1967
DOI: 10.1097/00007890-196701000-00022
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Studies on hypophyseal isografts in mice. I. Biologic aspects

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Cited by 5 publications
(7 citation statements)
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“…This endogenous MTV is expressed in the C3Hf mice at later age and is linked to the late onset of mammary tumors in this strain (26). The incidence of mammary tumors in this C3Hf strain is dramatically increased in mice which have obtained a hypophyseal isograft (5). The 020 mouse strain seldom develops any mammary tumors.…”
Section: Resultsmentioning
confidence: 95%
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“…This endogenous MTV is expressed in the C3Hf mice at later age and is linked to the late onset of mammary tumors in this strain (26). The incidence of mammary tumors in this C3Hf strain is dramatically increased in mice which have obtained a hypophyseal isograft (5). The 020 mouse strain seldom develops any mammary tumors.…”
Section: Resultsmentioning
confidence: 95%
“…Another way of inducing mammary tumors in the low-mammary-tumor mouse strains is by implantation of multiple hypophyseal isografts in these mice (18). Prolactin is then continuously released, and the excessive amount of this lactogenic hormone causes high-mammary-tumor frequencies in almost all mouse strains (5,6).…”
mentioning
confidence: 99%
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“…As a rule, all experimental animals were kept in plastic cages (three mice per cage). Hormone treatment was carried out as described previously (Boot and Ropcke, 1966) as follows. Four hypophyseal isografts were implanted, two into each kidney of C3Hf females at an age of 6 to 8 weeks; one hypophysis each was implanted into the left kidney of castrated 0 2 0 and C57BL males at the age of 6 to 8 weeks, estrone (0.25 mgAiter) being added to the drinking water throughout the whole lifespan of the mouse, while 3 mg of progesterone was given subcutaneously once every week.…”
Section: Micementioning
confidence: 99%
“…However, pituitary isografts and systemic PRL treatment increased the development of spontaneous tumors in mice, and cooperated with chemical carcinogens to induce mammary tumors in the rat (Boot et al, 1962;Welsch and Nagasawa, 1977). When PRL À/À mice were crossed with transgenic mice expressing polyoma middle-T antigen driven by the MMTV promoter (PyVT mice), pituitary transplants decreased tumor latency and increased tumor growth rate (Vomachka et al, 2000).…”
Section: Introductionmentioning
confidence: 99%