Published 2000 | Version v1
Journal article

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/PMC138664

Additional details

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