2009
DOI: 10.1016/j.jsbmb.2009.09.007
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Effect of testosterone on E1S-sulfatase activity in non-malignant and cancerous breast cells in vitro

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Cited by 6 publications
(7 citation statements)
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“…By "direct" incubation, we believe to obtain more valid information about regulation of the selected compounds at the level of the enzyme's catalytic activity. Our findings in brain are in agreement with previous studies in malignant breast cells and normal mammary gland, demonstrating an inhibitory effect on STS activity after "direct" incubation by iCR [18], E2 [15], T [19] and Org4094 [15], respectively.…”
Section: Discussionsupporting
confidence: 93%
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“…By "direct" incubation, we believe to obtain more valid information about regulation of the selected compounds at the level of the enzyme's catalytic activity. Our findings in brain are in agreement with previous studies in malignant breast cells and normal mammary gland, demonstrating an inhibitory effect on STS activity after "direct" incubation by iCR [18], E2 [15], T [19] and Org4094 [15], respectively.…”
Section: Discussionsupporting
confidence: 93%
“…Our results contribute to our previous work showing that local STS activity can be modulated by exogenous steroids and black cohosh [15,18,19,34] -also in brain (this study). This might be one explanation as to how those compounds frequently used in menopausal women may affect cognition.…”
Section: Discussionsupporting
confidence: 87%
“…However, the extent of enzyme inhibition was tissuedependent, and mammary 17bHSD1 seemed to be more sensitive to co-incubated testosterone although this difference was not significant. Apart from 17bHSD1, previous studies found an inhibitory effect of testosterone on mammary aromatase 43 , and STS activity 23 , respectively. These in vitro findings support the hypothesis of an anti-estrogenic effect of testosterone on the mammary gland, which has previously been postulated [44][45][46] .…”
Section: Discussionmentioning
confidence: 92%
“…For the PA, the conversion of the co-substrate NADH to NAD+ in the presence of the substrate E1 was used to determine E2 formation 35 . Therefore, 60 ml enzyme solution in assay buffer (0.2 M Tris-HCl, 0.1 M Na 2 HPO 4 , pH 6.9) were mixed with 30 ml substrate (381 mg/ml E1 in 95% ethanol), and 60 ml NADH (1 mg/ml) in assay buffer in the presence or absence of the following substances 23,31 ( Figure 1):…”
Section: Human Placenta and Mammary Glandmentioning
confidence: 99%
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