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PMID: 1677972 Published · ppublish English Journal Article Review

Modification of tumour blood flow--a review.

International journal of radiation biology ·Vol. 60 ·No. 1-2 ·1991-00-00 ·Pages 201-10

Peterson HI

Abstract

Tumour vascularization is based on two types of vessels, incorporated normal host tissue vessels and newly formed vessels, and is characterized by a wide heterogeneity. No adrenergic innervation has been related to newly formed tumour vessels but may still be found in incorporated normal vessels. In most studies vasoconstricting drugs were found to decrease tumour blood flow, while vasodilating drugs had no significant influence on tumour blood flow. From this it was concluded that the tumour vascular bed is normally in a state close to maximal dilatation, and this is supported by observations of hypoxia and local acidosis in tumour tissue. Some conflicting results have been reported with an increased tumour blood flow after administration of, for example, calcium channel blockers. Tumour blood modification is of interest in radiotherapy but also in tumour hyperthermia, where circulatory disturbances are explained on a multifactorial basis. Based on conflicting observations, with results varying with tumour-host systems studied and techniques for flow recording, it seems reasonable to concentrate further on methodological studies to develop clinically relevant techniques for tumour blood flow recording.

MeSH Terms
Anesthesia Blood Vessels/innervation,pathology Humans Hyperthermia, Induced Microcirculation/drug effects Microspheres Neoplasms/blood supply Vasoconstrictor Agents/pharmacology Vasodilator Agents/pharmacology
Chemicals
Vasoconstrictor Agents Vasodilator Agents
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Peterson H I
Department of Surgery, University of Göteborg, Sweden.
Article Info
Journal
International journal of radiation biology
Abbr.
Int J Radiat Biol
ISSN
0955-3002
Published
1991-00-00
Pages
201-10
Language
English
Region
England
NLM ID
8809243
Subset
IM
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