TOXIC HALOGENATED AROMATICS
TOXIC HALOGENATED AROMATICS
批准号:
5211190
负责人:
STEPHEN H SAFE
金额:
$0.0万
依托单位:
--
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
MCF7 cell SDS polyacrylamide gel electrophoresis bioassay carbopolycyclic compound chemical structure function clone cells dioxins environmental contamination environmental toxicology enzyme induction /repression estrogen receptors genetic regulatory element halobiphenyl /halotriphenyl compound halohydrocarbon hormone regulation /control mechanism immunotoxicity industrial waste laboratory mouse laboratory rat naphthalenes polychlorodibenzofuran receptor binding receptor expression tissue /cell culture toxicant screening
中文摘要
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英文摘要
Description: This project proposes to conduct several interrelated
studies with individual polycyclic aromatic hydrocarbons (PAHs) and
reconstituted PAH mixtures to determine the interactions of these
compounds and the role of these interactions in PAH-induced
carcinogenicity. The classes of PAH compounds to be studied include the
polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins
(PCDDs) and the polychlorinated dibenzofurans (PCDFs). The proposed
studies include: (1) analysis of the comparative induction of CYP1A1
and CYP1A2 gene expression by a reconstituted PAH mixture and the 2-,3-
and > 4-ring PAH fractions to determine the relative contributions of
the different fractions to the overall induction potency of the mixture;
(2) extension of (1) to include other Ah receptor-mediated responses;
(3) investigation of the selective induction of CYP1A2 by acenaphthylene
with regard to its toxicologic and carcinogenic significance; and (4)
investigation of the interactions of strong carcinogens that are poor
microsomal P450 enzyme inducers and weak carcinogens that are potent
microsomal P450 enzyme inducers. The results obtained will determine the
extent of the non-additive interactions between PCBs and PCDDs/PCDFs and
provide critical data which can be used to evaluate the utility of the
TEF model for risk assessment of HAHs.
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