Differences in the response of the microcirculation to hyperthermia in five different tumours

The response of the microcirculation in five different tumours, growing in ‘sandwich’ observation chambers in the back of the rat, to hyperthermia was investigated. The tumours investigated encompassed three human xenografted tumours, of which two were carcinomata of the colon and one of the lung, a...

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Published inEuropean journal of cancer & clinical oncology Vol. 25; no. 4; pp. 611 - 618
Main Authors Reinhold, H.S., van den Berg-Blok, A.E.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.04.1989
New York, NY Pergamon Press
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Abstract The response of the microcirculation in five different tumours, growing in ‘sandwich’ observation chambers in the back of the rat, to hyperthermia was investigated. The tumours investigated encompassed three human xenografted tumours, of which two were carcinomata of the colon and one of the lung, and two isologous rat tumours, the Rhabdomyosarcoma BA 1112 and a rat mammary carcinoma. It was concluded ( 1) that the various tumours required significantly different exposure times for inducing 50% stoppage of the tumour microcirculation ( st 50 ). This seems to indicate that differences in the characteristics of the tumour cells are more important for causing microcirculatory stoppage than is the sensitivity of the cells of the blood vessels. ( 2) An increase in surface (i.e. volume) was observed in all four tumours examined for this phenomenon. The rate of increase (usually 1–2% per hour at 42.5°C) was, however, significantly different between the various tumours. This rate was higher by higher exposure temperatures ( 43 and 43.5°C), but this was only investigated for the Rhabdomyosarcoma BA 1112. Extensive statistical analysis of this phenomenon of volume increase could not demonstrate a correlation with any of the circulation parameters. ( 3) The relative velocity of the erythrocytes in selected capillaries in the tumours decreases as a result of the hyperthermic treatment, and is probably related to the tumour-specific st 50 . ( 4) A human colon carcinoma xenograft, one of the tumours investigated, showed strong fluctuations in the parameter ‘erythrocyte velocity’. The appearance of such fluctuations did not seem to influence the heat-induced stoppage of the circulation. Probably the phenomenon of fluctuations in the velocities of the erythrocytes in the tumour capillaries is a tumour-specific phenomenon.
AbstractList The response of the microcirculation in five different tumours, growing in 'sandwich' observation chambers in the back of the rat, to hyperthermia was investigated. The tumours investigated encompassed three human xenografted tumours, of which two were carcinomata of the colon and one of the lung, and two isologous rat tumours, the Rhabdomyosarcoma BA1112 and a rat mammary carcinoma. It was concluded (1) that the various tumours required significantly different exposure times for inducing 50% stoppage of the tumour microcirculation (ST50). This seems to indicate that differences in the characteristics of the tumour cells are more important for causing microcirculatory stoppage than is the sensitivity of the cells of the blood vessels. (2) An increase in surface (i.e. volume) was observed in all four tumours examined for this phenomenon. The rate of increase (usually 1-2% per hour at 42.5 degrees C) was, however, significantly different between the various tumours. This rate was higher exposure temperatures (43 and 43.5 degrees C), but this was only investigated for the Rhabdomyosarcoma BA1112. Extensive statistical analysis of this phenomenon of volume increase could not demonstrate a correlation with any of the circulation parameters. (3) The relative velocity of the erythrocytes in selected capillaries in the tumours decreases as a result of the hyperthermic treatment, and is probably related to the tumour-specific ST50. (4) A human colon carcinoma xenograft, one of the tumours investigated, showed strong fluctuations in the parameter 'erythrocyte velocity'. The appearance of such fluctuations did not seem to influence the heat-induced stoppage of the circulation. Probably the phenomenon of fluctuations in the velocities of the erythrocytes in the tumour capillaries is a tumour-specific phenomenon.
The response of the microcirculation in five different tumours, growing in ‘sandwich’ observation chambers in the back of the rat, to hyperthermia was investigated. The tumours investigated encompassed three human xenografted tumours, of which two were carcinomata of the colon and one of the lung, and two isologous rat tumours, the Rhabdomyosarcoma BA 1112 and a rat mammary carcinoma. It was concluded ( 1) that the various tumours required significantly different exposure times for inducing 50% stoppage of the tumour microcirculation ( st 50 ). This seems to indicate that differences in the characteristics of the tumour cells are more important for causing microcirculatory stoppage than is the sensitivity of the cells of the blood vessels. ( 2) An increase in surface (i.e. volume) was observed in all four tumours examined for this phenomenon. The rate of increase (usually 1–2% per hour at 42.5°C) was, however, significantly different between the various tumours. This rate was higher by higher exposure temperatures ( 43 and 43.5°C), but this was only investigated for the Rhabdomyosarcoma BA 1112. Extensive statistical analysis of this phenomenon of volume increase could not demonstrate a correlation with any of the circulation parameters. ( 3) The relative velocity of the erythrocytes in selected capillaries in the tumours decreases as a result of the hyperthermic treatment, and is probably related to the tumour-specific st 50 . ( 4) A human colon carcinoma xenograft, one of the tumours investigated, showed strong fluctuations in the parameter ‘erythrocyte velocity’. The appearance of such fluctuations did not seem to influence the heat-induced stoppage of the circulation. Probably the phenomenon of fluctuations in the velocities of the erythrocytes in the tumour capillaries is a tumour-specific phenomenon.
Author van den Berg-Blok, A.E.
Reinhold, H.S.
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10.3109/02656738609012389
10.1016/0014-2964(79)90083-5
10.1007/978-3-642-82955-0_3
10.2307/3576582
10.1088/0031-9155/32/7/001
10.1016/0277-5379(83)90420-0
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Issue 4
Keywords Microcirculation
Vertebrata
Mammalia
Rat
Mouse
Rodentia
Various treatments
Tumor
Experimental study
Heterotransplantation
Experimental tumor
Induced hyperthermia
Language English
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Snippet The response of the microcirculation in five different tumours, growing in ‘sandwich’ observation chambers in the back of the rat, to hyperthermia was...
The response of the microcirculation in five different tumours, growing in 'sandwich' observation chambers in the back of the rat, to hyperthermia was...
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SubjectTerms Adenocarcinoma - blood supply
Adenocarcinoma - therapy
Animals
Biological and medical sciences
Blood Flow Velocity
Carcinoma, Small Cell - blood supply
Carcinoma, Small Cell - therapy
Colonic Neoplasms - blood supply
Colonic Neoplasms - therapy
Humans
Hyperthermia, Induced
Induced hyperthermia. Cryotherapy
Lung Neoplasms - blood supply
Lung Neoplasms - therapy
Mammary Neoplasms, Experimental - blood supply
Mammary Neoplasms, Experimental - therapy
Medical sciences
Microcirculation
Neoplasm Transplantation
Neoplasms, Experimental - blood supply
Rats
Rats, Inbred Strains
Rhabdomyosarcoma - blood supply
Rhabdomyosarcoma - therapy
Treatment with physical agents
Treatment. General aspects
Tumors
Title Differences in the response of the microcirculation to hyperthermia in five different tumours
URI https://dx.doi.org/10.1016/0277-5379(89)90194-6
https://www.ncbi.nlm.nih.gov/pubmed/2540985
https://search.proquest.com/docview/78980600
Volume 25
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