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下调 c-Myc 表达抑制胆管癌细胞的侵袭。

Down-regulation of c-Myc expression inhibits the invasion of bile duct carcinoma cells.

机构信息

Department of Hepatobiliary Surgery, Hainan Provincial Peoples Hospital, Haikou 570311, Peoples Republic of China.

出版信息

Cell Biol Int. 2011 Aug;35(8):799-802. doi: 10.1042/CBI20110099.

Abstract

Cholangiocarcinoma is the second most common primary hepatic tumour originating from biliary tract epithelial cells with poor prognosis. Enhanced c-Myc protein expression contributes to many aspects of tumour cell biology. Although the ability of c-Myc to drive unrestricted cell proliferation and to inhibit cell differentiation had been well recognized, whether down-regulated c-Myc expression can inhibit tumour cell invasion still remains to be explored. The c-Myc ASODN (antisense oligodeoxyribonucleotide) and NSODN (nonsense oligodeoxyribonucleotide) were designed, synthesized and transfected into human QBC939 bile duct carcinoma cells using the Lipofectamine 2000 reagent. The protein expression of c-Myc was detected by Western blot. A transwell experiment was applied to evaluate the invasive capacity of the QBC939 cells. c-Myc ASODN could significantly suppress the c-Myc protein expression (P<0.05) and the invasion (P<0.01) of QBC939 cells transfected with c-Myc ASODN compared with that in the control and c-Myc NSODN-transfected group. Thus in the present study we show that down-regulation of c-Myc expression can inhibit the invasion of QBC939 cells in vitro.

摘要

胆管癌是第二常见的原发性肝肿瘤,源自胆道上皮细胞,预后不良。增强的 c-Myc 蛋白表达有助于肿瘤细胞生物学的许多方面。虽然 c-Myc 驱动无限制的细胞增殖和抑制细胞分化的能力已经得到很好的认识,但下调 c-Myc 表达是否能抑制肿瘤细胞侵袭仍有待探索。设计、合成了 c-Myc ASODN(反义寡脱氧核苷酸)和 NSODN(无意义寡脱氧核苷酸),并使用 Lipofectamine 2000 试剂转染到人 QBC939 胆管癌细胞中。通过 Western blot 检测 c-Myc 的蛋白表达。通过 Transwell 实验评估 QBC939 细胞的侵袭能力。与对照组和转染 c-Myc NSODN 的组相比,c-Myc ASODN 可显著抑制转染 c-Myc ASODN 的 QBC939 细胞的 c-Myc 蛋白表达(P<0.05)和侵袭(P<0.01)。因此,在本研究中,我们表明下调 c-Myc 表达可以抑制 QBC939 细胞在体外的侵袭。

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