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前列腺素脱氢酶对大肠癌SW480细胞恶性增殖的抑制作用[J]. 肿瘤防治研究, 2008, 35(04): 236-239. DOI: 10.3971/j.issn.1000-8578.1399
引用本文: 前列腺素脱氢酶对大肠癌SW480细胞恶性增殖的抑制作用[J]. 肿瘤防治研究, 2008, 35(04): 236-239. DOI: 10.3971/j.issn.1000-8578.1399
Inhibitory Effects of 15-Hydroxyprostaglandin Dehydrogenase on Proliferation of Human Colorectal Cancer Cell SW480[J]. Cancer Research on Prevention and Treatment, 2008, 35(04): 236-239. DOI: 10.3971/j.issn.1000-8578.1399
Citation: Inhibitory Effects of 15-Hydroxyprostaglandin Dehydrogenase on Proliferation of Human Colorectal Cancer Cell SW480[J]. Cancer Research on Prevention and Treatment, 2008, 35(04): 236-239. DOI: 10.3971/j.issn.1000-8578.1399

前列腺素脱氢酶对大肠癌SW480细胞恶性增殖的抑制作用

Inhibitory Effects of 15-Hydroxyprostaglandin Dehydrogenase on Proliferation of Human Colorectal Cancer Cell SW480

  • 摘要: 目的研究15-羟基前列腺素脱氢酶(15-hydroxyprostaglandin dehydrogenase,PGDH)对SW480大肠癌细胞恶性增殖的抑制作用及机制。方法构建PGDH真核表达质粒(pcDNA3.1-PG-DH),在大肠癌SW480细胞中转染并表达PGDH蛋白,采用MTT法、平板集落和软琼脂克隆形成实验,分析PGDH对SW480恶性增殖的影响。Westernblot检测p53、p21蛋白表达改变情况。结果转染表达PGDH后,细胞增殖受到抑制,实验组平板集落形成率为16%,而对照组为58%,两者间差异显著(P<0.05);肿瘤细胞的停泊-非依赖能力降低,实验组软琼脂克隆体积小且形成个数(7±1.68)明显少于对照组(16.3±3.63),差异显著(P<0.05)。Westernblot分析表明,转染表达PGDH后伴随着p53、p21蛋白表达升高。结论转染表达PGDH蛋白能够部分逆转大肠癌SW480细胞的恶性表型,其过程可能与p53、p21通路密切相关。

     

    Abstract: Objective This study investigated the inhibitory effects of 15-hydroxyprostaglandin dehydrogenase gene(PGDH) on the proliferation of SW480 colorectal cancer cells. Methods Recombinant plasmid pcDNA3.1-PGDH with PGDH open reading frame was constructed.The SW480 cells were transfected with either pcDNA3.1 or pcDNA3.1-PGDH using LipofectaminTM 2000.The cell growth kinetics and the ability of proliferation in vitro were detected by MTT and colony formation assay.Flow cytometry was applied to analyze the cell cycle. The expression of PGDH protein and the variation of p53 and p21 were detected in SW480 cells were examined by Western blot . Results  The plasmid of pcDNA 3. 12 PGDH was successfully established. After being t ransfected with this gene, the growth velocity of these t ransfected cells was significantly slower than the parental cell line. Colony formation activity of SW480/pcDNA 3. 12PGDH was 16 % while that of the cont rol cell was 58 % in six well plate ( P < 0. 05) . The activity of anchorage2independent proliferation of SW480/ pcDNA 3. 1 PGDH was lower than that of SW480/ pcDNA 3. 1 in soft agar. Otherwise, the expression of p53 and p21 were higher than cont rol. Conclusion  PGDH could reduce the abilities of proliferation and of anchorage2independent proliferation of SW480 cells which is through p53 pathway possibility.

     

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