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Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells.

Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Research Abstract Details 

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  • Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Abstract Text:

    sandra s wiseSandra S Wise,amie l holmesAmie L Holmes,john pierce wiseJohn Pierce Wise,

    Particulate hexavalent chromium (Cr(VI)) is a well-established human lung carcinogen. It is currently a major public health concern, there is widespread exposure to it in occupational settings and to the general public. However, despite the potential widespread exposure and the fact that the lung is its target organ, few studies have considered the toxic effects of particulate Cr(VI) in human lung cells. Accordingly, we used lead chromate as a model particulate Cr(VI) compound and determined its cytotoxicity and genotoxicity in cultured human bronchial epithelial cells, using BEP2D cells as a model cell line. We found that lead chromate induced concentration-dependent cytotoxicity in BEP2D cells after a 24h exposure. Specifically, the relative survival was 78, 59, 53, 46 and 0% after exposure to 0.5, 1, 5, 10 and 50 microg/cm(2) lead chromate, respectively. Similarly, the amount of chromosome damage increased with concentration after 24h exposure to lead chromate. Specifically, 0.5, 1, 5 and 10 microg/cm(2) damaged 10, 13, 20 and 28% of metaphase cells with the total amount of damage reaching 11, 15, 24 and 36 aberrations per 100 metaphases, respectively. Lead chromate (50 microg/cm(2) lead chromate) induced profound cell cycle delay and no metaphases were found. In addition we investigated the effects of soluble hexavalent chromium, sodium chromate, in this cell line. We found that 1, 2.5, 5 and 10 microM sodium chromate induced 66, 35, 0 and 0% relative survival, respectively. The amount of chromosome damage increased with concentration after 24h exposure to sodium chromate. Specifically, 1, 2.5 and 5 microM damaged 25, 34 and 41% of metaphase cells with the total amount of damage reaching 33, 59 and 70 aberrations per 100 metaphases, respectively. Ten micromolar sodium chromate induced profound cell cycle delay and no metaphases were found. Overall the data clearly indicate that hexavalent Cr(VI) is cytotoxic and genotoxic to human lung epithelial cells.

    Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Publishing Authors By Initials

    ss wiseSS Wise,al holmesAL Holmes,jp wiseJP Wise,

    For similar natural sciences: chemistry: chemistry, physical: solubility research abstracts see: natural sciences: chemistry: chemistry, physical: solubility research

    PUBMED ID PMID:

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    Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Mutation research

    VOLUME: 610

    Page Numbers: 2-7

    Journal Abbreviation: Mutat. Res.

    ISSN: 0027-5107

    DAY: 26

    MONTH: 07

    YEAR: 2006

    Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 400763

    Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Keywords Mesh Terms:

    KEYWORDS: Solubility

    MESH TERMS: pharmacology

    Chemical & Substance for Abstract: Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells. Information

    Substance Name: sodium chromate(VI)

    Registry Number: 7775-11-3

    Grant and Affiliation Information for Particulate and soluble hexavalent chromium are cytotoxic and genotoxic to human lung epithelial cells.

    AFFILIATION: Wise Laboratory of Environmental and Genetic Toxicology, Maine Center for Toxicology and Environmental Health, University of Southern Maine, PO Box 9300, Portland, ME 04103-9300, United States.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

    AGENCY: United States NIEHS

    GRANT: ES10838

    ACRONYM: ES

    MEDLINETA: Mutat Res

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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