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1.
Water Res ; 36(13): 3183-92, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12188114

ABSTRACT

Cylindrospermopsis raciborskii, a potentially toxic blooming cyanobacterium (blue-green alga), responsible for public health problems in Australia, was identified in France in 1994 in a shallow pond south of Paris. A program monitoring the occurrence of C. raciborskii in this pond was conducted from July 1998 to October 1999. The phytoplankton assemblages were studied, and limnological parameters (water temperature, dissolved oxygen, pH, conductivity, and dissolved inorganic nutrients) were measured. By multivariate analysis (principal component analysis), we showed that sufficiently high temperatures to allow the germination of akinetes, relatively low nutrient concentrations (soluble reactive phosphorus with a mean concentration of 1 microM and nitrate between 0 and 5 microM, except in February 1999 (21 microM)) and a characteristic high and constant sulfate concentration (8981+/-471 microM) seemed to be the main factors involved in the proliferation of C. raciborskii in the "Francs-Pêcheurs" (FP) pond. In the light of these findings and of bibliographic data, C. raciborskii would seem to be characterized by good adaptability, but also by low competitiveness with other phytoplanktonic species in the temperate study area.


Subject(s)
Cyanobacteria , Eutrophication , Adaptation, Physiological , Environmental Monitoring , France , Nitrates , Phosphorus , Population Dynamics , Temperature , Water Microbiology
2.
Cancer Res ; 61(10): 3942-8, 2001 May 15.
Article in English | MEDLINE | ID: mdl-11358810

ABSTRACT

Dioxin and pesticides with xenoestrogenic activity are environmental contaminants that are suspected of promoting human diseases such as cancers. However, few studies have addressed the molecular consequences of a combination of these contaminants, a situation that is likely to occur in the environment. We investigated the effects of natural and xenoestrogens on basal and 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced cytochrome P450 (CYP) 1A1 and 1B1. The CYP1B1/1A1 ratio is a critical determinant of the metabolism and toxicity of estradiol in mammary cells. Here we show that in MCF-7 cells, 17beta-estradiol and alpha-endosulfan can repress whole cell ethoxyresorufin-O-deethylase activity, lowering CYP1A1 mRNA levels as well as promoter activity as assessed by transient transfection assays. These negative effects are observed at both the basal and tetrachlorodibenzo-p-dioxin-induced levels. Under the same conditions, CYP1B1 mRNA levels and promoter activity are not affected. The effects on mRNA-induced levels are also observed in another mammary cell line, T47D, but not in mammary cell lines that do not express aryl hydrocarbon receptor and estrogen receptor (ER). Moreover, the use of ER antagonists shows that these effects are ER dependent in MCF-7 cells. In human hepatoma HepG2 cells, which lack functional ER, alpha-endosulfan, but not 17beta-estradiol, displays a repressive effect on CYP1A1 through a different mechanism. These results show that xenoestrogens, by altering the ratio of CYP1B1/CYP1A1, could redirect estradiol metabolism in a more toxic pathway in the breast cell line MCF-7.


Subject(s)
Aryl Hydrocarbon Hydroxylases , Breast Neoplasms/enzymology , Cytochrome P-450 CYP1A1/genetics , Cytochrome P-450 Enzyme System/genetics , Endosulfan/toxicity , Gene Expression Regulation, Enzymologic/drug effects , Hydrocarbons, Chlorinated , Insecticides/toxicity , Polychlorinated Dibenzodioxins/toxicity , Breast Neoplasms/genetics , Cytochrome P-450 CYP1A1/antagonists & inhibitors , Cytochrome P-450 CYP1A1/biosynthesis , Cytochrome P-450 CYP1B1 , Cytochrome P-450 Enzyme System/biosynthesis , Estradiol/toxicity , Gene Expression Regulation, Neoplastic/drug effects , Humans , Kinetics , Promoter Regions, Genetic/drug effects , RNA, Messenger/antagonists & inhibitors , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Aryl Hydrocarbon/physiology , Receptors, Estrogen/antagonists & inhibitors , Receptors, Estrogen/physiology , Tumor Cells, Cultured
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