| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Molecular Endocrinology, Vol 8, 218-229, Copyright © 1994 by Endocrine Society
ARTICLES |
S Coleman-Krnacik and JM Rosen
Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.
Mammary gland development is dependent upon local regulatory factors as well as systemic hormones to mediate gland morphogenesis and associated mesenchymal-epithelial interactions. FGF-3 (int-2) has been implicated as an oncogenic growth factor produced locally in mouse mammary tumor virus-induced mammary tumorigenesis. The observation that FGF-3 is not expressed during normal mammary development as well as the high degree of cellular proliferation and angiogenesis that accompany mammary gland growth suggest roles for other FGF family members in this process. In this study, we have examined expression of FGF family members at various stages of mouse mammary growth and tumorigenesis. FGF-1, FGF-2, FGF-4, and FGF-7 were expressed during the ductal stage of mammary development. The majority of FGF-1 gene expression was in the luminal epithelial cells, whereas FGF-2 expression was in the mammary stroma and possibly the myoepithelial cells. The presence of mammary epithelium induced the expression of both FGF-2 and FGF-7 in the stroma. FGF-1 and FGF-2 expression declined during pregnancy and dropped again during lactation, but quantitative analysis showed a much more dramatic decrease in FGF-2 expression. FGF-7 transcripts were also detected during pregnancy and lactation, but an alternate transcript size was observed at these stages. FGF-1, FGF-2, and FGF-7 transcripts were detected in mammary preneoplasias, tumors, and immortal cell lines, but at levels less than those seen during normal mammary growth. These results support the hypothesis that FGF family members play a role in local regulation of mammary development. The differential spatial and temporal pattern of FGF-1, FGF-2 and FGF-7 gene expression indicate that they each have unique functions in the gland.
This article has been cited by other articles:
![]() |
X. Wang, C. Maltecca, R. Tal-Stein, E. Lipkin, and H. Khatib Association of Bovine Fibroblast Growth Factor 2 (FGF2) Gene with Milk Fat and Productive Life: An Example of the Ability of the Candidate Pathway Strategy to Identify Quantitative Trait Genes J Dairy Sci, June 1, 2008; 91(6): 2475 - 2480. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Jackson-Fisher, G. Bellinger, R. Ramabhadran, J. K. Morris, K.-F. Lee, and D. F. Stern ErbB2 is required for ductal morphogenesis of the mammary gland PNAS, December 7, 2004; 101(49): 17138 - 17143. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. S. W. Ngan, Z.-Q. Ma, S. S. Chua, F. J. DeMayo, and S. Y. Tsai Inducible expression of FGF-3 in mouse mammary gland PNAS, August 20, 2002; 99(17): 11187 - 11192. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. E. Welm, K. W. Freeman, M. Chen, A. Contreras, D. M. Spencer, and J. M. Rosen Inducible dimerization of FGFR1: development of a mouse model to analyze progressive transformation of the mammary gland J. Cell Biol., May 13, 2002; 157(4): 703 - 714. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hsieh, M. A. Johnson, N. M. Greenberg, and J. S. Richards Regulated Expression of Wnts and Frizzleds at Specific Stages of Follicular Development in the Rodent Ovary Endocrinology, March 1, 2002; 143(3): 898 - 908. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. Richards, D. L. Russell, S. Ochsner, M. Hsieh, K. H. Doyle, A. E. Falender, Y. K. Lo, and S. C. Sharma Novel Signaling Pathways That Control Ovarian Follicular Development, Ovulation, and Luteinization Recent Prog. Horm. Res., January 1, 2002; 57(1): 195 - 220. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Simian, Y. Hirai, M. Navre, Z. Werb, A. Lochter, and M. J. Bissell The interplay of matrix metalloproteinases, morphogens and growth factors is necessary for branching of mammary epithelial cells Development, August 15, 2001; 128(16): 3117 - 3131. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Lund, S. Bjorn, M. Sternlicht, B. Nielsen, H Solberg, P. Usher, R Osterby, I. Christensen, R. Stephens, T. Bugge, et al. Lactational competence and involution of the mouse mammary gland require plasminogen Development, January 10, 2000; 127(20): 4481 - 4492. [Abstract] [PDF] |
||||
![]() |
M. M. Richert and T. L. Wood The Insulin-Like Growth Factors (IGF) and IGF Type I Receptor during Postnatal Growth of the Murine Mammary Gland: Sites of Messenger Ribonucleic Acid Expression and Potential Functions Endocrinology, January 1, 1999; 140(1): 454 - 461. [Abstract] [Full Text] |
||||
![]() |
C. Lopez-Otin and E. P. Diamandis Breast and Prostate Cancer: An Analysis of Common Epidemiological, Genetic, and Biochemical Features Endocr. Rev., August 1, 1998; 19(4): 365 - 396. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. K. Pedchenko and W. T. Imagawa Mammogenic Hormones Differentially Modulate Keratinocyte Growth Factor (KGF)-Induced Proliferation and KGF Receptor Expression in Cultured Mouse Mammary Gland Epithelium Endocrinology, May 1, 1998; 139(5): 2519 - 2526. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Brisken, S. Park, T. Vass, J. P. Lydon, B. W. O'Malley, and R. A. Weinberg A paracrine role for the epithelial progesterone receptor in mammary gland development PNAS, April 28, 1998; 95(9): 5076 - 5081. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Rahmoune, H.-L. Chen, J. T. Gallagher, P. S. Rudland, and D. G. Fernig Interaction of Heparan Sulfate from Mammary Cells with Acidic Fibroblast Growth Factor (FGF) and Basic FGF. REGULATION OF THE ACTIVITY OF BASIC FGF BY HIGH AND LOW AFFINITY BINDING SITES IN HEPARAN SULFATE J. Biol. Chem., March 27, 1998; 273(13): 7303 - 7310. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Robinson and L Hennighausen Inhibins and activins regulate mammary epithelial cell differentiation through mesenchymal-epithelial interactions Development, January 7, 1997; 124(14): 2701 - 2708. [Abstract] [PDF] |
||||
![]() |
D Jackson, J Bresnick, I Rosewell, T Crafton, R Poulsom, G Stamp, and C Dickson Fibroblast growth factor receptor signalling has a role in lobuloalveolar development of the mammary gland J. Cell Sci., January 6, 1997; 110(11): 1261 - 1268. [Abstract] [PDF] |
||||
![]() |
D. Phippard, S. Weber-Hall, P. Sharpe, M. Naylor, H Jayatalake, R Maas, I Woo, D Roberts-Clark, P. Francis-West, Y. Liu, et al. Regulation of Msx-1, Msx-2, Bmp-2 and Bmp-4 during foetal and postnatal mammary gland development Development, January 9, 1996; 122(9): 2729 - 2737. [Abstract] [PDF] |
||||
![]() |
L. Lund, J Romer, N Thomasset, H Solberg, C Pyke, M. Bissell, K Dano, and Z Werb Two distinct phases of apoptosis in mammary gland involution: proteinase-independent and -dependent pathways Development, January 1, 1996; 122(1): 181 - 193. [Abstract] [PDF] |
||||
![]() |
M. Mathieu, E. Chatelain, D. Ornitz, J. Bresnick, I. Mason, P. Kiefer, and C. Dickson Receptor Binding and Mitogenic Properties of Mouse Fibroblast Growth Factor 3 J. Biol. Chem., October 13, 1995; 270(41): 24197 - 24203. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |