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Construction of a recombinant eukaryotic expression vector containing DNM3 gene and its expression in colon cancer cells

机译:含DNM3基因的重组真核表达载体的构建及其在结肠癌细胞中的表达

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Introduction: Dynamin 3 (DNM3) is a large GTPase that possesses mechanochemical properties and has been shown to be involved in malignancies. However, most studies about DNM3 are observational, and knowledge of the precise molecular mechanism of DNM3 remains limited. Materials and methods: We constructed a PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3 recombinant eukaryotic expression vector, which was then transfected into SW620 and LoVo cells. One cell line was divided into three groups. DNM3 mRNA and protein expression was analyzed by quantitative real-time PCR and Western blot assay. To investigate DNM3 biological activity in colon cancer SW620 and LoVo cell line, we performed cell proliferation, transwell migration, and invasion assay. Matrix metalloproteinase (MMP)-2 and MMP-9 protein expressions were detected by Western blot. Result: We successfully constructed a PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3 recombinant eukaryotic expression vector, and stable DNM3 expression was observed in SW620 and LoVo cell lines. The vector overexpressing DNM3 inhibited the proliferation, weak invasion, and migration ability of colon cancer SW620 and LoVo cells relative to those in the control group (all P 0.001). DNM3 downregulated the protein expression of MMP-2 and MMP-9. Conclusion: DNM3 may weaken the malignant behavior of colon cancer and may have promoted the invasion and migration of colon cancer by regulating the expression of MMP-2 and MMP-9.
机译:简介:Dynamin 3(DNM3)是一种大型GTPase,具有机械化学性质,已被证明与恶性肿瘤有关。但是,有关DNM3的大多数研究都是观察性的,对DNM3的确切分子机制的知识仍然有限。材料和方法:我们构建了PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3重组真核表达载体,然后将其转染到SW620和LoVo细胞中。将一个细胞系分为三组。 DNM3 mRNA和蛋白表达通过定量实时PCR和Western印迹分析进行了分析。为了研究结肠癌SW620和LoVo细胞系中DNM3的生物学活性,我们进行了细胞增殖,跨孔迁移和侵袭分析。 Western blot检测基质金属蛋白酶(MMP)-2和MMP-9蛋白的表达。结果:成功构建了PCDH-CMV-MCS-EF1a-GFP-Puro-DNM3重组真核表达载体,在SW620和LoVo细胞株中观察到稳定的DNM3表达。相对于对照组,过表达DNM3的载体抑制结肠癌SW620和LoVo细胞的增殖,弱侵袭和迁移能力(所有P <0.001)。 DNM3下调MMP-2和MMP-9的蛋白表达。结论:DNM3可能通过调节MMP-2和MMP-9的表达而减弱结肠癌的恶性行为,并可能促进结肠癌的侵袭和迁移。

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