Molecular biology of breast cancer metastasis Molecular expression of vascular markers by aggressive breast cancer cells
- 1. University of Iowa, Iowa City, Iowa (United States)
Description
During embryogenesis, the formation of primary vascular networks occurs via the processes of vasculogenesis and angiogenesis. In uveal melanoma, vasculogenic mimicry describes the 'embryonic-like' ability of aggressive, but not nonaggressive, tumor cells to form networks surrounding spheroids of tumor cells in three-dimensional culture; these recapitulate the patterned networks seen in patients' aggressive tumors and correlates with poor prognosis. The molecular profile of these aggressive tumor cells suggests that they have a deregulated genotype, capable of expressing vascular phenotypes. Similarly, the embryonic-like phenotype expressed by the aggressive human breast cancer cells is associated with their ability to express a variety of vascular markers. These studies may offer new insights for consideration in breast cancer diagnosis and therapeutic intervention strategies
Availability note (English)
Available from http://dx.doi.org/10.1186/bcr88; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC138664Additional details
Identifiers
Publishing Information
- Journal Title
- Breast Cancer Research (Print)
- Journal Volume
- 2
- Journal Issue
- 6
- Journal Page Range
- p. 417-422
- ISSN
- 1465-5411
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47007011
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- MAMMARY GLANDS; MOLECULAR BIOLOGY; PHENOTYPE; RECEPTORS; THREE-DIMENSIONAL CALCULATIONS; THROMBIN; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; BLOOD COAGULATION FACTORS; BODY; ENZYMES; GLANDS; HYDROLASES; MEMBRANE PROTEINS; ORGANIC COMPOUNDS; ORGANS; PEPTIDE HYDROLASES; PROTEINS; SERINE PROTEINASES
Optional Information
- Copyright
- Copyright (c) 2000 Current Science Ltd
- Notes
- PMCID: PMC138664; PUBLISHER-ID: bcr88; PMID: 11250735; OAI: oai:pubmedcentral.nih.gov:138664