IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Woodward, J. K. L.
Right arrow Articles by Sisley, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Woodward, J. K. L.
Right arrow Articles by Sisley, K.
(Investigative Ophthalmology and Visual Science. 2002;43:3144-3152.)
© 2002 by The Association for Research in Vision and Ophthalmology, Inc.

Stimulation and Inhibition of Uveal Melanoma Invasion by HGF, GRO, IL-1{alpha} and TGF-ß

Julia K. L. Woodward1,2, Shona R. Elshaw2,3, Anna K. Murray4, Carmel E. Nichols1, Neil Cross4, David Laws5, Ian G. Rennie1 and Karen Sisley1

1 From the Academic Unit of Ophthalmology and Orthoptics, University of Sheffield, Royal Hallamshire Hospital, the 4 Institute for Cancer Studies, University of Sheffield Medical School, and the 5 Department of Probability and Statistics, University of Sheffield, Sheffield, United Kingdom; and the 3 Division of Therapeutics, School of Medical and Surgical Sciences, University of Nottingham, Queens Medical Centre, Nottingham, United Kingdom.

PURPOSE. To investigate potential factors involved in uveal melanoma migration and invasion in vitro.

METHODS. Using a microchemotaxis chamber, the effects were studied of a range of stimulators and inhibitors on a series of 10 primary uveal melanomas and 2 uveal melanoma cell lines, by assessing invasion through an 8-µm pore membrane, precoated with an extracellular matrix solution. In addition, invasion in response to the effect of cells and conditioned media derived from the liver and other tissues was studied for one uveal melanoma culture, by using double-chambered wells, and invasion was assessed through an 8-µm pore membrane, precoated with synthetic extracellular matrix. In all instances, invading cells were counted under x400 magnification on the lower surface of the membrane. Levels of invasion were correlated with histopathologic markers of prognosis.

RESULTS. Conditioned media and cells derived from other tissues, including the liver, increased cellular invasion of the uveal melanoma cell line studied. For specific regulators, maximum stimulation of invasion was induced by hepatic growth factor (HGF), growth-related oncogene (GRO), and macrophage inflammatory protein (MIP)-1ß, whereas significant inhibition was induced by IL-1{alpha}, TGF-ß1, and TGF-ß2.

CONCLUSIONS. The primary site of metastasis in patients with uveal melanoma is the liver. For the degree of site specificity commonly seen, regulators involved in the process may be expressed at the secondary sites, promoting adhesion, migration, invasion, and proliferation of tumor cells. HGF, GRO, MIP-1ß, IL-1{alpha}, TGF-ß1, and TGF-ß2 may play a significant role in regulating invasion of uveal melanoma cells.




This article has been cited by other articles:


Home page
Br J OphthalmolHome page
H S Mudhar, E Saunders, P Rundle, I G Rennie, and K Sisley
The in vivo modulatory effects of an anterior-chamber microenvironment on uveal melanoma
Br J Ophthalmol, April 1, 2009; 93(4): 535 - 540.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
S. Bakalian, J.-C. Marshall, P. Logan, D. Faingold, S. Maloney, S. Di Cesare, C. Martins, B. F. Fernandes, and M. N. Burnier Jr.
Molecular Pathways Mediating Liver Metastasis in Patients with Uveal Melanoma
Clin. Cancer Res., February 15, 2008; 14(4): 951 - 956.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
M. Ye, D. Hu, L. Tu, X. Zhou, F. Lu, B. Wen, W. Wu, Y. Lin, Z. Zhou, and J. Qu
Involvement of PI3K/Akt Signaling Pathway in Hepatocyte Growth Factor-Induced Migration of Uveal Melanoma Cells
Invest. Ophthalmol. Vis. Sci., February 1, 2008; 49(2): 497 - 504.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
D. Faingold, J.-C. Marshall, E. Antecka, S. Di Cesare, A. N. Odashiro, S. Bakalian, B. F. Fernandes, and M. N. Burnier Jr.
Immune Expression and Inhibition of Heat Shock Protein 90 in Uveal Melanoma
Clin. Cancer Res., February 1, 2008; 14(3): 847 - 855.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
H. Torisu-Itakura, J. H. Lee, R. P. Scheri, Y. Huynh, X. Ye, R. Essner, and D. L. Morton
Molecular Characterization of Inflammatory Genes in Sentinel and Nonsentinel Nodes in Melanoma
Clin. Cancer Res., June 1, 2007; 13(11): 3125 - 3132.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
D.-S. Son and K. F. Roby
Interleukin-1{alpha}-Induced Chemokines in Mouse Granulosa Cells: Impact on Keratinocyte Chemoattractant Chemokine, a CXC Subfamily
Mol. Endocrinol., November 1, 2006; 20(11): 2999 - 3013.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
J. K. L. Woodward, I. G. Rennie, J. L. Burn, and K. Sisley
A Potential Role for TGF{beta} in the Regulation of Uveal Melanoma Adhesive Interactions with the Hepatic Endothelium
Invest. Ophthalmol. Vis. Sci., October 1, 2005; 46(10): 3473 - 3477.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
Y. Ren, B. Cao, S. Law, Y. Xie, P. Y. Lee, L. Cheung, Y. Chen, X. Huang, H. M. Chan, P. Zhao, et al.
Hepatocyte Growth Factor Promotes Cancer Cell Migration and Angiogenic Factors Expression: A Prognostic Marker of Human Esophageal Squamous Cell Carcinomas
Clin. Cancer Res., September 1, 2005; 11(17): 6190 - 6197.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the Association for Research in Vision and Ophthalmology