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Identification of gene signatures for invasive colorectal tumor cells.

Identification of gene signatures for invasive colorectal tumor cells. Research Abstract Details 

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  • Identification of gene signatures for invasive colorectal tumor cells. Abstract Text:

    anja h wieseAnja H Wiese,johannes auerJohannes Auer,silke lassmannSilke Lassmann, ,robert rosenbergRobert Rosenberg,heinz Heinz , ,martin wernerMartin Werner,anja h wieseAnja H Wiese,johannes auerJohannes Auer,silke lassmannSilke Lassmann, ,robert rosenbergRobert Rosenberg,heinz Heinz , ,martin wernerMartin Werner,anja h wieseAnja H Wiese,johannes auerJohannes Auer,silke lassmannSilke Lassmann,jörg nährigJörg Nährig,robert rosenbergRobert Rosenberg,heinz höflerHeinz Höfler,rüdiger rügerRüdiger Rüger,martin wernerMartin Werner,

    Background: Gene signatures of sporadic colorectal carcinoma tissues and microdissected colorectal tumor cells were analyzed to identify stromal and tumor cell-specific markers, respectively. Methods: Serial sections of frozen colorectal tumors (n=29) were subjected to RNA isolation of (1) entire tissue sections with a various tumor cell content and of (2) microdissected invasive tumor cells. Three matching samples of microdissected normal colorectal epithelial and invasive tumor cells were similarly obtained. RNA samples were analyzed using the HG95A and HG95Av2 GeneChip((R)) microarrays (Affymetrix). The microarray data was evaluated by established methods and validated by Q-RT-PCR. Results: Unsupervised hierarchical cluster analysis of 18 sample pairs (training set) clearly distinguished tumors from microdissected tumor cells. A 149-gene signature was identified using statistical methods, which was then validated by a hierarchical clustering analysis of 11 independent sample pairs (test set). Genes specifically associated with microdissected invasive tumor cells were for example CKS2 and NME1. In contrast, genes associated with stromal cells were for example MMP2, SDF1 and FBLN2. Finally, a 65-gene signature distinguished normal colorectal epithelial cells and invasive tumor cells, including down-regulation of BMP2 and ANPEP mRNA expression as well as up-regulation of TKT, SPARC, MCM5 mRNA expression. Conclusions: Our approach allowed precise evaluation of molecular signatures in morphologically defined cell populations and identified novel target genes related to stroma-tumor interactions in colorectal cancer. The approach enables further analysis of gene signatures in different tumor areas and cell types, such as within invasive margins to decipher molecular mechanisms of colorectal cancer invasion and metastasis.

    Identification of gene signatures for invasive colorectal tumor cells. Publishing Authors By Initials

    ah wieseAH Wiese,j auerJ Auer,s lassmannS Lassmann,j J ,r rosenbergR Rosenberg,h H ,r R ,m wernerM Werner,ah wieseAH Wiese,j auerJ Auer,s lassmannS Lassmann,j J ,r rosenbergR Rosenberg,h H ,r R ,m wernerM Werner,ah wieseAH Wiese,j auerJ Auer,s lassmannS Lassmann,j nährigJ Nährig,r rosenbergR Rosenberg,h höflerH Höfler,r rügerR Rüger,m wernerM Werner,

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    Identification of gene signatures for invasive colorectal tumor cells. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Cancer detection and prevention

    VOLUME: 31

    Page Numbers: 282-95

    Journal Abbreviation: Cancer Detect. Prev.

    ISSN: 0361-090X

    DAY: 22

    MONTH: 10

    YEAR: 2007

    Identification of gene signatures for invasive colorectal tumor cells. Information

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    LANGUAGE: eng

    NlmUniqueID: 7704778

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    AFFILIATION: Institut für Allgemeine Pathologie und Pathologische Anatomie, Klinikum rechts der Isar, Technische Universität München, München, Germany; Roche Diagnostics GmbH, Penzberg, Germany.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Cancer Detect Prev

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