Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2000-9-29
pubmed:abstractText
Tumor growth is partially dependent on angiogenesis, a process that relies on angiogenic factors. Tumorigenicity of cancer cells is thought to be associated with the production of various angiogenic factors that stimulate or inhibit the rate of endothelial cell migration and proliferation. However, the relative importance of specific individual factors originally studied in cancer cell lines has yet to be determined in vivo. In this study, we examined seven human glioma cell lines for dynamic changes of two major angiogenic factors, basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF), and for doubling time and tumorigenicity in nude mice. Various correlation studies demonstrated that in these glioma cell lines, VEGF expression correlated well with RBC density in tumor sections (r2 = 0.804) and with average tumor weight (r2 = 0.987). In contrast, bFGF expression in the observed glioma cell lines did not correlate with tumorigenicity (r2 = 0.001) or with VEGF expression (r2 = 0.255). Furthermore, there was no correlation between doubling time and tumorigenicity in these cell lines (r2 = 0.160). Taken together, these results suggest that VEGF plays a major role in glioma formation and that down-regulation of VEGF, rather than bFGF, would be a more effective choice for glioma gene therapy.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1078-0432
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2562-72
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:10873113-Animals, pubmed-meshheading:10873113-Blotting, Western, pubmed-meshheading:10873113-Brain Neoplasms, pubmed-meshheading:10873113-Cell Division, pubmed-meshheading:10873113-Culture Media, Conditioned, pubmed-meshheading:10873113-Down-Regulation, pubmed-meshheading:10873113-Endothelial Growth Factors, pubmed-meshheading:10873113-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:10873113-Fibroblast Growth Factor 2, pubmed-meshheading:10873113-Glioma, pubmed-meshheading:10873113-Humans, pubmed-meshheading:10873113-Immunohistochemistry, pubmed-meshheading:10873113-Lymphokines, pubmed-meshheading:10873113-Mice, pubmed-meshheading:10873113-Mice, Nude, pubmed-meshheading:10873113-Neoplasm Transplantation, pubmed-meshheading:10873113-Neovascularization, Pathologic, pubmed-meshheading:10873113-Time Factors, pubmed-meshheading:10873113-Tumor Cells, Cultured, pubmed-meshheading:10873113-Vascular Endothelial Growth Factor A, pubmed-meshheading:10873113-Vascular Endothelial Growth Factors
pubmed:year
2000
pubmed:articleTitle
The relevance of cell proliferation, vascular endothelial growth factor, and basic fibroblast growth factor production to angiogenesis and tumorigenicity in human glioma cell lines.
pubmed:affiliation
Department of Neuro-Oncology, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't