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Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice.

Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Research Abstract Details 

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  • Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Abstract Text:

    takeru oyamaTakeru Oyama,yasuhiro yamadaYasuhiro Yamada,kazuya hataKazuya Hata,hiroyuki tomitaHiroyuki Tomita,akihiro hirataAkihiro Hirata,hongqiang shengHongqiang Sheng,akira haraAkira Hara,hitomi aokiHitomi Aoki,takahiro kunisadaTakahiro Kunisada,satoshi yamashitaSatoshi Yamashita,hideki moriHideki Mori,

    Apc(Min/+) mouse, a mouse model for human familial adenomatosis polyposis, contains a truncating mutation in the Apc gene and spontaneously develops intestinal tumors. Our previous study revealed two distinct stages of tumorigenesis in the colon of Apc(Min/+) mouse: microadenomas and macroscopic tumors. Microadenomas already have lost their remaining allele of the Apc and all microadenomas show accumulation of beta-catenin, indicating that activation of the canonical Wnt pathway is an initiating event in the tumorigenesis. This study shows that expression of nuclear beta-catenin in macroscopic tumors is further upregulated in comparison with that in microadenomas. Furthermore, transcriptional activity of beta-catenin/T-cell factor (Tcf) signaling, assessed using beta-catenin/Tcf reporter transgenic mice, is higher in the macroscopic tumors than that in microadenomas. In addition, the expression level of Dickkopf-1, which is known to be a negative modifier of the canonical Wnt pathway, was reduced only in colon tumors. These results suggest that activation of beta-catenin/Tcf transcription plays a role not only in the initiation stage but also in the promotion stage of colon carcinogenesis in Apc(Min/+) mice.

    Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Publishing Authors By Initials

    t oyamaT Oyama,y yamadaY Yamada,k hataK Hata,h tomitaH Tomita,a hirataA Hirata,h shengH Sheng,a haraA Hara,h aokiH Aoki,t kunisadaT Kunisada,s yamashitaS Yamashita,h moriH Mori,

    For similar abstracts research abstracts see: abstracts research

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    Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Journal Published:

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

    Journal: Carcinogenesis

    VOLUME: 29

    Page Numbers: 666-72

    Journal Abbreviation:

    ISSN: 1460-2180

    DAY: 19

    MONTH: 01

    YEAR: 2008

    Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Information

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    LANGUAGE: eng

    NlmUniqueID: 8008055

    Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice. Keywords Mesh Terms:

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    Grant and Affiliation Information for Further upregulation of beta-catenin/Tcf transcription is involved in the development of macroscopic tumors in the colon of ApcMin/+ mice.

    AFFILIATION: Department of Tumor Pathology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu 501-1194, Japan.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Carcinogenesis

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