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Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells.

Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Research Abstract Details 

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  • Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Abstract Text:

    susanne heimerlSusanne Heimerl,anja k bosserhoffAnja K Bosserhoff,thomas langmannThomas Langmann,josef eckerJosef Ecker,gerd schmitzGerd Schmitz,

    ATP-binding cassette (ABC) transporters regulate the transport of a variety of physiologic substrates. Moreover, several human ABC proteins are responsible for drug exclusion in compound-treated tumor cells, providing cellular mechanisms for the development of multidrug resistance and, therefore, playing an important role in malignant transformation. As only limited information exists on the role of ABC transporters in melanoma, the aim of the study was to generate a complete expression profile of ABC transporters in this tumor entity. Using a TaqMan low-density array for 47 human ABC transporters, mRNA expression analysis was performed from normal human epidermal melanocytes (NHEM P2 and NHEM P3), nine different cell lines originating from primary melanoma (Mel Ei, Mel Juso, Mel Ho and Mel Wei), and metastases of malignant melanoma (Mel Im, Mel Ju, SK Mel 28, HTZ 19 and HMB2). Cell line-specific expression levels were compared with gene expression in pooled RNA from a variety of other human tissues. High expression levels were detected in pooled tissue RNA as well as in cells of melanocytic origin for ABCA5, ABCB2, ABCB6, ABCD3, ABCD4, ABCF1, ABCF2 and ABCF3, whereas ABCB5 revealed a melanocyte-specific high transcript level. In relation to normal melanocytes, ABCB3, ABCB6, ABCC2, ABCC4, ABCE1 and ABCF2 were significantly increased in melanoma cell lines, whereas ABCA7, ABCA12, ABCB2, ABCB4, ABCB5 and ABCD1 showed lower expression levels. In summary, we present here for the first time an ABC-transporter mRNA expression profile in melanoma in comparison to normal melanocytes. The differentially regulated ABC transporters detected by our approach may be candidate genes involved in melanoma tumorigenesis, progression and therapy resistance and could therefore be of great importance to identify novel options for melanoma therapy.

    Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Publishing Authors By Initials

    s heimerlS Heimerl,ak bosserhoffAK Bosserhoff,t langmannT Langmann,j eckerJ Ecker,g schmitzG Schmitz,

    For similar biological factors: biological markers: tumor markers, biological research abstracts see: biological factors: biological markers: tumor markers, biological research

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    Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Melanoma research

    VOLUME: 17

    Page Numbers: 265-73

    Journal Abbreviation: Melanoma Res.

    ISSN: 0960-8931

    DAY: 19

    MONTH: Oct

    YEAR: 2007

    Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9109623

    Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Keywords Mesh Terms:

    KEYWORDS: Tumor Markers, Biological

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells. Information

    Substance Name: Tumor Markers, Biological

    Registry Number: 0

    Grant and Affiliation Information for Mapping ATP-binding cassette transporter gene expression profiles in melanocytes and melanoma cells.

    AFFILIATION: Institute of Clinical Chemistry, University of Regensburg, Regensburg, Germany.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Melanoma Res

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