Journal Article

Smad4/DPC4-Mediated Tumor Suppression through Suppression of Angiogenesis

Sipos, Bence, Luttges, Jutta, Graeven, Ulrich, Hahn, Stephan A., Kloppel, Gunter, Schmiegel, Wolff, Volpert, Olga V., Schwarte-Waldhoff, Irmgard, Bouck, Noel P., Klein-Scory, Susanne, Eilert-Micus, Christina, Hintelmann, Annette

2000

Overview

Smad4/DPC4 (deleted in pancreatic carcinoma, locus 4) is a tumor suppressor gene lost at high frequency in cancers of the pancreas and other gastrointestinal organs. Smad4 encodes a key intracellular messenger in the transforming growth factor β (TGF-β ) signaling cascade. TGF-β is a potent inhibitor of the growth of epithelial cells; thus, it has been assumed that loss of Smad4 during tumor progression relieves this inhibition. Herein, we show that restoration of Smad4 to human pancreatic carcinoma cells suppressed tumor formation in vivo, yet it did not restore sensitivity to TGF-β . Rather, Smad4 restoration influenced angiogenesis, decreasing expression of vascular endothelial growth factor and increasing expression of thrombospondin-1. In contrast to the parental cell line and to control transfectants that produced rapidly growing tumors in vivo, Smad4 revertants induced small nonprogressive tumors with reduced vascular density. These data define the control of an angiogenic switch as an alternative, previously unknown mechanism of tumor suppression for Smad4 and identify the angiogenic mediators vascular endothelial growth factor and thrombospondin-1 as key target genes.

• Publisher: National Academy of Sciences of the United States of America,National Acad Sciences,National Academy of Sciences,The National Academy of Sciences
• Subject: Angiogenesis / Animals / Antibodies / Antineoplastic Agents - metabolism / Biological Sciences / Carcinoma / Cell culture techniques / Cell Division - drug effects / Cell growth / Cell lines / Cell Movement / DNA-Binding Proteins - genetics / DNA-Binding Proteins - metabolism / Drug Resistance, Neoplasm / Endothelial cells / Endothelial Growth Factors - genetics / Endothelial Growth Factors - metabolism / Endothelium, Vascular - metabolism / Endothelium, Vascular - pathology / Epithelial cells / Fibroblast Growth Factor 2 - pharmacology / Genes, Tumor Suppressor - genetics / Genetics / Humans / Lymphokines - genetics / Lymphokines - metabolism / Medical research / Mice / Mice, Nude / Neoplasm Transplantation / Neovascularization, Pathologic / Pancreatic Neoplasms - blood supply / Pancreatic Neoplasms - genetics / Pancreatic Neoplasms - metabolism / Pancreatic Neoplasms - pathology / Receptors, Transforming Growth Factor beta - metabolism / RNA, Messenger - genetics / RNA, Messenger - metabolism / Signal Transduction - drug effects / Smad4 Protein / Thrombospondin 1 - genetics / Thrombospondin 1 - metabolism / thrombospondin-1 / Trans-Activators - genetics / Trans-Activators - metabolism / Transfection / Transforming Growth Factor beta - pharmacology / Tumor cell line / Tumor Cells, Cultured / Tumors / Vascular Endothelial Growth Factor A / Vascular Endothelial Growth Factors