國家衛生研究院 NHRI:Item 3990099045/1494
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/1494


    Title: Tumor cell cycle arrest induced by shear stress: Roles of integrins and Smad
    Authors: Chang, SF;Chang, CA;Lee, DY;Leet, PL;Yeh, YM;Yeh, CR;Cheng, CK;Chien, S;Chiu, JJ
    Contributors: Division of Medical Engineering Research
    Abstract: interstitial flow in and around tumor tissue affects the mechanical microenvironment to modulate tumor cell growth and metastasis. We investigated the roles of flow-induced shear stress in modulating cell cycle distribution in four tumor cell lines and the underlying mechanisms. In all four cell lines, incubation under static conditions for 24 or 48 h led to G(0)/G(1) arrest; in contrast, shear stress (12 dyneS/cm(2)) induced G(2)/M arrest. The molecular basis of the shear effect was analyzed, and the presentation on molecular mechanism is focused on human MG63 osteosarcoma cells. Shear stress induced increased expressions of cyclin 11311 and p21(CIP1) and decreased expressions of cyclins A, D1, and E, cyclin-dependent protein kinases (Cdk)-1, -2, -4, and -6, and p27(KIP1) as well as a decrease in Cdk1 activity. Using specific antibodies and small interfering RNA, we found that the shear-induced G2/M arrest and corresponding changes in G2/M regulatory protein expression and activity were mediated by alpha(v)beta(3) and beta(1), integrins through bone morphogenetic protein receptor type IA-specific Smad1 and Smad5. Shear stress also down-regulated runt-related transcription factor 2 (Runx2) binding activity and osteocalcin and alkaline phosphatase expressions in MG63 cells; these responses were mediated by alpha(v)beta(3) and beta(1), integrins through Smad5. Our findings provide insights into the mechanism by which shear stress induces G(2)/M arrest in tumor cells and inhibits cell differentiation and demonstrate the importance of mechanical microenvironment in modulating molecular signaling, gene expression, cell cycle, and functions in tumor cells.
    Keywords: Multidisciplinary Sciences
    Date: 2008-03-11
    Relation: Proceedings of the National Academy of Sciences of the United States of America. 2008 Mar;105(10):3927-3932.
    Link to: http://dx.doi.org/10.1073/pnas.0712353105
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0027-8424&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000253930600049
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=41649091020
    Appears in Collections:[Jeng-Jiann Chiu] Periodical Articles

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