.

Received 7/20/92. Accepted 11/19/92.




This article has been cited by other articles:


Home page
J. Cell Sci.Home page
D. Medina and F. Kittrell
Stroma is not a major target in DMBA-mediated tumorigenesis of mouse mammary preneoplasia
J. Cell Sci., January 1, 2005; 118(1): 123 - 127.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
G. Chakravarty, D. Hadsell, W. Buitrago, J. Settleman, and J. M. Rosen
p190-B RhoGAP Regulates Mammary Ductal Morphogenesis
Mol. Endocrinol., June 1, 2003; 17(6): 1054 - 1065.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
W. Jiang, Z. Zhu, N. Bhatia, R. Agarwal, and H. J. Thompson
Mechanisms of Energy Restriction: Effects of Corticosterone on Cell Growth, Cell Cycle Machinery, and Apoptosis
Cancer Res., September 15, 2002; 62(18): 5280 - 5287.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
Z. Zhu, W. Jiang, H. E. Ganther, and H. J. Thompson
Mechanisms of Cell Cycle Arrest by Methylseleninic Acid
Cancer Res., January 1, 2002; 62(1): 156 - 164.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
W. Shi and M. N. Gould
Induction of cytostasis in mammary carcinoma cells treated with the anticancer agent perillyl alcohol
Carcinogenesis, January 1, 2002; 23(1): 131 - 142.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. G. Bonnette and D. L. Hadsell
Targeted Disruption of the IGF-I Receptor Gene Decreases Cellular Proliferation in Mammary Terminal End Buds
Endocrinology, November 1, 2001; 142(11): 4937 - 4945.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
Y. Liu, H. Asch, and M. F. Kulesz-Martin
Functional Quantification of DNA-binding Proteins p53 and Estrogen Receptor in Cells and Tumor Tissues by DNA Affinity Immunoblotting
Cancer Res., July 1, 2001; 61(14): 5402 - 5406.
[Abstract] [Full Text] [PDF]


Home page
Cell Growth Differ.Home page
G. Chakravarty, D. Roy, M. Gonzales, J. Gay, A. Contreras, and J. M. Rosen
p190-B, a Rho-GTPase-activating Protein, Is Differentially Expressed in Terminal End Buds and Breast Cancer
Cell Growth Differ., July 1, 2000; 11(7): 343 - 354.
[Abstract] [Full Text]


Home page
Cancer Res.Home page
C. Ip, H. J. Thompson, Z. Zhu, and H. E. Ganther
In Vitro and in Vivo Studies of Methylseleninic Acid: Evidence That a Monomethylated Selenium Metabolite Is Critical for Cancer Chemoprevention
Cancer Res., June 1, 2000; 60(11): 2882 - 2886.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
P Schedin, R Strange, T Mitrenga, P Wolfe, and M Kaeck
Fibronectin fragments induce MMP activity in mouse mammary epithelial cells: evidence for a role in mammary tissue remodeling
J. Cell Sci., January 3, 2000; 113(5): 795 - 806.
[Abstract] [PDF]


Home page
CarcinogenesisHome page
S. G. Bonnette, F. S. Kittrell, L.C. Stephens, R. E. Meyn, and D. Medina
Interactions of apoptosis, proliferation and host age in the regression of the mouse mammary preneoplasia, TM3, carrying an unusual mutation in p53
Carcinogenesis, September 1, 1999; 20(9): 1715 - 1720.
[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 © 1993 by the American Association for Cancer Research.