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REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells.

REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Research Abstract Details 

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  • REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Abstract Text:

    akira sekikawaAkira Sekikawa,hirokazu fukuiHirokazu Fukui,shigehiko fujiiShigehiko Fujii,kazuhito ichikawaKazuhito Ichikawa,shigeki tomitaShigeki Tomita,johji imuraJohji Imura,tsutomu chibaTsutomu Chiba,takahiro fujimoriTakahiro Fujimori,akira sekikawaAkira Sekikawa,hirokazu fukuiHirokazu Fukui,shigehiko fujiiShigehiko Fujii,kazuhito ichikawaKazuhito Ichikawa,shigeki tomitaShigeki Tomita,johji imuraJohji Imura,tsutomu chibaTsutomu Chiba,takahiro fujimoriTakahiro Fujimori,

    Signal transducer and activator of transcription 3 (STAT3) signaling plays roles in inflammation-associated carcinogenesis. Regenerating gene (REG) Ialpha protein, an interleukin (IL)-6-inducible gene, is suggested to be involved in the gastritis-gastric cancer sequence. We investigated the involvement of IL-6/STAT3 signaling in REG Ialpha protein expression and examined whether REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. The effects of IL-6/STAT3 signaling on REG Ialpha protein expression were examined using a STAT3 small interfering RNA system in gastric cancer cells. The element responsible for IL-6-induced REG Ialpha promoter activation was determined by a promoter deletion assay. The anti-apoptotic effects of STAT3 signaling and its induced REG Ialpha protein were examined by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphatase nick-end labeling and caspase assay in vitro. Human gastric cancer specimens were analyzed by immunohistochemistry for phosphorylated signal transducer and activator of transcription 3 (p-STAT3) and REG Ialpha protein. IL-6 treatment enhanced the expression of REG Ialpha protein through STAT3 activation in gastric cancer cells. The IL-6-responsive element was determined to lie in the sequence from -142 to -134 of the REG Ialpha promoter region. REG Ialpha protein mediated the anti-apoptotic effects of STAT3 signaling in gastric cancer cells by enhancing Akt activation, Bad phosphorylation and Bcl-xL expression. The expression of REG Ialpha protein was significantly correlated with that of p-STAT3 in gastric cancer tissues. REG Ialpha protein may play a pivotal role in anti-apoptosis in gastric tumorigenesis under STAT3 activation.

    REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Publishing Authors By Initials

    a sekikawaA Sekikawa,h fukuiH Fukui,s fujiiS Fujii,k ichikawaK Ichikawa,s tomitaS Tomita,j imuraJ Imura,t chibaT Chiba,t fujimoriT Fujimori,a sekikawaA Sekikawa,h fukuiH Fukui,s fujiiS Fujii,k ichikawaK Ichikawa,s tomitaS Tomita,j imuraJ Imura,t chibaT Chiba,t fujimoriT Fujimori,

    For similar abstracts research abstracts see: abstracts research

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    REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Journal Published:

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

    Journal: Carcinogenesis

    VOLUME: 29

    Page Numbers: 76-83

    Journal Abbreviation: Carcinogenesis

    ISSN: 1460-2180

    DAY: 16

    MONTH: 11

    YEAR: 2007

    REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Information

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    LANGUAGE: eng

    NlmUniqueID: 8008055

    REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells. Keywords Mesh Terms:

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    Grant and Affiliation Information for REG Ialpha protein mediates an anti-apoptotic effect of STAT3 signaling in gastric cancer cells.

    AFFILIATION: Department of Surgical and Molecular Pathology, Dokkyo University School of Medicine 880 Kitakobayshi, Mibu, Shimotsuga, Tochigi 321-0293, Japan.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Carcinogenesis

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