A novel gene expression profile in lymphatics associated with tumor growth and nodal metastasis.

Clasper S., Royston D., Baban D., Cao Y., Ewers S., Butz S., Vestweber D., Jackson DG.

Invasion of lymphatic vessels is a key step in the metastasis of primary tumors to draining lymph nodes. Although the process is enhanced by tumor lymphangiogenesis, it is unclear whether this is a consequence of increased lymphatic vessel number, altered lymphatic vessel properties, or both. Here we have addressed the question by comparing the RNA profiles of primary lymphatic endothelial cells (LEC) isolated from the vasculature of normal tissue and from highly metastatic T-241/vascular endothelial growth factor (VEGF)-C fibrosarcomas implanted in C57BL/6 mice. Our findings reveal significant differences in expression of some 792 genes (i.e., >or=2-fold up- or down-regulated, P

DOI

10.1158/0008-5472.CAN-07-6506

Type

Journal article

Journal

Cancer Res

Publication Date

15/09/2008

Volume

68

Pages

7293 - 7303

Keywords

Animals, Cell Adhesion Molecules, Cell Growth Processes, Endoglin, Endothelial Cells, Fibrosarcoma, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Intracellular Signaling Peptides and Proteins, Junctional Adhesion Molecules, Lymph Nodes, Lymphatic Metastasis, Mice, Mice, Inbred C57BL, Neoplasms, Neovascularization, Pathologic, Oligonucleotide Array Sequence Analysis, Receptors, Leptin, Transforming Growth Factor beta, Vascular Endothelial Growth Factor C

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