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hL RH-1 调控结肠腺癌细胞SW480 增殖的分子机制[J]. 肿瘤防治研究, 2007, 34(12): 904-907. DOI: 10.3971/j.issn.1000-8578.1695
引用本文: hL RH-1 调控结肠腺癌细胞SW480 增殖的分子机制[J]. 肿瘤防治研究, 2007, 34(12): 904-907. DOI: 10.3971/j.issn.1000-8578.1695
Molecular Mechanism of hLRH-1 in Regulating Proliferation of Colon Adenocarcinoma Cells SW480[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 904-907. DOI: 10.3971/j.issn.1000-8578.1695
Citation: Molecular Mechanism of hLRH-1 in Regulating Proliferation of Colon Adenocarcinoma Cells SW480[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 904-907. DOI: 10.3971/j.issn.1000-8578.1695

hL RH-1 调控结肠腺癌细胞SW480 增殖的分子机制

Molecular Mechanism of hLRH-1 in Regulating Proliferation of Colon Adenocarcinoma Cells SW480

  • 摘要: 目的 初步探讨人核受体hLRH-1在结肠癌发生发展中可能的生物学功能。方法 真核表达质粒pcDNA3-hLRH-1经脂质体介导转入SW480细胞中,RT-PCR和Western blot法分别检测外源基因mRNA及蛋白水平的表达;M1vr法分析hLRH-1过表达对SW480细胞生长增殖的影响,同时行实时定量RT-PCR法分析细胞生长增殖相关基因CyclinE1和CyclinD1、以及凋亡调控相关基因Pten和Rb1的表达。结果 hLRH-1过表达的SW480细胞增殖速度明显加快,同时其CyclinE1基因的表达显著增高,而Pten和Rb1在hLRH-1过表达的SW480细胞中均呈明显的表达下调。结论 外源hLRH-1的表达既通过上调CyclinE1基因的表达而促进SW480细胞增殖,还可能通过调节Pten和Rb1基因的表达而参与细胞凋亡的调控。

     

    Abstract: Objective  To explore the possible biological function of human nuclear receptor hLRH-1 in tumorigenesis and progress of colon cancer. Methods  Plasmids pcDNA3-hLRH-1 were int roduced into SW480 cells via lipofectamine. The expression of mRNA and protein of exogenous hLRH-1 was detected by RT-PCR and Western blotting, respectively. MTT assay was carried out to survey the proliferation of SW480 cells with overexpression of hLRH-1. Meanwhile, the expression of proliferation-related genes cyclin E1 and cyclin D1, and apoptosis-related genes PTEN and Rb1, were analyzed by real-time RT-PCR. Results  The proliferation of SW480 cells were promoted under the condition of overexpression of hLRH-1. The expression of cyclin E1 was up-regulated significantly, while that of Pten and Rb1 was down-regulated in SW480 cells with overexpressed hLRH-1. Conclusion  The expression of exogenous hLRH-1 in SW480 cells induced the proliferation resulting form up-regulation of cyclin E1, as well as participated in the regulation of apoptosis via influencing the expression of Pten and Rb1.

     

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