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Inhibition
of angiogenesis and tumor growth in the brain.
Suppression of endothelial cell
turnover by penicillamine and the depletion of copper, an angiogenic cofactor
Brem SS, Zagzag D, Tsanaclis AM, Gately S, Elkouby MP, Brien SE
Lady Davis Institute for Medical Research, Sir Mortimer B.
Davis-Jewish General Hospital, Montreal, Quebec, Canada
Microvascular proliferation, a hallmark of malignant brain tumors, represents an
attractive target of anticancer research, especially because of the quiescent
nonproliferative endothelium of the normal brain.
Cerebral neoplasms sequester copper, a trace metal that modulates
angiogenesis.
Using a rabbit brain tumor model, normocupremic animals developed large
vascularized VX2 carcinomas.
By contrast, small, circumscribed, relatively avascular tumors were found in the
brains of rabbits copper-depleted by diet and penicillamine treatment
(CDPT).
The CDPT rabbits showed a significant decrease in serum copper, copper staining
of tumor cell nuclei, microvascular density, the tumor volume, endothelial cell
turnover, and an increase in the vascular permeability (breakdown of the
blood-brain barrier), as well as peritumoral brain edema.
In non-tumor-bearing animals, CDPT did not alter the vascular permeability or
the brain water content.
CDPT also inhibited the intracerebral growth of the 9L gliosarcoma in F-344
rats, with a similar increase of the peritumoral vascular permeability and the
brain water content.
CDPT failed to inhibit tumor growth and the vascularization of the VX2 carcinoma
in the thigh muscle or the metastases to the lung, findings that may reflect
regional differences in the responsiveness of the endothelium, the distribution
of copper, or the activity of cuproenzymes.
Metabolic and pharmacologic withdrawal of copper suppresses intracerebral tumor
angiogenesis; angiosuppression is a novel biologic response modifier for the in
situ control of tumor growth in the brain.
PMID: 1700617 [PubMed - indexed for MEDLINE]
Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1700617&dopt=Abstract
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