Development of the vascular system in the hamster malignant neurilemmoma☆,☆☆
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Cited by (88)
The role of mechanical host-tumour interactions in the collapse of tumour blood vessels and tumour growth dynamics
2006, Journal of Theoretical BiologyCitation Excerpt :It is interesting to consider that the oscillatory phase of growth is characterized by a process of complete collapse and re-opening of the penetrating blood vessels. This complete opening and closing of the tumour vasculature was observed by Eddy and Casarett (1972) who examined the vascular system in the hamster malignant neurilemmoma by allowing the tumours to grow between the two perspex plates of the transparent cheek pouch chamber. A general reduction in the blood flow occurred after about ten days of growth, which the investigators associated with the development of a tissue growth pressure within the rigid cheek pouch chamber.
A history of the study of solid tumour growth: The contribution of mathematical modelling
2004, Bulletin of Mathematical BiologyCitation Excerpt :A number of key experimental studies of tumour vascular collapse have also appeared in the literature over the past four or five decades—another aspect of tumour biology which is known to be detrimental to anti-cancer therapies (Jain, 1994). In the study by Eddy and Casarett (1972), for example, the development of a ‘tissue growth pressure’ around a hamster malignant neurilemmoma in a restrictive transparent cheek pouch chamber was sufficient to compress the weak-walled tumor capillary vessels. Further, in the experiments reported by Goldacre and Sylven (1962), a harmless green dye was injected into the tail veins of mice with transplanted tumours, giving rise to a deep green coloration of the whole animal with the exception of the brain (due to the blood–brain barrier) and the central regions of many of the solid tumours.
Changes in oxygenation status and blood flow in a rat tumor model by mild temperature hyperthermia
1999, International Journal of Radiation Oncology Biology PhysicsReperfusion of retinal nonperfusion by neovascular-vascular anastomosis in proliferative diabetic retinopathy
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This paper is based on work supported in part by the U.S. Public Health Service Grant CA-11051, and in part under contract with the U.S. Atomic Energy Commission at the University of Rochester Atomic Energy Project and has been assigned Report No. UR-3490-208.
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Presented in part at the 20th Annual Meeting of the Microcirculatory Society, 8–9 April 1972, Atlantic City, N.J.