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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 14 (1986), S. 113-117 
    ISSN: 1434-0879
    Keywords: R3327H prostatic carcinoma ; Blood supply ; Testosterone ; Oestradiol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Copenhagen x Fischer F1 rats were implanted with Dunning R3327H prostatic adenocarcinoma and studied over a period of three weeks. The tumour volumes in intact and testosterone supplemented castrated rats showed parallel increases. After castration alone the tumour volumes decreased. Treatment of castrates with oestradiol and testosterone combined produced an arrest of tumour growth, suggesting that oestradiol had a direct inhibitory effect on tumour growth. Blood flow in tumours was measured using the microsphere technique. In intact rats, tumour blood flow per unit of weight decreased with increasing weight of tumours and blood flow in peripheral parts was higher than in central parts of large tumours. Oestradiol in combination with testosterone increased tumour blood flow.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 15 (1987), S. 169-172 
    ISSN: 1434-0879
    Keywords: Morphometry ; Oestradiol ; R3327H prostatic carcinoma ; Testosterone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Male Copenhagen x Fischer F1 rats were implanted with Dunning R3327H prostatic carcinoma, castrated when the tumours became palpable and were then treated with testosterone, testosterone in combination with oestradiol or oestradiol alone for four weeks. Treatment with oestradiol produced the smallest tumours. The testosteronestimulated growth of tumours was inhibited by oestradiol. The adenocarcinoma was moderately to well-differentiated. Morphometric analysis of the composition of the tumours showed that oestradiol stimulated tumour stroma and inhibited glandular epithelium. These effects were produced concomitantly with decreased overall tumour growth. Testosterone stimulated all cell types of the tumour.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 118 (1992), S. 30-34 
    ISSN: 1432-1335
    Keywords: Morphometry ; Oestradiol ; R3327 prostatic adenocarcinoma ; Testosterone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present study was undertaken to investigate to what extent the oestrogen-induced effects on growth and morphology of the Dunning R3327 rat prostatic adenocarcinoma are dose-dependent. Castrated and testosterone-supplemented rats were used in order to study effects of increasing doses of oestrogens on the tumour. It was found that the lowest dose of oestradiol-17β that reduced the overall growth, the volume density of the epithelium and epithelial cell area in Dunning R3327 prostatic tumours is 10 μg given as daily injections. Higher oestrogen doses (50 μg, 200 μg, and 500 μg), in addition to reducing the volume of tumour epithelium, also induced an increase of the volume density of tumour stroma. The area of stroma cell nuclei was increased by 50 μg and 200 μg oestradiol-17β. These observation, may indicate that the lowest effective oestrogen dose is different in the epithelium and stroma of Dunning tumours and that large doses of oestrogen stimulate the stromal compartment. This stimulatory effect did not influence the inhibitory effects seen on the overall growth of the tumour and on the tumor epithelium.
    Type of Medium: Electronic Resource
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