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- W2411680894 abstract "Objective To investigate the effects of Hic-5/ARA55 on the growth of the human colorectal cancer cells(Lovo cells)and its mechanism.Method Flow cytometry(FCM)was used to study the cell cycle of Lovo cells(Lovo group),Lovo cells stably transfected with empty vector(Lovo-Vector group)and the Lovo cells stably transfected with vector containing Hic-5/ARA55(Lovo-Hic-5/ARA55group).Western blot assay was used to detect the principal cyclins in the three groups,and Luciferase assay was used to study the mechanism between Hic-5/ARA55 and the only target cyclin. The cells from the three groups were inoculated subcutaneously into 7 nude micef Babl/c nu/nu)respectively to observe the effects of Hic-5/ARA55 on the growth of the cells in vivo.Seven weeks later,the subcutaneous tumors were harvested and weighed.Then immunohistochemistrical assay was used to detect Hic-5/ARA55 and the target cyclin in the tumors.Results The cell cycle was obviously delayed from G0/G1 to S stage in Lovo-Hic-5/ARA55 cells.A significantly higher expression of P27 was found in Lovo-Hic-5/ARA55 cells than in the other two groups.The weight of the subcutaneous tumors of Lovo-Hic-5/ARA55 cells,Lovo cells and Lovo-Vector cells were(0.33±0.23)g,(1.20±0.39)g and(1.30 ±0.49)g,respectively;the tumors of Lovo-Hic-5/ARA55 cells was significantly lighter than those ofthe other two groups(P<0.05).Hic-5/ARA55 and P27 were beth over-expressed in implanted tumors of Lovo-Hic-5/ARA55 cells,while were both expressed lower or not expressed in the other two groups.And the expressions of Hic-5/ARA55 and P27 were highly positive correlated(r=0.816,P<0.05).Conclusion Hic-5/ARA55 could inhibit the growth of Lovo cells both in vitro and in vlvo bv up-regulating the transcription of P27.Key words: Colorectal neoplasms; Tumor growth; Hic-5/ARA55; P27" @default.
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- W2411680894 date "2008-06-01" @default.
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- W2411680894 title "[Hic-5/ARA55 inhibits the growth of Lovo cells by up-regulating the expression of P27]." @default.
- W2411680894 doi "https://doi.org/10.3321/j.issn:0529-5815.2008.11.013" @default.
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